A Concise, Protection-Free and Divergent Approach for the Enantioselective Syntheses of Two Pheromonal Epoxide Components of the Fall Webworm Moth and Other Species
Author:
Affiliation:
1. Department of Chemistry and Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian 361005, People's Republic of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo1007042
Reference35 articles.
1. Sex pheromone of the fall webworm moth,Hyphantria cunea
2. Identification of (3Z,6Z)-1,3,6–9,10-epoxyheneicosatriene and (3Z,6Z)-1,3,6–9,10-epoxyeicosatriene in the sex pheromone of hyphantria cunea
3. Sex pheromone of the saltmarsh caterpillar moth,Estigmene acrea
4. Pheromones of two arctiid moths (Creatonotos transiens andC. gangis)
5. Total synthesis of enantiomers of (3Z,6Z)-cis-9,10-epoxy 1,3,6-henicosatriene — the pheromonal component of Diacrisia obliqua
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2. Enantioselective Reaction;Organic Stereochemistry;2015-06-26
3. Practical Synthesis of (9S,10R)‐9,10‐epoxy‐(3Z,6Z)‐henicosadiene: The Major Pheromone of the Saltmarsh Caterpillar moth Estigmene acrea;Bulletin of the Korean Chemical Society;2015-03-17
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5. Scalable synthesis of the pink gypsy moth Lymantria mathura sex pheromone (–)-mathuralure;Canadian Journal of Chemistry;2013-03
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