MISC

2004年8月

A new approach to the synthesis of cyclic ethers via the intermolecular allylation of alpha-acetoxy ethers and ring-closing metathesis

TETRAHEDRON
  • Kadota, I
  • ,
  • H Uyehara
  • ,
  • Y Yamamoto

60
34
開始ページ
7361
終了ページ
7365
記述言語
英語
掲載種別
DOI
10.1016/j.tet.2004.05.045
出版者・発行元
PERGAMON-ELSEVIER SCIENCE LTD

A concise synthesis of the isolaurepinnacin skeleton 6 was achieved via the intermolecular allylation of the alpha-acetoxy ether 3 followed by ring-closing metathesis. This methodology was successfully applied to the convergent synthesis of the oxocene 15, an advanced synthetic intermediate for the total synthesis of laurencin. (C) 2004 Elsevier Ltd. All rights reserved.

Web of Science ® 被引用回数 : 24

リンク情報
DOI
https://doi.org/10.1016/j.tet.2004.05.045
CiNii Articles
http://ci.nii.ac.jp/naid/80016808067
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000223090800027&DestApp=WOS_CPL

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