Stereospecific inversion of secondary tosylates to yield chiral methyl-branched building blocks, applied to the asymmetric synthesis of leafminer sex pheromones-Reference-Cited by-同舟云学术

Stereospecific inversion of secondary tosylates to yield chiral methyl-branched building blocks, applied to the asymmetric synthesis of leafminer sex pheromones

Published:2012-06 Issue:11-12 Volume:23 Page:852-858
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Taguri Tomonori,Yamakawa Rei,Fujii Toru,Muraki Yuta,Ando Tetsu

Publisher

Elsevier BV

Subject

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

Reference27 articles.

1. Ando, T. Internet database 2011. http://www.tuat.ac.jp/~antetsu/LepiPheroList.htm.

2. El-Sayed, A. M. Internet database 2011. http://www.pherobase.com/.

3. Lepidopteran Sex Pheromones

4. Positions and Stereochemistry of Methyl Branches in the Novel Sex Pheromone Components Produced by a Lichen Moth, Lyclene dharma dharma

5. (5R,7R)-5-Methylheptadecan-7-ol: a novel sex pheromone component produced by a female lichen moth, Miltochrista calamina, in the family Arctiidae

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