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Mendeleev Communications, 1994, Volume 4, Issue 2, Pages 40–41
DOI: https://doi.org/10.1070/MC1994v004n02ABEH000338
(Mi mendc5142)
 

This article is cited in 3 scientific papers (total in 3 papers)

A Chemico-Enzymatic Synthesis of All Four Stereoisomers of 1,6-Dimethyloct-1-yl Formate, an Aggregation Pheromone Mimic for the Smaller Flour Beetle

G. D. Gamalevich, E. P. Serebryakov

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (277 kB) Citations (3)
Abstract: (2R,6R)-, (2R,6S)-, (2S,6R)- and (2S,6S)-2,6-dimethyloct-1 -yl formates have been prepared from S-(+)- and R-(–)-enantiomers of 3,7-dimethylocta-1,6-diene via enantioselective hydrolysis of (2R/S,6R)- and (2R/S,6S)-2,6-dimethyloct-1-yl formates with porcine pancreatic lipase as the key step.
Bibliographic databases:
Document Type: Article
Language: English


Citation: G. D. Gamalevich, E. P. Serebryakov, “A Chemico-Enzymatic Synthesis of All Four Stereoisomers of 1,6-Dimethyloct-1-yl Formate, an Aggregation Pheromone Mimic for the Smaller Flour Beetle”, Mendeleev Commun., 4:2 (1994), 40–41
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