MISC

1999年9月

Studies aimed at enhancement of reactivity and enantioselectivity of a lithium ester enolate using a chiral tridentate lithium amide

TETRAHEDRON
  • MA Hussein
  • ,
  • A Iida
  • ,
  • K Tomioka

55
37
開始ページ
11219
終了ページ
11228
記述言語
英語
掲載種別
DOI
10.1016/S0040-4020(99)00644-4
出版者・発行元
PERGAMON-ELSEVIER SCIENCE LTD

Tridentate chiral amines 7-13 mediated the asymmetric condensation reaction of lithium ester enolate 2 with benzaldehyde p-anisidine imine 3 giving the corresponding beta-lactam 4 in UP to 75% ee. It became apparent that coexistence of 2 and chiral lithium amides derived from 7-13 is an important factor for the enhancement of the reactivity and enantioselectivity of 2. (C) 1999 Elsevier Science Ltd. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/S0040-4020(99)00644-4
CiNii Articles
http://ci.nii.ac.jp/naid/30004214297
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000082283600006&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/S0040-4020(99)00644-4
  • ISSN : 0040-4020
  • CiNii Articles ID : 30004214297
  • Web of Science ID : WOS:000082283600006

エクスポート
BibTeX RIS