Observations arising from a Beckmann rearrangement-Mannich cyclization approach to the azepinobisindole alkaloid iheyamine A
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference38 articles.
1. Iheyamines, new cytotoxic bisindole pigments from a colonial ascidian, Polycitorella sp.
2. Synthesis of the Azepinobisindole Alkaloid Iheyamine A Enabled by a Cross-Mannich Reaction
3. For the synthesis of 3-amidoindoles using the Beckmann rearrangement, see:
4. A versatile synthetic route to 11H-indolo[3,2-c]isoquinolines
Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Recent Progress Toward Total Syntheses of Iheyamines A and B;Asian Journal of Organic Chemistry;2024-01-11
2. Rapid Total Synthesis of Iheyamine A via a Pictet–Spengler/Redox-Mediated Cyclization Cascade;The Journal of Organic Chemistry;2023-03-23
3. Total Syntheses of Iheyamines A and B;J ORG CHEM;2023
4. Total Syntheses of Iheyamines A and B;The Journal of Organic Chemistry;2022-12-29
5. Asymmetric Total Synthesis of Iheyamine B;Organic Letters;2022-09-28
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