Total Synthesis of (-)-(7S,10R)-Calamenene and (-)-(7S,10R)-2-Hydroxycalamenene by Use of a Ring-Closing Metathesis Reaction. A Comparison of the cis- and trans-Isomers-Reference-Cited by-同舟云学术

Total Synthesis of (-)-(7S,10R)-Calamenene and (-)-(7S,10R)-2-Hydroxycalamenene by Use of a Ring-Closing Metathesis Reaction. A Comparison of the cis- and trans-Isomers

Published:2002-07-31 Issue:7 Volume:7 Page:517-527
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Nakashima Katsuyuki,Imoto Masashi,Sono Masakazu,Tori Motoo,Nagashima Fumihiro,Asakawa Yoshinori

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/7/7/517/pdf

Reference20 articles.

1. The absolute stereochemistry of the calamenenes

2. (+)-8-Hydroxycalamenene: A fish-poison principle of Dysoxylum acutangulum and D. Alliaceum

3. Absolute configuration of the (+)-calamenenes: crystal structure of 7-hydroxycalamenene

4. Progress in the Chemistry of Organic Natural Products;Asakawa,1982

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