Diastereoselective Brook Rearrangement-Mediated [3 + 4] Annulation: Application to a Formal Synthesis of (+)-Laurallene-Reference-Cited by-同舟云学术

Diastereoselective Brook Rearrangement-Mediated [3 + 4] Annulation: Application to a Formal Synthesis of (+)-Laurallene

Published:2008-04-08 Issue:9 Volume:10 Page:1803-1806
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Sasaki Michiko¹,Hashimoto Azusa¹,Tanaka Koudai¹,Kawahata Masatoshi¹,Yamaguchi Kentaro¹,Takeda Kei¹

Affiliation:

1. Department of Synthetic Organic Chemistry, Graduate School of Medical Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-Ku, Hiroshima 734-8553, Japan, and Tokushima Bunri University, Shido, Sanuki, Kagawa 769-2193, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol8003595

Reference34 articles.

1. Laurallene, new bromoallene from the marine red alga Yamada

2. Total Synthesis of (+)-Prelaureatin and (+)-Laurallene

3. Total synthesis of (+)-laurallene

4. Synthesis of Prelaureatin, Laurencin, and the Medium-Ring Ether Parts of Ciguatoxins

5. Total Synthesis of Prelaureatin

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