An Unusual Terpene Cyclization Mechanism Involving a Carbon-Carbon Bond Rearrangement-Reference-Cited by-同舟云学术

An Unusual Terpene Cyclization Mechanism Involving a Carbon-Carbon Bond Rearrangement

Published:2015-02-16 Issue:14 Volume:54 Page:4353-4356
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Meguro Ayuko,Motoyoshi Yudai,Teramoto Kazuya,Ueda Shota,Totsuka Yusuke,Ando Yumi,Tomita Takeo,Kim Seung-Young,Kimura Tomoyuki,Igarashi Masayuki,Sawa Ryuichi,Shinada Tetsuro,Nishiyama Makoto,Kuzuyama Tomohisa

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference24 articles.

1. Cyclooctatin, a new inhibitor of lysophospholipase, produced by Streptomyces melanosporofaciens MI614-43F2. Taxonomy, production, isolation, physico-chemical properties and biological activities.

2. The structure of cyclooctatin, a new inhibitor of lysophospholipase.

3. Cloning and Heterologous Expression of the Cyclooctatin Biosynthetic Gene Cluster Afford a Diterpene Cyclase and Two P450 Hydroxylases

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