Reductive Oxy-Nazarov Cyclization toward Expedient Construction of a Cyclopenta[1,2-b]pyrrolo[1,2-a]azepine Ring System: Formal Total Syntheses of Stemonamine and Cephalotaxine
Author:
Affiliation:
1. School of Chemistry, Key Laboratory of Advanced Technologies of Material, Minister of Education, School of Life Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan 610031, P. R. China
Funder
Natural Science Foundation of Sichuan Province
Fundamental Research Funds for the Central Universities
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00035
Reference52 articles.
1. X-Ray crystallographic determination of the structure of stemonamine, a new alkaloid from Stemona japonica miq.: isolation of isostemonamine
2. Recent progress in the chemistry of the Stemona alkaloids
3. Strategies for the synthesis of Stemona alkaloids: an update
4. Recent advances in the transformations of different types of Stemona alkaloids
5. The structure and bioactivities of Stemona alkaloids and alkaloids with [1,2-α] azepine nucleus (2009–2021)
Cited by 2 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. Bioinspired Total Synthesis of 3-epi-Junipercedrol;Organic Letters;2024-08-27
2. Correction to “Reductive Oxy-Nazarov Cyclization toward Expedient Construction of a Cyclopenta[1,2-b]pyrrolo[1,2-a]azepine Ring System: Formal Total Syntheses of Stemonamine and Cephalotaxine”;The Journal of Organic Chemistry;2024-05-24
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