A short, stereodivergent synthesis of the racemic erythro and threo diastereomers of 6-acetoxy-5-hexadecanolide, a mosquito oviposition attractant pheromone-Reference-Cited by-同舟云学术

A short, stereodivergent synthesis of the racemic erythro and threo diastereomers of 6-acetoxy-5-hexadecanolide, a mosquito oviposition attractant pheromone

Published:1986-01 Issue:34 Volume:27 Page:4011-4014
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Jefford Charles W.,Jaggi Danielle,Boukouvalas John

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference30 articles.

1. Synthesis of both the enantiomers of erythro-6-acetoxy-5-hexadecanolide

2. ENANTIOSPECIFIC SYNTHESIS OF (+)-ERYTHRO-(5S,6R)-6-ACETOXY-5-HEXADECANOLIDE, AN OPTICALLY ACTIVE FORM OF THE MAJOR COMPONENT OF A MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE

3. SYNTHESIS OF BOTH ENANTIOMERS OF ERYTHRO-6-ACETOXY-5-HEXADECANOLIDE, THE MAJOR COMPONENT OF A MOSQUITO OVIPOSITION ATTRACTANT PHEROMONE

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