1999年9月
Studies aimed at enhancement of reactivity and enantioselectivity of a lithium ester enolate using a chiral tridentate lithium amide
TETRAHEDRON
- ,
- ,
- 巻
- 55
- 号
- 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
- ID情報
-
- DOI : 10.1016/S0040-4020(99)00644-4
- ISSN : 0040-4020
- CiNii Articles ID : 30004214297
- Web of Science ID : WOS:000082283600006