2,2′-Biindolyl revisited. Synthesis and reactions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference43 articles.
1. Synthesis of indolo[2,3-a]pyrrolo[3,4-c]carbazoles by double Fischer indolizations
2. Coupling of indoleacetic acid trianion or methyl indoleacetic acid dianion. A biomimetic approach to indolocarbazole alkaloids.
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1. Recent Progress Toward Total Syntheses of Iheyamines A and B;Asian Journal of Organic Chemistry;2024-01-11
2. Total Syntheses of 2,2′-Biindolyl Alkaloids via Cyanide-Catalyzed Imino-Stetter Reaction;Synlett;2023-04-05
3. Synthesis of the 2,2′:3′,3′':2′',2′'' tetraindole framework of the alkaloid bisindigotin;Tetrahedron Letters;2022-09
4. Seven-Membered Rings With Three Heteroatoms 1,3,5;Comprehensive Heterocyclic Chemistry IV;2022
5. An account of synthetic strategies towards indolocarbazole alkaloids: Arcyriaflavin A and staurosporinone;Tetrahedron;2021-02
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