Direct, four-step synthetic pathway to iheyamine A and several analogues
Author:
Affiliation:
1. State Key Laboratory of Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang 550014, China
2. Key Laboratory of Chemistry for Natural Products of Guizhou Province, Chinese Academy of Sciences, Guiyang 550014, China
Abstract
Funder
Science and Technology Program of Guizhou Province
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB00397J
Reference24 articles.
1. Non-monoterpenoid azepinoindole alkaloids
2. Iheyamines, new cytotoxic bisindole pigments from a colonial ascidian, Polycitorella sp.
3. Three New Indole Alkaloids from Trigonostemon lii
4. A Compact Approach to an Isomeric Iheyamine A System and X-ray Crystal Structure of 5-Methyl-5H-azepino[2,3- b :4,5- b ′]diindole
5. Synthesis of the Azepinobisindole Alkaloid Iheyamine A Enabled by a Cross-Mannich Reaction
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