The Stereochemistry of Nucleophilic Addition. IV. The Condensation of 2,2,6-Trimethylcyclohexanone witht-Butyl Acetate in the Presence of Lithium Amide-Reference-Cited by-同舟云学术

The Stereochemistry of Nucleophilic Addition. IV. The Condensation of 2,2,6-Trimethylcyclohexanone witht-Butyl Acetate in the Presence of Lithium Amide

Published:1972-04 Issue:4 Volume:45 Page:1147-1152
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Matsumoto Takashi,Sakata Gojo,Tachibana Yakudo,Fukui Kenji

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/45/4/45_4_1147/_pdf

Reference15 articles.

1. The Stereochemistry of Nucleophilic Addition. I. The Reformatsky Reaction of 2-Methyl- and 2-Ethylcyclohexanones

2. The Stereochemistry of Nucleophilic Addition. II. The Reformatsky Reaction of Methyl (+)-α-Bromopropionate, 2-Phenylpropanal, and 3-Phenyl-2-butanone

3. β-HYDROXY ESTERS FROM KETONES AND ESTERS

4. Aldol Condensation of Esters with Ketones or Aldehydes to Form β-Hydroxy Esters by Lithium Amide. Comparison with the Reformatsky Reaction1

5. Role of Metallic Cation in Aldol Condensation of Metallo Esters with Acetophenone to Form β-Hydroxy Esters. Reversal to Claisen Acylation or Self-condensation of the Ketone1

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