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Pheromone synthesis, CXVIII. Synthesis of the enantiomers of (E)‐1‐ethyl‐5‐methyl‐4‐heptenyl acetate (quadrilure), the aggregation pheromone of Cathartus quadricollis

Pheromone synthesis, CXVIII. Synthesis of the enantiomers of (E)‐1‐ethyl‐5‐methyl‐4‐heptenyl... The synthesis of (R)‐ and (S)‐quadrilure (1) was achieved starting from (R)‐ and (S)‐methyl 3‐hydroxypentanoate (2) in 8 steps (34–35% yield). http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png European Journal of Organic Chemistry Wiley

Pheromone synthesis, CXVIII. Synthesis of the enantiomers of (E)‐1‐ethyl‐5‐methyl‐4‐heptenyl acetate (quadrilure), the aggregation pheromone of Cathartus quadricollis

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References (13)

Publisher
Wiley
Copyright
Copyright © 1990 Wiley Subscription Services, Inc., A Wiley Company
ISSN
1434-193X
eISSN
1099-0690
DOI
10.1002/jlac.199019900127
Publisher site
See Article on Publisher Site

Abstract

The synthesis of (R)‐ and (S)‐quadrilure (1) was achieved starting from (R)‐ and (S)‐methyl 3‐hydroxypentanoate (2) in 8 steps (34–35% yield).

Journal

European Journal of Organic ChemistryWiley

Published: Dec 12, 1990

Keywords: ; ; ; ;

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