The Reaction of Cyclopropyl Ketones with Acetyl Methanesulfonate. An efficient ring opening under neutral conditions with regiospecific enol acetate formation and stereo-controlled nucleophilic addition. Preliminary communication-Reference-Cited by-同舟云学术

The Reaction of Cyclopropyl Ketones with Acetyl Methanesulfonate. An efficient ring opening under neutral conditions with regiospecific enol acetate formation and stereo-controlled nucleophilic addition. Preliminary communication

Published:1979-10-31 Issue:7 Volume:62 Page:2338-2340
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Demuth Martin,Raghavan Palaykotai R.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference14 articles.

1. Electrophilic cyclopropanes in organic synthesis

2. Recent studies on the synthesis of natural products

3. Synthesis, spectral properties, and chemical ring opening of tricyclo[3,3.0.02,8]octan-3-one, a rigid model for unsymmetrical cyclopropyl ketone participation

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