Rapid Total Synthesis of Iheyamine A via a Pictet–Spengler/Redox-Mediated Cyclization Cascade-Reference-Cited by-同舟云学术

Rapid Total Synthesis of Iheyamine A via a Pictet–Spengler/Redox-Mediated Cyclization Cascade

Published:2023-03-23 Issue:7 Volume:88 Page:4814-4817
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wu Ya¹,Wang Ming¹,Xu Mei¹,Liu Sheng¹^ORCID

Affiliation:

1. State Key Laboratory of Functions and Applications of Medicinal Plants, Guizhou Medical University; The Key Laboratory of Chemistry for Natural Products of Guizhou Province and Chinese Academy of Science, Guiyang 550031, China

Funder

Natural Science Foundation of Guizhou Province

Science and Technology Foundation of Guizhou Province

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c03060

Reference23 articles.

1. Iheyamines, new cytotoxic bisindole pigments from a colonial ascidian, Polycitorella sp.

2. 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

3. Synthesis of the Azepinobisindole Alkaloid Iheyamine A Enabled by a Cross-Mannich Reaction

4. Observations arising from a Beckmann rearrangement-Mannich cyclization approach to the azepinobisindole alkaloid iheyamine A

5. Dehydrative Mannich-Type Reaction for the Synthesis of Azepinobisindole Alkaloid Iheyamine A

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3. Recent Progress Toward Total Syntheses of Iheyamines A and B;Asian Journal of Organic Chemistry;2024-01-11

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