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« Previous Abstract[Dichlorvos insect strips indoors: pollution and risk assessment]    Next Abstract"A general, asymmetric, and noniterative synthesis of trideoxypropionates. Straightforward syntheses of the pheromones (+)-vittatalactone and (+)-norvittatalactone" »

Chem Commun (Camb)


Title:"A non-iterative, flexible, and highly stereoselective synthesis of polydeoxypropionates--synthesis of (+)-vittatalactone"
Author(s):Weise CF; Pischl M; Pfaltz A; Schneider C;
Address:"Institut fur Organische Chemie, Universitat Leipzig, Johannisallee 29, D-04103 Leipzig, Germany"
Journal Title:Chem Commun (Camb)
Year:2011
Volume:20110128
Issue:11
Page Number:3248 - 3250
DOI: 10.1039/c0cc05215a
ISSN/ISBN:1364-548X (Electronic) 1359-7345 (Linking)
Abstract:"A short sequence comprising an oxy-Cope rearrangement, iridium-catalyzed hydrogenation, and enolate methylation provides trideoxypropionates with excellent diastereocontrol. A straightforward synthesis of the cucumber beetle pheromone (+)-vittatalactone illustrates this new strategy"
Keywords:Animals Catalysis Coleoptera/chemistry Hydrogenation Iridium/chemistry Lactones/*chemical synthesis/chemistry Pheromones/chemistry Stereoisomerism;
Notes:"MedlineWeise, Christian F Pischl, Matthias Pfaltz, Andreas Schneider, Christoph eng Research Support, Non-U.S. Gov't England 2011/02/01 Chem Commun (Camb). 2011 Mar 21; 47(11):3248-50. doi: 10.1039/c0cc05215a. Epub 2011 Jan 28"

 
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Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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