Total Syntheses of Iheyamines A and B
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
Funder
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.2c02583
Reference19 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. Dehydrative Mannich-Type Reaction for the Synthesis of Azepinobisindole Alkaloid Iheyamine A
4. Biomimetic Synthesis of Iheyamine A from Spirocyclic Oxindoles
5. Total Synthesis of Iheyamine A via the Cyanide-Catalyzed Imino-Stetter Reaction
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1. Synthesis, structural modification, and biological activity of a novel bisindole alkaloid iheyamine A;Bioorganic Chemistry;2024-12
2. A novel iheyamine A derivative L42 suppresses acute myeloid leukemia via dual regulation of the PI3K/AKT/FOXO3a axis and TNF signaling pathway;Biomedicine & Pharmacotherapy;2024-08
3. Diastereocontrolled Construction of Spiroindolenines via Hexafluoroisopropanol-Promoted Dearomative Epoxide–Indole Cyclization;Organic Letters;2024-01-25
4. Recent Progress Toward Total Syntheses of Iheyamines A and B;Asian Journal of Organic Chemistry;2024-01-11
5. Rapid Total Synthesis of Iheyamine A via a Pictet–Spengler/Redox-Mediated Cyclization Cascade;The Journal of Organic Chemistry;2023-03-23
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