MISC

1999年7月

A novel synthesis of chiral tetrahydroisoquinolines employing silyl enol ethers in the presence of chiral acyl chlorides

SYNLETT
  • T Itoh
  • ,
  • K Nagata
  • ,
  • M Miyazaki
  • ,
  • A Ohsawa

1999
7
開始ページ
1154
終了ページ
1156
記述言語
英語
掲載種別
出版者・発行元
GEORG THIEME VERLAG

6,7-Dimethoxyisoquinoline derivatives reacted with silyl enol ethers in a highly diastereoselective manner in the presence of an acyl chloride derived from L-alanine. (-)-Homolaudanosine was synthesized in an enantiopure form from 6,7-dimethoxyisoquinoline via six steps using this method.

リンク情報
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000081954300044&DestApp=WOS_CPL
ID情報
  • ISSN : 0936-5214
  • Web of Science ID : WOS:000081954300044

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