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Enantioselective synthesis of Anomala osakana pheromone and Janus integer pheromone: a flexible approach to chiral gamma-butyrolactones.

Authors :
Lin L
Zhao Q
Li AN
Ren F
Yang F
Wang R
Source :
Organic & biomolecular chemistry [Org Biomol Chem] 2009 Sep 21; Vol. 7 (18), pp. 3663-5. Date of Electronic Publication: 2009 Jul 31.
Publication Year :
2009

Abstract

The enantioselective synthesis of Anomala osakana pheromone and Janus integer pheromone has been achieved without using any protecting groups. The synthesis involved using an asymmetric alkynylation to obtain gamma-hydroxy-alpha,beta-acetylenic esters with high ee (84%) and yields ( approximately 80%), followed by selective hydrogenation and lactonization in high overall yields (87% and 89%).

Details

Language :
English
ISSN :
1477-0539
Volume :
7
Issue :
18
Database :
MEDLINE
Journal :
Organic & biomolecular chemistry
Publication Type :
Academic Journal
Accession number :
19707669
Full Text :
https://doi.org/10.1039/b909418k