A convenient method for the synthesis of (E)-3-alkenoic acids by a regio- and stereoselective reaction of β-vinyl-β-propiolactone with organocopper reagents-Reference-Cited by-同舟云学术

A convenient method for the synthesis of (E)-3-alkenoic acids by a regio- and stereoselective reaction of β-vinyl-β-propiolactone with organocopper reagents

Published:1981-01 Issue:19 Volume:22 Page:1817-1820
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Sato Toshio,Takeuchi Masashi,Itoh Toshiyuki,Kawashima Masatoshi,Fujisawa Tamotsu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Nucleophilic and organometallic displacement reactions of allylic compounds: stereo-and regiochemistry

2. A three carbon homologation by the ring-opening of β-propiolactones with diorganocuprates

3. COPPER-CATALYZED REACTION OF GRIGNARD REAGENTS WITH β-PROPIOLACTONES: A CONVENIENT METHOD FOR THE SYNTHESIS OF β-SUBSTITUTED PROPIONIC ACIDS

4. Reaction of ketene with aldehydes in the presence of zinc carboxylic acid salts

5. Catalytic ring opening of substituted 2-oxetanones

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