Ortho substituted chiral phosphines and phosphinites and their use in asymmetric catalytic reactions

Abstract

3,3′-Substituted chiral biaryl phosphine and phosphinite ligands and metal complexes based on such chiral ligands useful in asymmetric catalysis are disclosed. The metal complexes are useful as catalysts in asymmetric reactions, such as, hydrogenation, hydride transfer, allylic alkylation, hydrosilylation, hydroboration, hydrovinylation, hydroformylation, olefin metathesis, hydrocarboxylation, isomerization, cyclopropanation, Diels-Alder reaction, Heck reaction, isomerization, Aldol reaction, Michael addition, epoxidation, kinetic resolution and [m+n] cycloaddition. The metal complexes are particularly effective in Ru-catalyzed asymmetric hydrogenation of beta-ketoesters to beta-hydroxyesters and Ru-catalyzed asymmetric hydrogenation of enamides to beta amino acids.

Description

BACKGROUND OF THE INVENTION

[0002] 1. Field of the Invention

[0003] The present invention relates to novel chiral ligands derived from 3,3′-substituted biaryl phosphines and phosphinites. More particularly, the present invention relates to transition metal complexes of these chiral phosphine ligands. The transition metal complexes are useful as catalysts in asymmetric reactions, such as, hydrogenation, hydride transfer, allylic alkylation, hydrosilylation, hydroboration, hydrovinylation, hydroformylation, olefin metathesis, hydrocarboxylation, isomerization, cyclopropanation, Diels-Alder reaction, Heck reaction, isomerization, Aldol reaction, Michael addition, epoxidation, kinetic resolution and [m+n] cycloaddition.

[0004] 2. Description of the Prior Art

[0005] Discovery of new chiral ligands is crucial in developing highly enantioselective transition metal-catalyzed reactions. Many chiral ligands have been made for applications in asymmetric catalysis, however, relatively few of these chiral ligands are commonly used in industry for the synthesis of chiral molecules.

[0006] Several chiral ligands having a biaryl backbone are known in the prior art. These are summarized below: 1

[0007] Among these ligands, BINAP (1) is one of the most frequently used chiral ligands. The axially dissymmetric, fully aromatic BINAP has demonstrated to be highly effective for many asymmetric reactions (Noyori, R. et al. Acc. Chem. Res. 1990, 23, 345, Ohkuma, T. et al. J. Am. Chem. Soc. 1998, 120, 13529). Recent results show that partially hydrogenated BINAP with a larger bite angle, H8-BINAP (2), is a better ligand for certain asymmetric reactions due to restriction of conformational flexibility (Zhang X. et al. Synlett 1994, 501). Chiral BINAPO (3) was made and it was not effective due to the conformational flexibility (Grubbs, R. et al. Tetrahedron Lett. 1977, 1879). Other axially dissymmetric ligands such as BIPHEMP (4) and MeO-BIPHEP (5) were developed and used for a number of asymmetric reactions (Schmid, R. et al. Pure & Appl. Chem. 1996, 68, 13 1; Schmide, R. et al. Helv. Chim. Acta, 1988, 71, 897). However, the present inventor is not aware of any examples of related 3,3′ substituted chiral biaryl phosphines, the subject of the present invention, being disclosed in the prior art (Broger, E. A. et al., WO 92/16536 and Broger, E. A. et al., WO93/15089). NAPHOS (6), another example of a prior art compound has been prepared (Tamao, K. et al. Tetrahedron Lett. 1977, 1389) and was found to be not effective for asymmetric hydrogenation reaction. The corresponding ligands with the N linker, BDPAB (7) and H8-BDPAB (8) have also been made and tested for asymmetric hydrogenation reactions (Zhang, F. et al. J. Am. Chem. Soc. 1998, 120, 5808).

SUMMARY OF THE INVENTION

[0008] The present invention includes a ligand represented by the formula or its enantiomer: 2

[0009] wherein each X and X′ is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2;

[0010] wherein each Z and Z1 is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2; or wherein Z and Z1 together form the bridging group A-B-A1;

[0011] wherein each Z′, Z″, Z1′ and Z1″ is independently selected from the group consisting of: H, alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2, or wherein Z′ and Z together form the bridging group A′-B-A; Z′ and Z together form a fused cycloaliphatic or aromatic group; Z1 and Z1′ together form the bridging group A1-B1-A1′; and/or Z1 and Z1′ together form a fused cycloaliphatic or aromatic group;

[0012] wherein each A, A′, A1 and A1′ is independently selected from the group consisting of: O, CH2, NH, NR, S, CO and a bond;

[0013] wherein each B and B1 is independently selected from the group consisting of: linear, branched or cyclic alkylene of 1 to 6 carbon atoms, arylene of 6 to 12 carbon atoms, O, CH2, NH, NR, S, CO, SO2, P(O)R, P(O)OR, POR, SiR2 and a bond;

[0014] wherein each T is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, substituted aryl, alkoxide, aryloxide, R, R′, R″, YR′, YR″, Y′R′ and Y″R″; or wherein two T groups together form an alkylene, arylene, alkylenediamino, arylenediamino, alkelenedioxyl or arylenedioxyl;

[0015] wherein each T′ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, substituted aryl, alkoxide, aryloxide, R, R′, R″, YR′, YR″, Y′R′ and Y″R″; or wherein two T′ groups together form an alkylene, arylene, alkylenediamino, arylenediamino, alkelenedioxyl or arylenedioxyl;

[0016] wherein each R, R′ and R″ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, aralkyl and alkaryl of 1 to 22 carbon atoms; or wherein two R groups, two R′ groups or two R″ group together form an alkylene or arelene group; and

[0017] wherein each Y, Y′ and Y″ is independently selected from the group consisting of: O, CH2, NH, S and a bond between carbon and phosphorus; with the proviso that when the Y group at the 2′ position is a bond between carbon and phosphorus, X′ is hydrogen.

[0018] The present invention further includes a catalyst prepared by a process, which includes: contacting a transition metal salt, or a complex thereof, and a ligand according to the present invention.

[0019] The present invention still further includes a process for preparation of an asymmetric compound including: contacting a substrate capable of forming an asymmetric product by an asymmetric reaction and a catalyst prepared by a process including: contacting a transition metal salt, or a complex thereof, and a ligand according to the present invention.

[0020] The metal complexes are useful as catalysts in asymmetric reactions, such as, hydrogenation, hydride transfer, allylic alkylation, hydrosilylation, hydroboration, hydrovinylation, hydroformylation, olefin metathesis, hydrocarboxylation, isomerization, cyclopropanation, Diels-Alder reaction, Heck reaction, isomerization, Aldol reaction, Michael addition, epoxidation, kinetic resolution and [m+n] cycloaddition. The metal complexes are particularly effective in Ru-catalyzed asymmetric hydrogenation of beta-ketoesters to beta-hydroxyesters and Ru-catalyzed asymmetric hydrogenation of enamides to beta amino acids.

DETAILED DESCRIPTION OF THE INVENTION

[0021] The present invention includes 3,3′-substituted chiral biaryl phosphines and phosphinites and related ligands for applications in asymmetric catalysis. Introduction of 3,3′-substituted groups can restrict the rotation of substituents adjacent to the phosphines. Control of orientations of these groups around the phosphine can lead to effective chiral induction for asymmetric reactions. Metal complexes of these phosphines, phosphinites and related non-C2 symmetric ligands with ortho substitution are useful for a large variety of asymmetric reactions. A number of chiral ligands can be made having the desired structure in which the 3,3′ positions are substituted, with the proviso that at least one ortho position is occupied by a group other than H atom.

[0022] In the non-C2 symmetric ligands, ortho substituted groups play an important role for asymmetric catalysis. The 3,3′ substituted chiral biaryl phosphines, phosphinites and related ligands of the present invention are described below. An important feature of these ligands is that at least one of the 3 and 3′ positions must be occupied by a group other than hydrogen.

[0023] The ligands are represented by the formula: 3

[0024] wherein each X and X′ is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2;

[0025] wherein each Z and Z1 is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2; or wherein Z and Z1 together form the bridging group A-B-A1;

[0026] wherein each Z′, Z″, Z1′ and Z1″ is independently selected from the group consisting of: H, alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2 or wherein Z′ and Z together form the bridging group A′-B-A; Z′ and Z together form a fused cycloaliphatic or aromatic group; Z1 and Z1′ together form the bridging group A1-B1-A1′; and/or Z1 and Z1′ together form a fused cycloaliphatic or aromatic group;

[0027] wherein each A, A′, A1 and A1′ is independently selected from the group consisting of: O, CH2, NH, NR, S, CO and a bond;

[0028] wherein each B and B1 is independently selected from the group consisting of: linear, branched or cyclic alkylene of 1 to 6 carbon atoms, arylene of 6 to 12 carbon atoms, O, CH2, NH, NR, S, CO, SO2, P(O)R, P(O)OR, POR, SiR2 and a bond;

[0029] wherein each T is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, substituted aryl, alkoxide, aryloxide, R, R′, R″, YR′, YR″, Y′R′ and Y″R″; or wherein two T groups together form an alkylene, arylene, alkylenediamino, arylenediamino, alkelenedioxyl or arylenedioxyl;

[0030] wherein each T′ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, substituted aryl, alkoxide, aryloxide, R, R′, R″, YR′, YR″, Y′R′ and Y″R″; or wherein two T′ groups together form an alkylene, arylene, alkylenediamino, arylenediamino, alkelenedioxyl or arylenedioxyl;

[0031] wherein each R, R′ and R″ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, aralkyl and alkaryl of 1 to 22 carbon atoms; or wherein two R groups, two R′ groups or two R″ group together form an alkylene or arelene group; and

[0032] wherein each Y, Y′ and Y″ is independently selected from the group consisting of: O, CH2, NH, S and a bond between carbon and phosphorus; with the proviso that when the Y group at the 2′ position is a bond between carbon and phosphorus, X′ is hydrogen. Preferably the alkylene group includes compounds represented by the formula: —(CH2)n—, wherein n is an integer in the range of from 1 to 8. The present invention also includes the corresponding enantiomer of each of the above ligands.

[0033] The substituted alkyl group can have one or more substituents and each substituent can independently be halogen, ester, ketone, carboxylic acid, hydroxy, alkoxy, aryloxy, thiol, alkylthio or dialkylamino. The aryl groups can optionally have one or more substituents, each of which can independently be halogen, ester, ketone, sulfonate, phosphonate, hydroxy, alkoxy, aryloxy, thiol, alkylthiol, nitro, amino, vinyl, substituted vinyl, carboxylic acid, sulfonic acid or phosphine. The arylene groups optionally can have one or more substituents, each of which can independently be halogen, ester, ketone, sulfonate, phosphonate, hydroxy, alkoxy, aryloxy, thiol, alkylthiol, nitro, amino, vinyl, substituted vinyl, carboxylic acid, sulfonic acid or phosphine. Preferably, each of the arylene groups can be 1,2-divalent phenyl, 2,2′-divalent-1,1′-biphenyl, 2,2′-divalent-1,1′-binaphthyl or ferrocene, i.e., a —Fc— group.

[0034] In a preferred embodiment, the present invention includes compounds represented by the following formulas: 4

[0035] wherein each X and X′ is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2;

[0036] wherein each Z and Z1 is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2; or wherein Z and Z1 together form the bridging group A-B-A1;

[0037] wherein each Z′, Z″, Z1′ and Z1″ is independently selected from the group consisting of: H, alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2; or wherein Z′ and Z together form the bridging group A′-B-A; Z′ and Z together form a fused cycloaliphatic or aromatic group; Z1 and Z1′ together form the bridging group A1-B1-A1′; and/or Z1 and Z1′ together form a fused cycloaliphatic or aromatic group;

[0038] wherein each A, A′, A1 and A1′ is independently selected from the group consisting of: O, CH2, NH, NR, S, CO and a bond;

[0039] wherein each B and B1 is independently selected from the group consisting of: linear, branched or cyclic alkylene of 1 to 6 carbon atoms, arylene of 6 to 12 carbon atoms, O, CH2, NH, NR, S, CO, SO2, P(O)R, P(O)OR, POR, SiR2 and a bond;

[0040] wherein each YR′, YR″, Y′R′ and Y″R″ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, substituted aryl, alkoxide and aryloxide; or wherein two YR′, YR″, Y′R′ or Y″R″ groups together form an alkylene, arylene, alkylenediamino, arylenediamino, alkelenedioxyl or arylenedioxyl;

[0041] wherein each R, R′ and R″ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, aralkyl and alkaryl of 1 to 22 carbon atoms; or wherein two R groups, two R′ groups or two R″ group together form an alkylene or arelene group; and

[0042] wherein each Y, Y′ and Y″ is independently selected from the group consisting of: O, CH2, NH, S and a bond between carbon and phosphorus; with the proviso that when the Y group at the 2′ position is a bond between carbon and phosphorus, X′ is hydrogen.

[0043] In another preferred embodiment, the present invention includes compounds represented by the following formulas: 5

[0044] wherein each X is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2;

[0045] wherein each X′ is independently selected from the group consisting of: hydrogen, alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2;

[0046] wherein each Z and Z1 is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2;

[0047] wherein each Z′, Z″, Z1′ and Z1″ is independently selected from the group consisting of: H, alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2;

[0048] wherein each A, A′, A1 and A1′ is independently selected from the group consisting of: O, CH2, NH, NR, S, CO and a bond;

[0049] wherein each B and B1 is independently selected from the group consisting of: linear, branched or cyclic alkylene of 1 to 6 carbon atoms, arylene of 6 to 12 carbon atoms, O, CH2, NH, NR, S, CO, SO2, P(O)R, P(O)OR, POR, SiR2 and a bond;

[0050] wherein each R and R′ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, substituted aryl, aralkyl and alkaryl of 1 to 22 carbon atoms, alkoxide and aryloxide; or

[0051] wherein two R groups or two R′ groups together form an alkylene, arelene, alkylenediamino, arylenediamino, alkelenedioxyl or arylenedioxyl groups.

[0052] The ligands of the present invention can be a racemic mixture of enantiomers. Preferably, the ligand is a non-racemic mixture of enantiomers, and more preferably, the ligand is one of the enantiomers. Preferably, the ligand has an optical purity of at least 85% ee, and more preferably, the ligand has an optical purity of at least 95% ee.

[0053] Selected examples of the chiral ligands according to the present invention are represented by the following formulas: 6

[0054] The present invention also includes a catalyst prepared by a process comprising contacting a transition metal salt, or a complex thereof, and a ligand according to the present invention. The catalyst may be prepared in situ or as an isolated compound.

[0055] The catalyst of the present invention can be a racemic mixture of enantiomers. Preferably, the catalyst is a non-racemic mixture of enantiomers, and more preferably, the catalyst is one of the enantiomers. Preferably, the catalyst has an optical purity of at least 85% ee, and more preferably, the catalyst has an optical purity of at least 95% ee.

[0056] Suitable transition metals for the preparation of the catalyst include Ag, Pt, Pd Rh, Ru, Ir, Cu, Ni, Mo, Ti, V, Re and Mn.

[0057] As mentioned above, the catalyst can be prepared by contacting a transition metal salt or its complex and a ligand according to the present invention.

[0058] Suitable transition metal salts or complexes include the following:

[0059] AgX; Ag(OTf); Ag(OTf)2; AgOAc; PtCl2; H2PtCl4; Pd2(DBA)3; Pd(OAC)2; PdCl2(RCN)2; (Pd(allyl)Cl)2; Pd(PR3)4; (Rh(NBD)2)X; (Rh (NBD)Cl)2; (Rh(COD)Cl)2; (Rh(COD)2)X; Rh(acac)(CO)2; Rh(ethylene)2(acac); (Rh(ethylene)2Cl)2; RhCl(PPh3)3; Rh(CO)2Cl2; RuHX(L)2(diphosphine), RuX2(L)2 (diphosphine), Ru(arene)X2(diphosphine), Ru(aryl group)X2; Ru(RCOO)2(diphosphine); Ru(methallyl)2(diphosphine); Ru(aryl group)X2(PPh3)3; Ru(COD)(COT); Ru(COD)(COT)X; RuX2(cymen); Ru(COD)n; Ru(aryl group)X2(diphosphine); RuCl2(COD); (Ru(COD)2)X; RuX2(diphosphine); RuCl2(═CHR)(PR′3)2; Ru(ArH)Cl2; Ru(COD)(methallyl)2; (Ir(NBD)2Cl)2; (Ir(NBD)2)X; (Ir(COD)2Cl)2; (Ir(COD)2)X; CuX (NCCH3)4; Cu(OTf); Cu(OTf)2; Cu(Ar)X; CuX; Ni(acac)2; NiX2; (Ni(allyl)X)2; Ni(COD)2; MoO2(acac)2; Ti(OiPr)4; VO(acac)2; MeReO3; MnX2 and Mn(acac)2; wherein each R and R′ is independently selected from the group consisting of: alkyl or aryl; Ar is an aryl group; and X is a counteranion.

[0060] In the above transition metal salts and complexes, L is a solvent and the counteranion X can be halogen, BF4, B(Ar)4 wherein Ar is fluorophenyl or 3,5-di-trifluoromethyl-1-phenyl, ClO4, SbF6, PF6, CF3SO3, RCOO or a mixture thereof.

[0061] In another aspect, the present invention includes a process for preparation of an asymmetric compound using the catalysts described above. The process includes the step of contacting a substrate capable of forming an asymmetric product by an asymmetric reaction and a catalyst according to the present invention prepared by contacting a transition metal salt, or a complex thereof, and a ligand according to the present invention.

[0062] Suitable asymmetric reactions include asymmetric hydrogenation, hydride transfer, allylic alkylation, i.e., palladium-catalyzed allylic alkylation of an allylic ester, hydrosilylation, hydroboration, hydrovinylation, hydroformylation, olefin metathesis, hydrocarboxylation, isomerization, cyclopropanation, Diels-Alder reaction, Heck reaction, isomerization, Aldol reaction, Michael addition; epoxidation, kinetic resolution, i.e., palladium-catalyzed allylic alkylation of a racemic allylic ester, and [m+n] cycloaddition wherein m=3 to 6 and n=2, i.e., silver-catalyzed asymmetric [3+2] cycloaddition of an azomethine ylide with a dipolarophile.

[0063] Preferably, the asymmetric reaction is hydrogenation and the substrate to be hydrogenated is an ethylenically unsaturated compound, imine, enamine, enamide, vinyl ester or a ketone, including a ketone such as a beta-ketoester.

[0064] In the case of beta-ketoesters and enamides, the use of Ru as the transition metal to produce an asymmetric beta-hydroxyester and beta amino acid, respectively, is preferred, particularly when the ligand is a compound represented by one of the following formulas: 7

[0065] wherein each R is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl and SiR3; and wherein each Ar is independently selected from the group consisting of: phenyl, substituted phenyl, aryl and substituted aryl; 8

[0066] or a combination thereof.

[0067] The detailed description of ligand synthesis and asymmetric reactions thereof is provided below.

[0068] General Procedures

[0069] All reactions and manipulations were performed in a nitrogen-filled glove box or using standard Schlenk techniques. THF and toluene were dried and distilled from sodium-benzophenone ketyl under nitrogen. Methylene chloride was distilled from CaH2. Methanol was distilled from Mg under nitrogen. (R, R)-BDNPB was made a solution of 10 mg/ml in toluene before use. Column chromatography was performed using EM silica gel 60 (230˜400 mesh). 1H, 13C and 31P NMR were recorded on Bruker WP-200, AM-300, and AMX-360 spectrometers. Chemical shifts were reported in ppm down field from tetramethylsilane with the solvent resonance as the internal standard. Optical rotation was obtained on a Perkin-Elmer 241 polarimeter. MS spectra were recorded on a KRATOS mass spectrometer MS 9/50 for LR-EI and HR-EI. GC analysis was carried on Helwett-Packard 6890 gas chromatography using chiral capillary columns. HPLC analysis was carried on Waters™ 600 chromatography.

[0070] Ligand Synthesis

[0071] Ligand Synthesis

[0072] Several chiral ligands have been prepared and used for asymmetric hydrogenation reactions. Scheme 1 shows the synthesis of these ligands. The starting material, enantiomerically pure BINOL can be converted to many chiral phosphines and phosphinites (11a-L20, 11b-L18, 11c-L31, 11d and 15-L38). 3,3′-disubstituted BINOL was prepared from (S)-BINOL according to known literature methods (Cox, P. J. et al. Tetrahedron Lett. 1992, 33, 2253; Simonsen, K. B. et al. J. Org. Chem. 1998, 63, 7536). 9

[0073] Chiral bisphosphinite ligands (11a-L20, 11b-L18, 11c-L31, 11d) were made through reaction of chlorodiaryl phosphine with the corresponding chiral diols (10a-10c) in high yields. Chiral bisphosphine 15 was made from 3,3′-diphenyl-2,3′dihydroxyl-1,1′-binaphthyl (10b) in a few steps. Compounds 12-14 were synthesized according to a reported procedure (Xiao, D. et al. Org. Lett. 1999, 1, 1679). Representative examples can be synthesized by a variety of methods. Several such methods suitable for use in the synthesis of chiral 3,3′disubstituted bisaryl phosphines, are described below:

Examples of Ligand Synthesis

[0074] 10

EXAMPLE 1

[0075] Synthesis of a 3,3′-Disubstituted Chiral BINOL (10b) 11

[0076] To a THF (200 ml) solution of NaH (5.52 g, 230 mmol) was added (R)-BINOL (28.6 g, 100 mmol) solution in THF (50 ml) under nitrogen at zero temperature, after 30 min, chloromethyl methyl ether (17.09 ml, 225 mmol) in 30 ml THF was added dropwise. The mixture was stirred overnight at room temperature. 3 ml water was added carefully to destroy the excess NaH, and filtered to remove the inorganic salt. The solution was passed a silica gel plug (hexane/ethyl acetate=1/1) to give pure product (97% yield). 12

[0077] To a solution of (R)-2,2′-Bismethoxymethoxy-1,1′-binaphthyl (37.4 g, 100 mmol) in diethyl ether (400 ml) was added n-BuLi (100 ml, 2.5 M in hexane, 250 mmol) at room temperature under nitrogen, the mixture was stirred for 3 hours, then was cooled to 0° C., 200 ml THF was added, after 10 min, a solution of iodine (300 mol, 76.2 g) in THF (60 ml) was added dropwise. The mixture was allowed to warm to room temperature over 4 hours. 100 ml saturated Na2SO3 aqueous was added to destroy the excess iodine, then extracted with ethyl acetate, organic phase was washed with 100 ml saturated Na2SO3, 3×100 ml water, dried over sodium sulfate and evaporated. The residue was purified by a silica gel column eluted with (hexane/ethyl acetate=7/1) to give product as a yellow solid (80% yield, contain 5-7% monoiodo-substituted product). 13

[0078] To a solution of (R)-3,3′-diiodo-2,2′-Bismethoxymethoxy-1,1′-binaphthyl (90 mmol, 56.3 g) and phenylboronic acid (25.2 g, 225 mmol) in THF 800 ml, was added Pd(PPh3)4 (2.3 g, 2 mmol) and degassed 1M K2CO3 aqueous solution (400 ml, 400 mmol). The reaction mixture was heated at reflux for 20 hours. The mixture was extracted with ethyl acetate, and combined organic layer was washed with brine. Evaporation of the solvent gave a yellow solid (47 g). The residue was used to next step without other purification. 14

[0079] (R)-3,3′-diphenyl-1,1′-binaphthol

[0080] To a solution of (R)-3,3′-diphenyl-2,2′-Bismethoxymethoxy-1,1′binaphthyl (47 g) in a mixture solvent of 200 ml DCM and 500 ml EtOH was added concentrated HCl (90 ml). The reaction mixture was heated at reflux under nitrogen for 16 hours. The volatile components were removed under reduced pressure, and the residue was purified by column chromatography on silica gel (DCM/hexanes=4/6) to give the product (25.2 g, 57.6 mmol, 64% yield for two steps)

EXAMPLE 2

[0081] Alternative Route for the Synthesis of a 3,3′-Disubstituted Chiral BINOL (10b)

[0082] (S)-2,2′-Dimethoxy-1,1′-dinaphthyl

[0083] To a solution of (S)-2,2′-dihydroxy-1,1′-dinaphthyl (100 g, 349.7 mmol) in 1000 ml 95% EtOH was added dimethyl sulfate (93.1 ml, 981.7 mmol, 2.8eq.) and followed by dropwise addition of a solution of NaOH (175 g) in 300 ml H2O. After the addition, the resulting system was heated to reflux for 3 h, and then cooled. The reaction mixture was filtered, the precipitate was collected and washed with 10% aqueous NaOH (3×150 ml), and recrystallized from toluene (reflux to dissolve into 700 ml toluene, then let it stay at 0° C. overnight) to yield 84.1 g white crystal product (S)-2,2′-dimethoxy-1,1′-dinaphthyl (yield=76.6%). 1H-NMR (CDCl3):δ7.985(d, J=9.0 Hz, 2H, Ar-H), 7.875(d, J=8.1 Hz, 2H, Ar—H), 7.468(d, J=9.0 Hz, 2H, Ar—H), 7.300 7.326(t, 2H, Ar—H), 7.199 7.218(t, 2H, Ar—H), 7.118(d, J=8.1 Hz, 2H, Ar—H), 3.773(s, 6H, —OCH3).

[0084] (S)-3,3′-Bis(dihydroxyborane)-2,2′-Dimethoxy-1,1′-dinaphthyl

[0085] Under N2, in a 500 ml Schlenk flask were placed 300 ml of dry t-butyl-methyl ether and TMEDA (14.4 ml, 95.5 mmol, 3equiv). To this solution was added 2.5M n-BuLi in hexane(39.5 ml, 98.7 mmol, 3.1 equiv), the resulting solution was stirred for 30 min. at room temperature, solid (S)-2,2′-dimethoxy-1,1′-dinaphthyl (100 g, 31.8 mmol) was added in one portion under N2 flow, the reaction system was stirred at room temperature for 3 hrs. The resulting brown slurry was cooled to −78° C., and B(OEt)3 (33.9 ml, 197.5 mmol, 6.2equiv) was dropwise introduced over a period of 15 min. The reaction system was allowed to warm room temperature and was left stirring overnight. The reaction was quenched with 150 ml aqueous 1M HCl solution, and was stirred for another 2 h. The phase was separated, the organic phase was washed with aqueous 1M HCl solution (3×100 mL) and saturated aqueous NaCl solution (3×100 ml), and dried over Na2SO4. The solvent was removed, and the resulting white solid were recrystallized twice from 70 ml toluene (reflux to dissolve into 700 ml toluene, then let it stay at 0° C. overnight, and recrystallization once can't remove by-product completely) to give the product (S)-3,3′-Bis(dihydroxyborane)-2,2′-Dimethoxy-1,1′-dinaphthyl 9.33 g (Yield =73.3%).1H-NMR(Acetone-d6):δ 8.556(s, 2H, Ar—H), 8.041(d, J=8.1 Hz, 2H, Ar—H), 7.454(t, 2H, Ar—H), 7.335(t, 2H, Ar—H), 7.112(d, J=8.1 Hz, 2H, Ar—H), 3.773(s, 6H, —OCH3). 1H-NMR shows that toluene is very difficult to remove completely, but there is no any influence on the secondary reaction.

[0086] (S)-3,3′-Diphenyl-2,2′-dimethoxy-1,1′-dinaphthyl

[0087] In a 50 ml Schlenk flask were placed (S)-3,3′-bis(dihydroxyborane)-2,2′-dimethoxy-1,1′-dinaphthyl(1.206 g, 3 mmol), Ba(OH)2.8H2O (2.739 g, 8.7 mmol, 2.9 equiv), and Pd(PPh3)4 (183 mg, 0.15 mmol, 5% mol), the reaction system was evacuated and filled with N2 for three times, 1,4-dioxane(18 ml), H2O(8 ml), and bromobenzen(1.89 ml, 18 mmol, 6eq.) were added. The reaction system was heated under reflux for 24 hrs under N2 and cooled to room temperature. The 1,4-dioxane was removed, and the resulting mixture was redissolved into 100 ml CH2Cl2, and washed with aqueous 1M HCl solution (3×50 ml) and saturated aqueous NaCl solution(2×50 ml), and dried over Na2SO4. The solvent was removed to yield crude product (S)-3,3′-diphenyl-2,2′-dimethoxy-1,1′-dinaphthyl 1.513 g as orange G 5 syrup.

[0088] This intermediate was not isolated and was used directly in the final step.

[0089] (S)-3,3′-Diphenyl-2,2′-dihydroxy-1,1′-dinaphthyl (10b)

[0090] The crude product diphenyl-2,2′-dimethoxy-1,1′-dinaphthyl (1.513 g, approximately 3 mmol) was dissolved into 80 ml dry CH2Cl2, and cooled to −78° C., BBr3(1.5 ml) was added in 10 min., and the reaction system was stirred for 18 h at room temperature. The resulting slight brown solution was cooled to 0° C., and 200 ml H2O was added carefully. The phase was separated, and the organic phase was washed with H2O (5×80 ml) and saturated aqueous NaCl solution (2×50 ml), and dried over Na2SO4. The solvent was removed, and the resulting solid was recrystallized from 10 ml MeOH to yield (S)-10b as white-gray powder (overall yield of coupling and deprotection steps, 61.8%).

[0091] 1 H-NMR(CDCl3):δ8.029(s, 2H, Ar—H), 7.929(d, J=7.9 Hz, 2H, Ar—H), 7.741(dd, 4H, J=7.9 1.4 Hz Ar—H), 7.499(t, 4H, Ar—H), 7.376 7.434 (m, 4H, Ar—H), 7.325 (td, 2H, J=7.9 1.3 Hz Ar—H), 7.250(t, 2H, Ar—H), 5.364(br, 2H, —OH).

EXAMPLE 3

[0092] Synthesis of a 3,3′-Disubstituted Chiral Phosphinite, (R)-3,3′-diphenyl-2,2′-bisdiphenylphosphinooxy-1,1′-binaphthyl (11b)

[0093] To a solution of (R)-3,3′-diphenyl-1,1′-binaphthol (876 mg, 2 mmol) in 20 ml THF at −78° C. was added n-BuLi (2.8 ml, 4.5 mmol) dropwise, the mixture was warmed to room temperature and stirred for 30 min, then cooled to −78° C., Ph2PCl (0.9 ml, 5 mmol) was added via syringe, then warmed to room temperature and stirred overnight. The THF was removed under reduced pressure, the residue was purified by basic Al2O3 (EtOAc/Hexane/Et3N=90/8/2) to give pure product (1.41 g, 87% yield).

[0094] 1 H-NMR (CD2Cl2, 360 MHz) 6.80-7.20 (m, 24H), 7.35-7.48 (m, 12H), 7.50-7.65 (m, 4H). ). 31P-NMR (CD2Cl2, 360 MHz) 112.78. ). 13C-NMR (CD2Cl2, 360 MHz) 124-150 (m). [α]D20=114.7 (c, 0.38, CHCl3). MS: 203 (100), 387 (65), 439 (48), 807 (50). HRMS C56H41O2P2 807.2566 Cal.: 807.2582.

EXAMPLE 4

[0095] General Procedure for Catalytic Asymmetric Hydrogenation of Enamides

[0096] In a glove box, the Rh-phosphine complex was made in situ by mixing Rh(COD)2PF6 (3.7 mg, 0.008 mmol) and a chiral phosphine ligand (0.8 ml of 10 mg/mL ligand in toluene, 0.012 mmol) in 19.2 ml of CH2Cl2. The mixture was stirred for 30 min. Then 2.5 ml of this solution was transferred to a 10 ml vial with an enamide substrate (0.1 mmol).

[0097] The hydrogenation was performed at room temperature under 20 psi of hydrogen pressure for 24 h. The hydrogen was released carefully and the reaction mixture was passed through a silica gel plug eluted with EtOAc. The enantiomeric excess was measured by GC or HPLC using a chiral GC or HPLC column without further purification. The absolute configuration of products was determined by comparing the sign of optical rotation with the reported data.

EXAMPLE 5

[0098] Results of Asymmetric Hydrogenation of Enamides

[0099] To examine the effectiveness of new chiral ligands, hydrogenation of a typical dehydroamino acid derivative and an enamide was carried out. The results are summarized in Table 1. The 3,3′disubstituted bisphosphinite ligands (11a-d) are more effective than BINAPO (3) for asymmetric hydrogenation.

[0100] In the similar way, the 3,3′-disubstituted bisphosphine 15 is a better ligand for Rh-catalyzed asymmetric hydrogenation than NAPHOS (6).

[0101] We conclude that introduction of 3,3′ substituted groups can restrict the rotation of phenyl groups adjacent to phosphines and therefore a well-defined chiral pocket around the transition metal is formed. The conformational rigidity is crucial for achieving high enantioselectivity for a number of asymmetric reactions.

TABLE 1
Rh(I)-catalyzed asymmetric hydrogenation
		Substrate
	Ligand	15	16
entry 1	17	73% ee	28% ee
entry 2	18	95% ee	67% ee
entry 3	19	>99% ee	94% ee
entry 4	20	95% ee	89% ee
entry 5	21	93% ee	90% ee
entry 6	22	54% ee	—
entry 7	23	99% ee	82% ee
The reaction was carried out at rt under 3 atm of H2 for 12 h in 3 ml of THF with complete conversion (S/C = 100). Ar = 3,5-Me2C6H4

EXAMPLE 6

[0102] Asymmetric Hydrogenation of Beta-Keto Esters

[0103] A number of beta-ketoesters can be reduced in high ee's using a Ru-3,3′substituted BINAPO (11d) compound as the catalysts. Particularly, the R group is aryl, hetereoaryl, substituted aryl, alkyl and substituted alkyl species. These reactions can be carried out at low pressure and low temperature, which shows advantages over the reaction carried out with Ru-BINAP complex (90 atm, 90° C.).

Asymmetric Hydrogenation
24

EXAMPLE 7

[0104] Asymmetric Synthesis of Beta-Amino Acids

[0105] Synthesis of Starting Material 3-Acetamido-3-Aryl-2-Propenoates and 3-Acetamido-3-hetero-Aryl-2-Propenoates

[0106] Typical procedure: The starting material methyl 3-acetamido-3-phenyl-2-propenoate can be conveniently synthesized from cheap acetophenone in three steps according to known literature procedure in good yields. The literatures are Zhu, G.; Zhen, Z.; Zhang, X. J. Org. Chem. 1999, 64, 6907-6910; Krapcho, A. P.; Diamanti, J. Org. Synth. 1973,5, 198-201. 1H-NMR (CDCl3, 360 MHz) δ (Z isomer) 2.17 (s, 3H), 3.77 (s, 3H), 5.29 (s, 1H), 7.37-7.45 (m, 5H); (E isomer) 2.38 (s, 3H), 3.77 (s, 3H), 6.65 (s, 1H), 7.37-7.45 (m, 5H).

[0107] An Effective New Way to Make Enam ides 25

[0108] R′, R″=alkyl, substituted alkyl aryl, substituted aryl, hetereoaryl

[0109] R=alkyl aryl

[0110] Alternatively, 3-acetamido-3-aryl-2-propenoates and 3-Acetamido-3-hetero-aryl-2-propenoates can be prepared through a new route by reacting acetamide with the corresponding beta-keto esters. A related example is demonstrated by Tschaen et al. J. Org. Chem 1995, 60, 4324. The typical procedure involves addition of the corresponding beta keto-ester, an acetamide or other amide such as enamide, Amberlyst 15 or other acid catalysts in toluene. The mixture was heated at reflux for some hours with removal of water using a Dean-Stark trap. The end product was obtained after evaporating the solvent.

[0111] Asymmetric Hydrogenation of methyl 3-acetamido-3-phenyl-2-propenoate

[0112] A dry Schlenk tube is charged with [Ru(cymene)Cl2]2 (1.53 mg, FW=612, 0.0025 mmol), chiral ligand 3,3′-diphenyl-xylyl BINAPO (11d, 4.82 mg, FW=918, 0.0053 mmol), and then is evacuated and filled with argon. DMF (must be degassed by freeze-thaw cycles) (1 ml) is introduced under stream of argon. The solution is stirred at 100° C. for 10 min under argon, giving a clear reddish brown solution. The reaction mixture is cooled and concentrated at 1 mmHg at 50° C. with vigorous stirring and then at 0.1 mmHg for 1 h to give a reddish brown solid, which is used as hydrogenation catalyst.

[0113] To a solution of above catalyst in EtOH/DCM (4 ml, 3/1) in a glove box was added substrate methyl 3-acetamido-3-phenyl-2-propenoate (109 mg, 0.5 mmol). The hydrogenation was performed at 50° C. under 78 psi of hydrogen for 15 hours (not be optimized). The bomb was then cooled to room temperature and hydrogen carefully released. The solvent was removed and the residue dissolved in ether. The ether solution was washed with water and brine and dried over sodium sulfate. The ether solution was passed through a short silica gel column and concentrated to dryness to give pure products methyl 3-acetamido-3-phenyl-2-propanoate (known compound, see: Zhu, G.; Zhen, Z.; Zhang, X. J. Org. Chem. 1999, 64, 6907-6910 (Rh/Duphos and BICP, 65% ee); Lubell, W. D.; Kitamura, M.; Noyori, R. Tetrahedron: Asymmetry 1991, 2, 543 (Ru/BINAP, poor ee)). 1H-NMR (CDCl3, 360 MHz) δ 1.92 (s, 3H), 2.76-2.83 (m, 2H), 3.53 (s, 3H), 5.34 (m, 1H), 6.65 (br, 1H), 7.18-7.27 (m, 5H). Chiral GC Condition: Chiral Select-1000 column (dimensions 15 m×0.25 mm (i.d.)). Carrier gas: He (1 ml/min), 180° C., isothermal; (S) t1=11.68 min; (R) t2=12.04 min.

Asymmetric Hydrogenation	Product	Ligand
26	27	28
29	99% ee
Ar = Ph, Py, aryl, heteroaryl, substituted aryl	98% ee	30

EXAMPLE 8

[0114] Asymmetric Allylic Alkylation

[0115] Using 3,3'disubstituted BINAPO as ligands, the Pd-catalyzed asymmetric allylic alkylation can be carried out and some results are listed below: 31

[0116] Ee values are determined by chiral HPLC (OJ Column H/IPA=95/5)

EXAMPLE 9

[0117] Asymmetric Allylic Alkylation with Nitrogen Nucleophile

[0118] Using 3,3′disubstituted BINAPO as ligands, Pd-catalyzed asymmetric allylic alkylation with nitrogen nucleophiles can be carried out and some results are listed below: 32

[0119] Ee values are determined by chiral HPLC (OJ Column H/IPA=85/15)

EXAMPLE 10

[0120] 33

[0121] Synthesis of 4-bromo-2,6-dimethoxy-phenol 17

[0122] To a 2 liter flask equipped with a magnetic stirrer, thermometer, and nitrogen inlet, was added 77 g (0.5 mol) of pyrogallol 1,3-dimethyl ether, 5.8 ml of MeOH, and 750 ml of CH2Cl2. To this solution was added 126 mg (5 mmol) of NaH (95%). The solution was stirred while cooling to −45° C. with a dry-ice acetone bath. 94 g (0.53 mol) of powdered N-bromosuccinimide was added rapidly. The reaction mixture was then stirred for 1 hour at −35° C., heated to room temperature over next 30 min, and finally refluxed for 30 min. The CH2Cl2 was removed under reduced pressure and the residue solidified. The tan solid was broken up and stirred well with 1 liter of ether. This was filtered and the residue was washed well with ether. The ether was evaporated under reduced pressure to yield a tan solid. The solid was placed in a 5 liter flask with 3 liters of ligroin (bp: 90-110° C.) and heated with stirring to 80° C. The hot solution was decanted from the brown oil and the hot yellow solution was allowed to cool at room temperature for 3 hr. The white needles was filtered off and dried to yield 74 g (63%) of 17.

[0123] Ref. J. Org. Chem. Vol. 50, 1985, 1099.

[0124] Synthesis of 3,4,5-trimethoxybromobenzene 18

[0125] A mixture of 74 g (0.32 mol) of 4-bromo-2,6-dimethoxy-phenol 17 and 32 g (0.8 mol) of NaOH in 850 ml of H2O was cooled to 10° C. and 45 ml (0.48 mmol) of dimethyl sulfate was added. The mixture was refluxed for 3 h and an equal amount of dimethyl sulfate (total 0.96 mol) was then added. The mixture was refluxed for another 3 h. Upon cooling overnight, the gray product solidified and was filtered off and dissolved in 1.2 l of ether. The ether solution was filtered to remove insoluble impurity and washed sequentially with 5% NaOH solution (200 ml), water (2×200 mL), and brine (200 mL). The ether phase was dried over Na2SO4 to give a off-white solid, which was recrystallized in hexane (300 ml) to give 62.3 g (79%) of 18.

[0126] Synthesis of (3,4,5-trimethoxyphenyl)diphenylphosphine 19

[0127] To a solution of 3,4,5-trimethoxybromobenzene 18 (62.3 g, 0.25 mol) in dry THF (200 ml) was added BuLi solution (169 ml, 1.6M in hexane, 0.27 mol) dropwise at −78° C. within 45 min. The resulting beige-colored suspension was stirred for an additional 1 h at −78° C. Then PPh2Cl (61 g, 0.277 mol, 49.7 ml) was added dropwise. The addition was complete within 2 h. The resulting yellow solution was allowed to warm to 0° C. within 2 h and quenched by addition of NH4Cl solution (200 ml). The organic layer was separated, washed with brine (250 ml), dried (Na2SO4), filtered, and evaporated. The solid was recrystallized from methanol to give 69.5 g(80%) of 19.

[0128] Ref.: Helvetica ChimicaActa Vol. 74, 1991, 370-389

[0129] Synthesis of 3,4,5-trimethoxyphenyl)diphenylphosphine oxide 20

[0130] To a suspension of 19 (69.5 g, 0.2 mmol) in MeOH (500 ml) was added dropwise 30% H2O2 (24.5 g, 0.215 mol) at 0° C. The resulting clear solution was stirred at ambient temperature for 1 h. Then it was treated with sat. Na2SO3 solution (75 ml) and IN HCl solution (50 ml). The mixture was concentrated under reduced pressure to remove the MeOH. The solid residue was dissolved in CH2Cl2 (300 ml), washed with water (2×200 ml) and brine (200 ml), dried over Na2SO4, and evaporated. To the resulting white solid was added 300 ml hexane and the resulting suspension was stirred vigorously at room temperature. Filtration of the white solid powder gave 67.2 g (0.182 mol, 91%) of pure 20.

[0131] Ref: Helvetica Chimica Acta Vol. 74, 1991, 370-389

[0132] Synthesis of (2-iodo-3,4,5-trimethoxyphenyl)diphenylphosphine oxide 21

[0133] To a solution of (i-Pr)2NH (31.88 ml, 23.02 g, 0.227 mol) in dry THF (200 ml)was added n-BuLi solution (125 ml, 1.6M in hexane, 0.2 mol) dropwise at −78° C. The addition was complete within 15 min. After stirred at 0° C. for 10 min, the LDA solution was re-cooled to −78° C. It was then added via cannula to a flask containing a solution of 20 (67.2 g, 0.182 mol) in dry THF (200 ml) over 20 min. During the addition, the mixture was turned reddish-brown, and eventually a beige suspension was formed. After the reaction mixture was stirred for an additional 15 min at −78° C., a solution of 12 (50.6 g, 0.2 mol) in THF (200 ml) was added dropwise. The addition was complete in 3 h. A reddish-brown viscous paste was formed at the end of the addition. Then, the cooling bath was removed, and the mixture was allowed to warm to 0° C. to form a clear red solution. The mixture was quenched by the addition of a Na2S2O3 solution (12 g in 100 ml H2O). The solution was concentrated to remove THF. The residue was dissolved in 300 ml of CH2Cl2, washed with water (2×200 ml) and brine (200 ml), dried over Na2SO4, and evaporated. The brown paste was recrystallized in EtOAc (100 ml) to give 55 g (62%) of 21.

[0134] Ref: Helvetica Chimica Acta Vol. 74, 1991, 370-389

[0135] Synthesis of (2-phenyl-3,4,5-trimethoxyphenyl)diphenylphosphine oxide 22

[0136] To a 2 liter Schlenk flask was added (2-iodo-3,4,5-trimethoxyphenyl) diphenylphosphine oxide 21 (30 g, 61 mmol), phenylboronic acid (11.1 g, 91 mmol), and degassed THF (800 ml). A solution of degassed saturated K2CO3 (400 ml) was added afterwards. The whole mixture was degassed with nitrogen for an additional 10 min. Then, Pd(PPh3)4 (1.22 mmol, 1.4 g) was added in the solution through one portion. The mixture was stirred at reflux under nitrogen for 24 hrs. In situ 31PNMR showed that the reaction was complete. The reaction mixture was concentrated under reduced pressure to remove THF and 400 ml of CH2Cl2 was then added. The CH2Cl2 layer was washed with water (200 ml) and brine (200 ml), dried over Na2SO4, and evaporated. The solid residue was recrystallized from EtOAc (100 ml) to give off-white product 22 (23 g). The mother liquid was passed through a silica gel column to give another 4 g of product 22. The total yield was 98%.

[0137] Synthesis of (2-iodo-6-phenyl-3,4,5-trimethoxyphenyl)diphenylphosphine oxide 23

[0138] To a solution of (2-phenyl-3,4,5-trimethoxyphenyl)diphenylphosphine oxide 22 (26.5 g, 59.7 mmol) in dry THF (500 ml) was added t-BuLi (47.7 ml, 1.5M in pentane, 71.6 mmol) dropwise at −90° C. The addition was complete within 2 hrs. The solution was allowed to warm to −78° C. and stirred for an additional 3 h. Then a solution of 12 in THF (100 ml) was added dropwise at this temperature. The addition was complete in 2 h. The resulting dark solution was allowed to warm to room temperature and stirred overnight. A solution of Na2S2O3 (12 g in 100 ml H2O) was added. The resulting yellow solution was concentrated under reduced pressure. To the residue was added 500 ml of CH2Cl2. The CH2Cl2 layer was washed with water (100 ml) and brine (100 ml), dried over Na2SO4, and evaporated. The residue was recrystallized from EtOAc (100 ml) to give a pure brown solid 23 (24 g). The mother liquid was passed through a silica gel column to give another 5 g of product. The total yield is 85%.

[0139] Synthesis of (RS)-(3,3′-diphenyl-4,4′,5,5′,6,6′-hexamethoxybiphenyl-2,2′-diyl)bis(diphenylphosphine oxide) 24

[0140] A mixture of (2-iodo-6-phenyl-3,4,5-trimethoxyphenyl)diphenylphosphine oxide 23 (7.4 g, 12.6 mmol), Cu powder (252 mmol, 16 g, activated by I2 treatment), and DMF (200 ml) was stirred at 155° C. for 1 hr. The cold mixture was evaporated to dryness at the rotor evaporator at 70° C. The residue was treated for a few min with CH2Cl2 (200 ml). The solid was removed by filtration and washed with CH2Cl2 (200 ml). The combined filtrate was washed with sat. NH4Cl solution (2×100 mL), dried over Na2SO4, and evaporated. The residue was crystallized from EtOAc (100 ml) to give 5 g (90%) of white product 24.

[0141] Resolution of (3,3′-diphenyl-4,4′,5,5′,6,6′-hexamethoxybiphenyl-2,2′-diyl)bis(diphenylphosphine oxide) 25

[0142] To a mixture of (RS)-(3,3′-diphenyl-4,4′,5,5′,6,6′-hexamethoxybiphenyl-2,2′-diyl)bis(diphenylphosphine oxide) 24 (2.3 g, 2.5 mmol) and (−)-DTTA (−0.966 g, 2.5 mmol) was added 40 ml of i-PrOH. The resulting slurry was heated to reflux to get a clear solution. Then it was cooled slowly to room temperature and stirred overnight. The salt of (−)-25 and (−)-DTTA was obtained as white powder through filtration(ee: 95%). The salt was recrystallized one more time from 25 ml i-PrOH and 1.1 g of solid was obtained. The solid was dissolved in 50 ml of CH2Cl2, washed with 3N NaOH (2×50 ml) and water (3×50 mL), dried over Na2SO4, and evaporated. The solid (97.7%, 0.86 g) was recrystallized from acetone to give enantiomerically pure product 25 (0.69 g, 60%, ee>99.5%). Synthesis of (−)-(3,3′-diphenyl-4,4′,5,5′,6,6′-hexamethoxybiphenyl-2,2′-diyl)bis(diphenylphosphine) 26.

[0143] To a solution of (−)-(3,3′-diphenyl-4,4′,5,5′,6,6′-hexamethoxybiphenyl-2,2′-diyl)bis(diphenylphosphine oxide) 25 (700 mg, 0.79 mmol, resolved from (−)-DTTA), tributylamine (6.5 ml, 27.3 mmol), and xylene (100 ml) was added HSiCl3 (1.72 ml, 17 mmol) dropwise at 0° C. The reaction was stirred at reflux for 2 days. Some precipitates came out during the course. After cooled down, the reaction mixture was quenched with 30% degassed NaOH solution (20 ml) in an ice-water bath. The resulting solution was kept at 60° C. for 1 h. The organic phase was transferred into another Schlenk flask through cannula. The water phase was re-washed with CH2Cl2 (30 ml*2). The combined organic phase was washed with water (50 ml), dried over Na2SO4, and evaporated under reduced pressure. The resulting yellow residue was dissolved in CH2Cl2 (10 ml) and passed through a basic Al2O3 column to give a pure white solid 26 (400 mg, 59%).

EXAMPLE 11

[0144] 34

[0145] (2,5-Dimethoxyphenyl)diphenylphosphine Oxide

[0146] At −78° C., 2.5M n-BuLi in hexane (48 mL, 0.12 mol) was slowly added to a solution of 1-Bromo-2,5-dimethoxybenzene (27, 25 g, 0.115 mol) in THF (250 mL) causing the solution to become dark yellow (solid suspension). The reaction mixture was stir at this temp for about 30 minutes, following by addition of diphenylchlorophosphine (21.5 ml, 0.12 mol). During the addition, control the temp below −50° C. (add slowly). The resulting yellow solution was allowed to warm up to room temp (take about two hours). The saturated NH4Cl solution (200 ml) was added and reaction mixture form two layers. The organic layer was washed with brine (2×100 mL) and dried (Na2SO4). The solvent was removed under vacuum to give a white solid.

[0147] Add MeOH (200 mL) to the resulting white solid to form suspension. At 0° C., 33% H2O2 (14 ml, 0.13 mol) was slowly added to above MeOH suspension. The addition process takes about 20 minutes and the solid vanished promptly after all H2O2 was added. The mixture was allowed to stir for one hour at 0° C., follow by adding saturated NaHSO3 solution (15 ml) and stir for 30 minutes (the KI-Starch paper was applied here to make sure all peroxide was reduced). The solvent was removed under vacuum to give a white solid. The resulting solid was dissolved in CH2Cl2 (200 mL) and was washed with water (150 mL) and brine (150 mL), dried (Na2SO4). The solvent was also removed under vacuum to give a white solid. The crude product was treated with hot hexane (2×100 mL) (to remove trace amount of impurity) to give pure product (28, 37.3 g, 95.8%).

[0148] (3,6-Dimethoxy-2-iodophenyl)diphenylphosphine Oxide

[0149] A solution of LDA (6 mmol) 1.5M in pentane was slowly added to the phosphine oxide (28, 1.69 g, 5 mmol) in THF (60 mL) at 100° C. The resulting dark yellow solution (solid suspension) was allowed to warm up to −78° C. (take 30 minutes) and then stirred 3.5 hours at this temp. during which time the white solid precipitated. Solid I2 (1.78 g, 7 mmol) was added against a counter flow of N2 to the anion in THF at −78° C. The reaction was allowed to come to 0° C. and quenched with Na2S2O3 aq. solution (10 mL). The solvent was removed under vacuum and the residue was extracted with CH2Cl2 (50 mL), washed with water (50 mL), brine (50 ml) and dried (Na2SO4). The solvent was removed and the brown oil residue was treated with EtOAc (10 mL) (to wash out most of the color impurities, the product form white solid in EtOAc). Then the vacuum filtration gives the white solid (29, 1.0 g, 43%)

[0150] 2,2′-(Diphenylphosphinoyl)3,3′,6,6′-tetramethoxybiphenyl

[0151] Copper powder (320 mg, 5 mmol) was added to a solution of the iodide (29, 116 mg, 0.25 mmol) in DMF (10 mL) and the reaction mixture heated to reflux for 8 hours. During the reflux, white solid formed along the wall of flask. The mixture was treated under vacuum to remove most of the solvent (before it cooled). The residue was extracted with CH2Cl2 (20 mL) and washed with water (2×10 mL), brine (10 mL) and dried (Na2SO4). The solvent was removed under vacuum and the resulting solid was washed with EtOAc (2 mL) to give a white solid (30, 70 mg, 83%).

[0152] Resolution of 2,2′-(diphenylphosphinoyl)3,3′,6,6′-tetramethoxybiphenyl

[0153] (−) DTTA (0.579 g, 1.5 mmol) was added to diphosphine oxide (30, 0.674 g, 1 mmol) in EtOH (29 mL) solution(at this time, DTTA can not dissolve in EtOH solution). The reaction mixture was heated up to reflux until all solid suspension was completely dissolved (take about 20 minutes). The resulting solution was allowed to stir overnight until crystal formed. The mixture was filtrated under vacuum and washed with cold EtOH (5 mL). The resulting solid (0.405 g, 75.1%) was added to CH2Cl2 (20 mL) and NaOH (20 mL, 10% aq.) solution for about 5 minutes, and the entire insoluble solid disappeared. The organic layer was washed with water (2×10 mL), brine (10 mL) and dried (Na2SO4). The solvent was removed under vacuum to give a white solid (31, 99.3% ee).

[0154] 2,2′-Diphenylphosphanyl-3,6,3′,6′-tetramethoxybiphenyl

[0155] HSiCl3 (542 mg, 0.4 mL) and NBu3 (1.48 g, 1.9 mL) were added to diphosphine oxide (31, 70 mg, 0.1 mmol) in xylene (5 mL) solution under N2 atmosphere. The reaction mixture was heated to reflux for 3 hours. The mixture was allowed to cool down to room temp. Then the degassed NaOH aq. solution (10%, 5 mL) was added to reaction mixture at 0° C. and stir for one hour. The organic layer was washed with degassed water (2×10 mL), NH4Cl aq. solution (10 mL), brine (10 mL) and dried (Na2SO4). The solvent was removed under vacuum to give a pale yellow solid. After a short plug (silica gel, elute with CH2Cl2:Hexane=1:1), the solvent was evaporated under vacuum to give a white solid (still not pure white, a little bit pale yellow color) (32, 50 mg, 75%).

EXAMPLE 12

[0156] Asymmetric Hydrogenation of Enamides Facilitated by Rh-Complexes with (−) (3,3′-diphenyl-4,4′,5,5′, 6,6′-hexamethoxybiphenyl-2,2′-diyl)bis-(diphenylphosphine) (26)

[0157] Rh-complexes with (−) (3,3′-diphenyl-4,4′,5,5′, 6,6′-hexamethoxybiphenyl-2,2′-diyl)bis(diphenylphosphine) (26) are good catalysts for hydrogenation of enamides. Introduction of 3,3′ substituted groups have some effects on enantioselectivity of asymmetric hydrogenation of enamides. Cyclic enamides can be hydrogenated with good enantioselectivity. 35

[0158] The present invention has been described with particular reference to the preferred embodiments. It should be understood that the foregoing descriptions and examples are only illustrative of the invention. Various alternatives and modifications thereof can be devised by those skilled in the art without departing from the spirit and scope of the present invention. Accordingly, the present invention is intended to embrace all such alternatives, modifications, and variations that fall within the scope of the appended claims.

Claims

1. A ligand represented by the formula or its enantiomer:

2. The ligand of claim 1, wherein said substituted alkyl has one or more substituents, each independently selected from the group consisting of: halogen, ester, ketone, carboxylic acid, hydroxy, alkoxy, aryloxy, thiol, alkylthio and dialkylamino.

3. The ligand of claim 1, wherein said alkylene is selected from the group consisting of compounds represented by the formula: —(CH2)n—, wherein n is an integer in the range of from 1 to 8.

4. The ligand of claim 1, wherein each of said aryl groups optionally has one or more substituents, each independently selected from the group consisting of: halogen, ester, ketone, sulfonate, phosphonate, hydroxy, alkoxy, aryloxy, thiol, alkylthiol, nitro, amino, vinyl, substituted vinyl, carboxylic acid, sulfonic acid and phosphine.

5. The ligand of claim 1, wherein each of said arylene groups optionally has one or more substituents, each independently selected from the group consisting of: halogen, ester, ketone, sulfonate, phosphonate, hydroxy, alkoxy, aryloxy, thiol, alkylthiol, nitro, amino, vinyl, substituted vinyl, carboxylic acid, sulfonic acid and phosphine.

6. The ligand of claim 1, wherein each of said arylene groups is independently selected from the group consisting of: 1,2-divalent phenyl, 2,2′-divalent-1,1′-biphenyl, 2,2′-divalent-1,1′-binaphthyl and ferrocene.

7. The ligand of claim 1, wherein said ligand is a racemic mixture of enantiomers.

8. The ligand of claim 1, wherein said ligand is a non-racemic mixture of enantiomers.

9. The ligand of claim 1, wherein said ligand is one of the enantiomers.

10. The ligand of claim 1, having an optical purity of at least 85% ee.

12. The ligand of claim 1, having an optical purity of at least 95% ee.

13. The ligand of claim 1, wherein said ligand is s elected from the group consisting of compounds represented by the following formulas:

14. The ligand of claim 1, wherein said ligand is selected from the group consisting of compounds represented by the following formulas:

15. The ligand of claim 1, wherein said ligand is selected from the group consisting of compounds represented by the formulas:

16. The ligand of claim 1, represented by the formula: or

17. The ligand of claim 1, represented by the formula:

18. The ligand of claim 1, represented by the formula:

19. A catalyst prepared by a process comprising: contacting a transition metal salt, or a complex thereof, and a ligand selected from the group consisting of compounds represented by the formula or its enantiomer: 43wherein each X and X′ is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2; wherein each Z and Z1 is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2; or wherein Z and Z1 together form the bridging group A-B-A1; wherein each Z′, Z″, Z1′ and Z1″ is independently selected from the group consisting of: H, alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2, or wherein Z′ and Z together form the bridging group A′-B-A; Z′ and Z together form a fused cycloaliphatic or aromatic group; Z1 and Z1′ together form the bridging group A1-B1-A1′; and/or Z1 and Z1′ together form a fused cycloaliphatic or aromatic group; wherein each A, A′, A1 and A1′ is independently selected from the group consisting of: O, CH2, NH, NR, S, CO and a bond; wherein each B and B1 is independently selected from the group consisting of: linear, branched or cyclic alkylene of 1 to 6 carbon atoms, arylene of 6 to 12 carbon atoms, O, CH2, NH, NR, S, CO, SO2, P(O)R, P(O)OR, POR, SiR2 and a bond; wherein each T is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, substituted aryl, alkoxide, aryloxide, R, R′, R″, YR′, YR″, Y′R′ and Y″R″; or wherein two T groups together form an alkylene, arylene, alkylenediamino, arylenediamino, alkelenedioxyl or arylenedioxyl; wherein each T′ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, substituted aryl, alkoxide, aryloxide, R, R′, R″, YR′, YR″, Y′R′ and Y″R″; or wherein two T′ groups together form an alkylene, arylene, alkylenediamino, arylenediamino, alkelenedioxyl or arylenedioxyl; wherein each R, R′ and R″ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, aralkyl and alkaryl of 1 to 22 carbon atoms; or wherein two R groups, two R′ groups or two R″ group together form an alkylene or arelene group; and wherein each Y, Y′ and Y″ is independently selected from the group consisting of: O, CH2, NH, S and a bond between carbon and phosphorus; with the proviso that when the Y group at the 2′ position is a bond between carbon and phosphorus, X′ is hydrogen.

20. The catalyst of claim 19, wherein said substituted alkyl has one or more substituents, each independently selected from the group consisting of: halogen, ester, ketone, carboxylic acid, hydroxy, alkoxy, aryloxy, thiol, alkylthio and dialkylamino.

21. The catalyst of claim 19, wherein said alkylene is selected from the group consisting of compounds represented by the formula: —(CH2)n—, where n is an integer in the range of from 1 to 8.

22. The catalyst of claim 19, wherein each of said aryl groups optionally has one or more substituents, each independently selected from the group consisting of: halogen, ester, ketone, sulfonate, phosphonate, hydroxy, alkoxy, aryloxy, thiol, alkylthiol, nitro, amino, vinyl, substituted vinyl, carboxylic acid, sulfonic acid and phosphine.

23. The catalyst of claim 19, wherein each of said arylene groups optionally has one or more substituents, each independently selected from the group consisting of: halogen, ester, ketone, sulfonate, phosphonate, hydroxy, alkoxy, aryloxy, thiol, alkylthiol, nitro, amino, vinyl, substituted vinyl, carboxylic acid, sulfonic acid and phosphine.

24. The catalyst of claim 19, wherein each of said arylene groups is independently selected from the group consisting of: 1,2-divalent phenyl, 2,2′-divalent-1,1′-biphenyl, 2,2′-divalent-1,1′-binaphthyl and ferrocene.

25. The catalyst of claim 19, wherein said ligand is a racemic mixture of enantiomers.

26. The catalyst of claim 19, wherein said ligand is a non-racemic mixture of enantiomers.

27. The catalyst of claim 19, wherein said ligand is one of the enantiomers.

28. The catalyst of claim 19, having an optical purity of at least 85% ee.

29. The catalyst of claim 19, having an optical purity of at least 95% ee.

30. The catalyst of claim 19, wherein said transition metal is selected from the group consisting of: Ag, Pt, Pd, Rh, Ru, Ir, Cu, Ni, Mo, Ti, V, Re and Mn.

31. The catalyst of claim 19, wherein said transition metal is selected from the group consisting of: Pt, Pd, Rh and Ru.

32. The catalyst of claim 19, wherein said transition metal salt, or complex thereof, is selected from the group consisting of: AgX; Ag(OTf); Ag(OTf)2; AgOAc; PtCl2; H2PtCl4; Pd2(DBA)3; Pd(OAc)2; PdCl2(RCN)2; (Pd(allyl)Cl)2; Pd(PR3)4; (Rh(NBD)2)X; (Rh (NBD)Cl)2; (Rh(COD)Cl)2; (Rh(COD)2)X; Rh(acac)(CO)2; Rh(ethylene)2(acac); (Rh(ethylene)2Cl)2; RhCl(PPh3)3; Rh(CO)2Cl2; RuHX(L)2(diphosphine), RuX2(L)2 (diphosphine), Ru(arene)X2(diphosphine), Ru(aryl group)X2; Ru(RCOO)2(diphosphine); Ru(methallyl)2(diphosphine); Ru(aryl group)X2(PPh3)3; Ru(COD)(COT); Ru(COD)(COT)X; RuX2(cymen); Ru(COD)n; Ru(aryl group)X2(diphosphine); RuCl2(COD); (Ru(COD)2)X; RuX2(diphosphine); RuCl2(═CHR)(PR′3)2; Ru(ArH)Cl2; Ru(COD)(methallyl)2; (Ir(NBD)2Cl)2; (Ir(NBD)2)X; (Ir(COD)2Cl)2; (Ir(COD)2)X; CuX (NCCH3)4; Cu(OTf); Cu(OTf)2; Cu(Ar)X; CuX; Ni(acac)2; NiX2; (Ni(allyl)X)2; Ni(COD)2; MoO2(acac)2; Ti(OiPr)4; VO(acac)2; MeReO3; MnX2 and Mn(acac)2; wherein each R and R′ is independently selected from the group consisting of: alkyl or aryl; Ar is an aryl group; and X is a counteranion.

33. The catalyst of claim 32, wherein L is a solvent molecule and wherein said counteranion X is selected from the group consisting of: halogen, BF4, B(Ar)4, wherein Ar is fluorophenyl or 3,5-di-trifluoromethyl-1-phenyl, ClO4, SbF6, PF6, CF3SO3, RCOO and a mixture thereof.

34. The catalyst of claim 19, prepared in situ or as an isolated compound.

35. The catalyst of claim 19, wherein said transition metal salt, or a complex thereof is selected from the group consisting of: [Rh(COD)Cl]2, [Rh(COD)2]X, [Ir(COD)Cl]2, [Ir(COD)2]X, Rh(acac)(CO)2, Ni(allyl)X, Pd2(dba)3, [Pd(allyl)Cl]2, Ru(RCOO)2(diphosphine), RuX2(diphosphine), Ru(methylallyl)2(diphosphine) and Ru(aryl)X2(diphosphine), wherein X is selected from the group consisting of: BF4, ClO4, SbF6, CF3SO3, Cl and Br; and wherein said ligand is selected from the group consisting of compounds represented by the formula:

36. A process for preparation of an asymmetric compound comprising: contacting a substrate capable of forming an asymmetric product by an asymmetric reaction and a catalyst prepared by a process comprising: contacting a transition metal salt, or a complex thereof, and a ligand selected from the group consisting of compounds represented by the formula or its enantiomer: 46wherein each X and X′ is independently selected from the group consisting of. alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2; wherein each Z and Z1 is independently selected from the group consisting of: alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2; or wherein Z and Z1 together form the bridging group A-B-A1; wherein each Z′, Z″, Z1′ and Z1″ is independently selected from the group consisting of: H, alkyl, aryl, substituted alkyl, substituted aryl, OR, SR, NR2, COOR, halide, SiR3, P(O)R2, P(O)(OR)2 and P(OR)2, or wherein Z′ and Z together form the bridging group A′-B-A; Z′ and Z together form a fused cycloaliphatic or aromatic group; Z1 and Z1′ together form the bridging group A1-B1-A1′; and/or Z1 and Z1′ together form a fused cycloaliphatic or aromatic group; wherein each A, A′, A1 and A1′ is independently selected from the group consisting of: O, CH2, NH, NR, S, CO and a bond; wherein each B and B1 is independently selected from the group consisting of: linear, branched or cyclic alkylene of 1 to 6 carbon atoms, arylene of 6 to 12 carbon atoms, O, CH2, NH, NR, S, CO, SO2, P(O)R, P(O)OR, POR, SiR2 and a bond; wherein each T is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, substituted aryl, alkoxide, aryloxide, R, R′, R″, YR′, YR″, Y′R′ and Y″R″; or wherein two T groups together form an alkylene, arylene, alkylenediamino, arylenediamino, alkelenedioxyl or arylenedioxyl; wherein each T′ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, substituted aryl, alkoxide, aryloxide, R, R′, R″, YR′, YR″, Y′R′ and Y″R″; or wherein two T′ groups together form an alkylene, arylene, alkylenediamino, arylenediamino, alkelenedioxyl or arylenedioxyl; wherein each R, R′ and R″ is independently selected from the group consisting of: alkyl, substituted alkyl, aryl, aralkyl and alkaryl of 1 to 22 carbon atoms; or wherein two R groups, two R′ groups or two R″ group together form an alkylene or arelene group; and wherein each Y, Y′ and Y″ is independently selected from the group consisting of: O, CH2, NH, S and a bond between carbon and phosphorus; with the proviso that when the Y group at the 2′ position is a bond between carbon and phosphorus, X′ is hydrogen.

37. The process of claim 36, wherein said asymmetric reaction is selected from the group consisting of: hydrogenation, hydride transfer, allylic alkylation, hydrosilylation, hydroboration, hydrovinylation, hydroformylation, olefin metathesis, hydrocarboxylation, isomerization, cyclopropanation, Diels-Alder reaction, Heck reaction, isomerization, Aldol reaction, Michael addition, epoxidation, kinetic resolution and [m+n] cycloaddition wherein m=3 to 6 and n=2.

38. The process of claim 37, wherein said transition metal is selected from the group consisting of: Ag, Pt, Pd. Rh, Ru, Ir, Cu, Ni, Mo, Ti, V, Re and Mn.

39. The process of claim 37, wherein said asymmetric reaction is hydrogenation and said substrate is selected from the group consisting of imine, ketone, ethylenically unsaturated compound, enamine, enamide and vinyl ester.

40. The process of claim 37, wherein said asymmetric reaction is a silver-catalyzed asymmetric [3+2] cycloaddition of an azomethine ylide with a dipolarophile.

41. The process of claim 37, wherein said asymmetric reaction is a palladium-catalyzed allylic alkylation and said substrate is an allylic ester.

42. The process of claim 37, wherein said asymmetric palladium-catalyzed allylic alkylation reaction is a kinetic resolution reaction and said substrate is a racemic allylic ester.

43. The process of claim 37, wherein said asymmetric reaction is hydrogenation, said substrate is a beta-ketoester, said transition metal is Ru and said asymmetric compound is a beta-hydroxyester.

44. The process of claim 37, wherein said asymmetric reaction is hydrogenation, said substrate is an enamide, said transition metal is Ru and said asymmetric compound is a beta amino acid.

45. The process of claim 37, wherein said ligand is selected from the group consisting of compounds represented by the formula:

46. The process of claim 45, wherein said asymmetric reaction is hydrogenation, said substrate is a beta-ketoester, said transition metal is Ru and said asymmetric compound is a beta-hydroxyester.

47. The process of claim 45, wherein said asymmetric reaction is hydrogenation, said substrate is an enamide, said transition metal is Ru and said asymmetric compound is a beta amino acid.