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ID 56204
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Takamura, Hiroyoshi Department of Chemistry, Graduate School of Natural Science and Technology, Okayama University
Kikuchi, Takahiro Department of Chemistry, Graduate School of Natural Science and Technology, Okayama University
Endo, Noriyuki Himeji EcoTech Co., Ltd.
Fukuda, Yuji Himeji EcoTech Co., Ltd.
Kadota, Isao Department of Chemistry, Graduate School of Natural Science and Technology, Okayama University
Abstract
The first total syntheses of sarcophytonolide H and the originally proposed and correct structures of isosarcophytonolide D have been achieved via transannular ring-closing metathesis (RCM). These total syntheses culminated in the stereostructural confirmation of sarcophytonolide H and the reassignment of isosarcophytonolide D, respectively. The antifouling activity of the synthetic sarcophytonolide H and its analogues was also evaluated.
Note
This is an Accepted Manuscript of an article published by American Chemical Society
This work was supported by Okayama Foundation for Science and Technology and JSPS KAKENHI (24710250).
Published Date
2016-05-06
Publication Title
Organic Letters
Volume
volume18
Issue
issue9
Publisher
American Chemical Society
Start Page
2110
End Page
2113
ISSN
15237060
NCID
AA11347843
Content Type
Journal Article
language
英語
OAI-PMH Set
岡山大学
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isVersionOf https://doi.org/10.1021/acs.orglett.6b00737