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