Lewis Acid-Promoted Cross Aldol Reaction of Aldehydes with Ketones Utilizing 3-Methyl-2-phenyl-2-(2-oxoalkyl)benzothiazolines as an Enolate-Transferring Reagent-Reference-Cited by-同舟云学术

Lewis Acid-Promoted Cross Aldol Reaction of Aldehydes with Ketones Utilizing 3-Methyl-2-phenyl-2-(2-oxoalkyl)benzothiazolines as an Enolate-Transferring Reagent

Published:1990-02 Issue:2 Volume:63 Page:497-501
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Chikashita Hidenori,Tame Shin-ichiro,Yamada Seiji,Itoh Kazuyoshi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/63/2/63_2_497/_pdf

Reference18 articles.

1. AlCl3-Promoted Conjugate Reduction of α,β Unsaturated Carbonyl Compounds with 1,3-Dimethyl-2-phenylbenzimidazoline

2. In Situ Generation and Synthetic Application of 2-Phenylbenzimidazoline to the Selective Reduction of Carbon–Carbon Double Bonds of Electron-Deficient Olefins

3. 1,3-Dimethyl-2-phenylbenzimidazoline as a novel and efficient reagent for mild reductive dehalogenation of .alpha.-halo carbonyl compounds and acid chlorides

4. New method for the facile reduction of .alpha.-nitro sulfones to nitroalkanes via an electron-transfer-hydrogen atom abstraction mechanism

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4. Volume 3 References;Comprehensive Heterocyclic Chemistry II;1996

5. Thiazoles;Comprehensive Heterocyclic Chemistry II;1996