Synthesis of disparlure and monachalure enantiomers from 2,3-butanediacetals

Synthesis of disparlure and monachalure enantiomers from 2,3-butanediacetals

2,3-Butanediacetal derivatives were used for the stereoselective synthesis of unsymmetrically substituted cis-epoxides. The procedure was applied for the preparation of both enantiomers of disparlure and monachalure, the components of the sex pheromones of the gypsy moth (Lymantria dispar) and the n...

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Bibliographic Details
Main Authors: Adam Drop, Hubert Wojtasek, Bożena Frąckowiak-Wojtasek
Format: Article
Language:English
Published: Beilstein-Institut 2020-04-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
2,3-butanediacetal
cis-epoxide
(−)-disparlure
(+)-disparlure
(−)-monachalure
(+)-monachalure
Online Access:https://doi.org/10.3762/bjoc.16.57

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