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