Synthesis of the pheromone components of the grape borer Xylotrechus pyrrhoderus by microbiological reduction of an α-diketone

In a continuation of our investigation on the preparation of chiral hydroxy synthons by microbial reduction of the corresponding mono- or diketones, we have carried out a study on the reduction of alpha -diketones.

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Bibliographic Details
Published inJournal of organic chemistry Vol. 54; no. 13; pp. 3221 - 3223
Main Authors BEL-RHLID, R, FAUVE, A, VESCHAMBRE, H
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 01.06.1989
Subjects
alpha -diketone
Bioconversions. Hemisynthesis
Biological and medical sciences
biological control
Biotechnology
Cerambycidae
Coleoptera
Fundamental and applied biological sciences. Psychology
Methods. Procedures. Technologies
Xylotrechus pyrrhoderus
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Summary:In a continuation of our investigation on the preparation of chiral hydroxy synthons by microbial reduction of the corresponding mono- or diketones, we have carried out a study on the reduction of alpha -diketones.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0022-3263
1520-6904
DOI:10.1021/jo00274a053