Highly stereocontrolled synthesis of (2E,4Z)-dienoic esters with alumina catalyst. Its application to total syntheses of flavor components and insect pheromones
- 1 November 1982
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 47 (23) , 4478-4482
- https://doi.org/10.1021/jo00144a015
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Reaction of copper enolates of esters with propargylic systems. Facile preparation of 3,4-dienoic esters, stereoselective rearrangement to (2E,4Z)- and (2E,4E)-dienoic esters, and stereoselective synthesis of a fragrance from the Bartlett pearThe Journal of Organic Chemistry, 1978
- The synthesis of insect sex phermonesTetrahedron, 1977
- Pheromone synthesis. 4. A synthesis of (.+-.)-methyl n-tetradeca-trans-2,4,5-trienoate, an allenic ester produced by the male dried bean beetle Acanthoscelides obtectus (Say)The Journal of Organic Chemistry, 1977