Black et al, Tetrahedron, 1995, “Synthesis of indolo[3,2-b]carbazoles from . . . ”, 51(43):11801-8.* |
Biswas et al., 1998, CAS:130:110177.* |
Swindells et al., 1956, CAS:51:1737.* |
Liu et al., 1994, “Indollo[3,2-b]carbazole:a dietary-derived factor that exhibit both antiestrogenic ..”, 86(23): 1758-65.* |
Aygün et al. (2003), “Synthesis and Biological Evaluation of Structural Variants of Carbazoquinocin C,” Journal of Heterocyclic Chemistry 40(3):411-417. |
Black et al. (1993), “Calix[3]indoles, New Macrocyclic Tris(indolylmethylene) Compounds with 2,7-Linkages,” J. Chem. Soc., Chem. Commun., 10:819-821. |
Black et al. (1995), “Synthesis of Indolo[3,2-b]carbazoles from 4,6-Dimethoxyindole and Aryl Aldehydes,” Tetrahedron 51(43): 11801-11808. |
Hino et al. (1973), “Preparation of 3-Substituted 2-Indolinethiones via Diindolyl Disulfides. Reaction of 3-Substituted Indoles with Sulfur Monochloride,” Chemical & Pharmaceutical Bulletin 21(12):2739-2748 (abstract only). |
Hino et al. (1974), “Reaction of Skatole with Iodine in the Presen ce of Thiourea,” Chemical & Pharmaceutical Bulletin 22(11):2728-2731 (abstract only). |
Hünig et al. (1976), “Synthese Vinyloger und Azavinyloger Redoxsysteme Mit Indolylresten Als Endgruppen, ” Liebigs Ann. Chem. 6:1039-1059. |
Jackson et al. (1987), “Electrophilic Substitution in Indoles. Part 15. The Reaction Between Methylenedi-indoles and p-Nitrobenzenediazonium Fluorobate,” J. Chem. Soc. Perkin Trans. I 11:2543-2551. |
Lau et al. (1986), “Reductive Deoxygenation of Aryl Aldehydes and Ketones and Benzylic, Allylic, and Tertiary Alcohols by ZnI2-NaCNBH3,” J. Org. Chem. 51(15):3038-3043. |
Napolitano et al. (1993), “Oxidation Chemistry of 5,6-Dihydroxy-2-methylindole,” Tetrahedron 49(40):9143-9150. |
Pindur et al. (1987), “Reaktivität und Reaktionswege von Methylsubstituierten Bisindolylcarbenium-Ionen,” Journal of Heterocyclic Chemistry 24(1):159-163. |
Von Dobeneck et al. (1969), “α.β′-Diindolymethane und -Methene. Der Urorosein-Chromophor,” Chemishe Berichte. 102(4):1347-1356. |
Wille et al. (2001), “Malassezin-A Novel Agonist of the Arylhydrocarbon Receptor from the Yeast Malassezia furfur,” Bioorganic & Medicinal Chemistry 9:955-960. |
Bonnesen et al. (2001), “Dietary Indoles and Isothiocyanates That Are Generated from Cruciferous Vegetables Can Both Stimulate Apoptosis and Confer Protection Against DNA Damage in Human Colon Cell Lines,” Cancer Research 61: 6120-6130. |
Bradlow et al. (1991), “Effects of Dietary Indole-3-carbinol on Estradiol Metabolism and Spontaneous Mammary Tumors in Mice,” Carcinogenesis 12(9):1571-1574. |
Chinni et al. (2001), “Indole-3-carbinol (I3C) Induced Cell Growth Inhibition, G1 Cell Cycle Arrest and Apoptosis in Prostate Cancer Cells,” Oncogene 20:2927-2936. |
Grotta et al. (1961), “Preparation of Some Condensed Ring Carbazole Derivatives,” J. Org. Chem. 26:1509-1511. |
Kistenmacher et al. (1992), “A Direct Synthesis of Indolocarbazoles via New Dinitroterphenyl Precursors,” J. Heterocyclic Chem. 29:1237-1239. |
Knölker et al. (1998), “Iron-Mediated Synthesis of Indolo[2,3-b]carbazole,” Tetrahedron Letters 394007-4008. |
Knölker et al. (2000), “Transition Metal Complexes in Organic Synthesis. Part 61: Convergent Synthesis of Indolo[2,3-b]carbazole by an Iron-Mediated Bidirectional Annulation of Two Indole Rings,” Tetrahedron 56:4733-4737. |
Kojima et al. (1994), “Chemoprevention of Spontaneous Endometrial Cancer in Female Donryu Rats by Dietary Indole-3-carbinol,” Cancer Research 54: 1446-1449. |
Michnovicz et al. (1997), “Changes in Levels of Urinary Estrogen Metabolites After Oral Indole-3-carbinol Treatment in Humans, ” Journal of the National Cancer Institute 89(10):718-723. |