Convergent Synthesis of the HIJKLMN-Ring Fragment of Caribbean Ciguatoxin C-CTX-1 by a Late-Stage Reductive Olefin Coupling Approach
Author:
Affiliation:
1. Graduate School of Life Sciences, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, Miyagi 980-8577, Japan
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/bcsj.20220070
Reference82 articles.
1. The changing face of ciguatera
2. The chemistry and biological function of natural marine toxins
3. Tetrahedron perspective number 2
4. Marine toxins
5. Ciguatera Mini Review: 21st Century Environmental Challenges and the Interdisciplinary Research Efforts Rising to Meet Them
Cited by 3 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. Total Synthesis of (−)-Irijimaside A Enabled by Ni/Zr-Mediated Reductive Ketone Coupling;Organic Letters;2024-05-15
2. Synthesis of the MN Ring of Caribbean Ciguatoxin C-CTX-1 via Desymmetrization by Acetal Formation;Organic Letters;2024-01-19
3. Convergent and Scalable Synthesis of the ABCDE-Ring Fragment of Caribbean Ciguatoxin C-CTX-1;The Journal of Organic Chemistry;2022-12-20
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