| ID | 56204 |
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| Author |
Takamura, Hiroyoshi
Department of Chemistry, Graduate School of Natural Science and Technology, Okayama University
ORCID
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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
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| 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.
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| 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).
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| Published Date | 2016-05-06
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| Publication Title |
Organic Letters
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| Volume | volume18
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| Issue | issue9
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| Publisher | American Chemical Society
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| Start Page | 2110
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| End Page | 2113
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| ISSN | 15237060
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| NCID | AA11347843
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| Content Type |
Journal Article
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| language |
英語
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| OAI-PMH Set |
岡山大学
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| File Version | author
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| Related Url | isVersionOf https://doi.org/10.1021/acs.orglett.6b00737
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