A Convenient Synthesis of (r)-Japonilure
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919008052841
Reference7 articles.
1. Identification of the Female Japanese Beetle Sex Pheromone: Inhibition of Male Response by an Enantiomer
2. Asymmetric synthesis of (R,Z)-(-)-5-(1-decenyl)oxacyclopentan-2-one, the pheromone of the Japanese beetle.
3. Syntheses of chiral .GAMMA.-lactones from D-and L-arabinoses.
4. L(+)Propylene Glycol
5. Efficient Synthesis of (R)-(—)-g-Benzyloxymethyl-g-butyrolactone from (D)-(+)-Mannitol
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1. Catalytic asymmetric synthesis of Japonilure and its enantiomer;Tetrahedron: Asymmetry;2014-10
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3. Synthesis of enantiomericaly pure γ-lactones from 2,3-O-isopropylidene-D- or L-erythrose;Arkivoc;2009-05-29
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5. Unexpected Stereochemistry in the Lithium Salt Catalyzed Ring Expansion of Nonracemic Oxaspiropentanes. Formal Syntheses of (−)-(4R,5R)-Muricatacin and the Pheromone (R)-Japonilure;Organic Letters;2003-07-12
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