Synthesis of the 2,2′:3′,3′':2′',2′'' tetraindole framework of the alkaloid bisindigotin
Author:
Funder
University of Auckland
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference48 articles.
1. Synthetic Studies toward Bisindigotin: Polyheteroaromatic Scaffolds via Skeletal Rearrangements of a Diacetoxytetraindole;Prystupa;J. Org. Chem.,2021
2. Octacycles and Nonacycles from 3-Hydroxy-2,2′-Bisindole;Prystupa;J. Org. Chem.,2021
3. 2,2ʹ-Bisindole can be accessed in one-step from indigo, but is accompanied by substantial quantities of other reduction products: (a) Somei, M.; Hayashi, H.; Izumi, T.; Ohmoto, S. Simple Synthesis of 2,2'-Bisindole from Indigo and Its Application for the Syntheses of Indole[2,3-a]Pyrrolo[3,4-c]Carbazole-5,7-(6H)Dione and -5-(6)-One Derivatives. Heterocycles 1995, 41 (10), 2161-2164;
4. Ohmoto, S. Reduction of Indigo: Simple Synthesis of 3-Acetoxy-, 1-Acetyl-2,3-Dihydro-, 3-Acetoxy-3'-Acetyl-, 3-Acetoxy-1,3'-Diacetyl-2,2'-Bisindoles, and 2,2'-Bisindole. Heterocycles 1997, 44 (1), 169-176.
5. (a) Somei, M.; Hayashi, H.; Izumi, T.; Ohmoto, S. Simple Synthesis of 2,2'-Bisindole from Indigo and Its Application for the Syntheses of Indole[2,3-a]Pyrrolo[3,4-c]Carbazole-5,7-(6H)Dione and -5-(6)-One Derivatives. Heterocycles 1995, 41 (10), 2161-2164;
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