Catalytic reactions performed with catalysts classified in B01J31/00

BPERFORMING OPERATIONS TRANSPORTING B01Physical, chemical processing B01JCHEMICAL OR PHYSICAL PROCESSES

B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00

B01J2231/005General concepts B01J2231/10Polymerisation reactions involving at least dual use catalysts B01J2231/12Olefin polymerisation or copolymerisation B01J2231/122Cationic (co)polymerisation B01J2231/125Radical (co)polymerisation B01J2231/127Anionic (co)polymerisation B01J2231/14Other (co) polymerisation B01J2231/20Olefin oligomerisation or telomerisation B01J2231/30Addition reactions at carbon centres B01J2231/32Addition reactions to C=C or C-C triple bonds B01J2231/321Hydroformylation, metalformylation, carbonylation or hydroaminomethylation B01J2231/322Hydrocyanation B01J2231/323Hydrometalation B01J2231/324Cyclisations via conversion of C-C multiple to single or less multiple bonds B01J2231/325Cyclopropanations B01J2231/326Diels-Alder or other [4+2] cycloadditions B01J2231/327Dipolar cycloadditions B01J2231/328Cycloadditions involving more than 2 components or moieties B01J2231/34Other additions B01J2231/3411,2-additions B01J2231/342Aldol type reactions B01J2231/343to prepare cyanhydrines B01J2231/344Boronation B01J2231/345with organometallic complexes B01J2231/346Mannich type reactions B01J2231/347via cationic intermediates B01J2231/3481,4-additions B01J2231/3491,2- or 1,4-additions in combination with further or prior reactions by the same catalyst, i.e. tandem or domino reactions B01J2231/40Substitution reactions at carbon centres, e.g. C-C or C-X B01J2231/42Catalytic cross-coupling B01J2231/4205C-C cross-coupling B01J2231/4211Suzuki-type B01J2231/4216with R= alkyl B01J2231/4222with R'= alkyl B01J2231/4227with Y= Cl B01J2231/4233Kumada-type B01J2231/4238Negishi-type B01J2231/4244with R= alkyl B01J2231/425with R'= alkyl B01J2231/4255Stille-type B01J2231/4261Heck-type B01J2231/4266Sonogashira-type B01J2231/4272via enolates or aza-analogues, added as such or made in-situ B01J2231/4277C-X Cross-coupling B01J2231/4283using N nucleophiles B01J2231/4288using O nucleophiles B01J2231/4294using S nucleophiles B01J2231/44Allylic alkylation, amination, alkoxylation or analogues B01J2231/46C-H or C-C activation B01J2231/48Ring-opening reactions B01J2231/482asymmetric reactions B01J2231/485kinetic resolution of epoxide racemates B01J2231/487by hydrolysis B01J2231/49Esterification or transesterification B01J2231/50Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds B01J2231/52Isomerisation reactions B01J2231/54Metathesis reactions B01J2231/543alkene metathesis B01J2231/546alkyne metathesis B01J2231/60Reduction reactions B01J2231/62Reductions in general of inorganic substrates B01J2231/625of CO2 B01J2231/64Reductions in general of organic substrates B01J2231/641Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations B01J2231/643of R2C=O or R2C=NR (R= C, H) B01J2231/645of C=C or C-C triple bonds B01J2231/646of aromatic or heteroaromatic rings B01J2231/648Fischer-Tropsch-type reactions B01J2231/70Oxidation reactions B01J2231/72Epoxidation B01J2231/74Aziridination B01J2231/76Dehydrogenation B01J2231/763mof -CH-XH (X= O, NH/N, S) to -C=X or -C-X triple bond species B01J2231/766of -CH-CH- or -C=C- to -C=C- or -C-C- triple bond species