Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/23697
Title: 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
Issue Date: 2009
Publisher: Royal Society of Chemistry
Source: Organic & biomolecular chemistry, 2009, v. 7, no. 18, p. 3663-3665 How to cite?
Journal: Organic & biomolecular chemistry 
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 (similar to 80%), followed by selective hydrogenation and lactonization in high overall yields (87% and 89%).
URI: http://hdl.handle.net/10397/23697
ISSN: 1477-0520
EISSN: 1477-0539
DOI: 10.1039/b909418k
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