Hydrolytic kinetic resolution of terminal mono- and bis-epoxides in the synthesis of insect pheromones: routes to (−)-( R )- and (+)-( S )-10-methyldodecyl acetate, (−)-( R )-10-methyl-2-tridecanone, (−)-( R )-( Z )-undec-6-en-2-ol (Nostrenol), (−)-(1 R ,7 R )-1,7-dimethylnonyl propanoate, (−)-(6 R ,12 R )-6,12-dimethylpentadecan-2-one, (−)-(2 S ,11 S )-2,11-diacetoxytridecane and (+)-(2 S ,12 S )-2,12-diacetoxytridecane-Reference-Cited by-同舟云学术

Hydrolytic kinetic resolution of terminal mono- and bis-epoxides in the synthesis of insect pheromones: routes to (−)-( R )- and (+)-( S )-10-methyldodecyl acetate, (−)-( R )-10-methyl-2-tridecanone, (−)-( R )-( Z )-undec-6-en-2-ol (Nostrenol), (−)-(1 R ,7 R )-1,7-dimethylnonyl propanoate, (−)-(6 R ,12 R )-6,12-dimethylpentadecan-2-one, (−)-(2 S ,11 S )-2,11-diacetoxytridecane and (+)-(2 S ,12 S )-2,12-diacetoxytridecane

Published:2002-05 Issue:7 Volume:13 Page:779-793
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Chow Sharon,Kitching William

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference42 articles.

1. For a semi-encyclopedic compilation for the period 1979–1989, see Mori, K. In The Total Synthesis of Natural Products; Simon, J. A., Ed.; John Wiley and Sons Inc.: Brisbane, Australia, 1992; Vol. 9

2. Enantioselective synthesis of bioactive natural products

3. Chirality and insect pheromones

4. Pheromones: synthesis and bioactivity

5. Semiochemicals – Synthesis, Stereochemistry, and Bioactivity

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