Stereoselective synthesis of the left wing of Caribbean ciguatoxin-Reference-Cited by-同舟云学术

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Stereoselective synthesis of the left wing of Caribbean ciguatoxin

Published:2011-09 Issue:35 Volume:67 Page:6616-6626
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Yamashita Shuji,Uematsu Ryohei,Hirama Masahiro

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference69 articles.

1. The changing face of ciguatera

2. Marine toxins

3. Tetrahedron perspective number 2

4. A survey of comparative toxicity in the food chain of ciguatera.

5. Structures of ciguatoxin and its congener

Cited by 14 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. Synthesis of the MN Ring of Caribbean Ciguatoxin C-CTX-1 via Desymmetrization by Acetal Formation;Organic Letters;2024-01-19

2. Convergent and Scalable Synthesis of the ABCDE-Ring Fragment of Caribbean Ciguatoxin C-CTX-1;The Journal of Organic Chemistry;2022-12-20

3. Convergent Synthesis of the HIJKLMN-Ring Fragment of Caribbean Ciguatoxin C-CTX-1 by a Late-Stage Reductive Olefin Coupling Approach;Bulletin of the Chemical Society of Japan;2022-05-15

4. Unified Synthesis of the DEF and GHI Ring Systems of Maitotoxin;Chemistry Letters;2019-09-05

5. First stereo selective synthesis of 5-O-feruloyl-2-deoxy-d-ribono-γ-lactone;Tetrahedron Letters;2016-10

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