Transformation of Esters into 2-Substituted Allyl Halides via Tertiary Cyclopropanols: Application in the Stereoselective Synthesis of (2S,3S,7S)-3,7-Dimethyl-2-pentadecyl Acetate, the Sex Pheromone of the Pine SawflyNeodiprion sertifer-Reference-Cited by-同舟云学术

Transformation of Esters into 2-Substituted Allyl Halides via Tertiary Cyclopropanols: Application in the Stereoselective Synthesis of (2S,3S,7S)-3,7-Dimethyl-2-pentadecyl Acetate, the Sex Pheromone of the Pine SawflyNeodiprion sertifer

Published:2006-11 Issue:22 Volume:2006 Page:5069-5075
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Bekish Andrei V.,Prokhorevich Konstantin N.,Kulinkovich Oleg G.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference80 articles.

1. Pheromones: synthesis and bioactivity

2. Chirality and insect pheromones

3. Useful Reactions in Modern Pheromone Synthesis

4. Sex Pheromone Specificity in the Pine Sawflies: Interchange of Acid Moieties in an Ester

5. Response of Male Jack Pine Sawfly, Neodiprion pratti banksianae (Hymenoptera: Diprionidae), to Mixtures of Optical Isomers of the Sex Pheromone, 3, 7-Dimethylpentadecan-2-ol

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