Competing Michael and Knoevenagel reactions of terpenoids with malononitrile on basic Cs-beta zeolite

被引:30
|
作者
Volcho, KP
Kurbakova, SY
Korchagina, DV
Suslov, EV
Salakhutdinov, NF
Toktarev, AV
Echevskii, GV
Barkhash, VA
机构
[1] Novosibirsk Organ Chem Inst, Novosibirsk 630090, Russia
[2] Boreskov Inst Catalysis, Novosibirsk 630090, Russia
关键词
basic zeolite; Michael reaction; Knoevenagel reaction; terpenoids; tandem reactions;
D O I
10.1016/S1381-1169(02)00581-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Basic cesium-beta (Cs-beta) zeolite has been synthesized. It proved to be an effective catalyst in reactions of a number of alpha,beta-unsaturated carbonyl compounds with malononitrile. It is shown that the process is either the Michael or Knoevenagel reaction, or tandem transformations generally initiated by the Michael reaction, which depends on steric hindrance at the carboryl group and the beta-position of the carbon=carbon (C=C) double bond adjacent to the carbonyl group. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:263 / 274
页数:12
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