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ID 56204
フルテキストURL
著者
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
抄録
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.
備考
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).
発行日
2016-05-06
出版物タイトル
Organic Letters
18巻
9号
出版者
American Chemical Society
開始ページ
2110
終了ページ
2113
ISSN
15237060
NCID
AA11347843
資料タイプ
学術雑誌論文
言語
English
OAI-PMH Set
岡山大学
論文のバージョン
author
PubMed ID
DOI
Web of Sience KeyUT
関連URL
isVersionOf https://doi.org/10.1021/acs.orglett.6b00737