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. An account on pyranosylated and furanosylated indolocarbazole natural products;Tetrahedron;2024-08
2. Design and Synthesis of Diphosphine Ligands Based on the Chiral Biindolyl Scaffold and Their Application in Transition-Metal Catalysis;Organic Letters;2024-02-16
3. Recent Progress Toward Total Syntheses of Iheyamines A and B;Asian Journal of Organic Chemistry;2024-01-11
4. Total Syntheses of 2,2′-Biindolyl Alkaloids via Cyanide-Catalyzed Imino-Stetter Reaction;Synlett;2023-04-05
5. Synthesis of the 2,2′:3′,3′':2′',2′'' tetraindole framework of the alkaloid bisindigotin;Tetrahedron Letters;2022-09
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