Useful reactions in modern pheromone synthesis

被引：30

作者：

Mori, K

Tashiro, T

机构：

[1] Fuji Flavor Co Ltd, Insect Pheromone & Traps Div, Tokyo 2058503, Japan

[2] Tokyo Univ Sci, Dept Chem, Shinjuku Ku, Tokyo 1628601, Japan

来源：

CURRENT ORGANIC SYNTHESIS | 2004年 / 1卷 / 01期

关键词：

asymmetric dihydroxylation; biocatalysis; isoprenoidal pheromones; olefin metathesis; pheromone acetals; pheromone epoxides;

D O I：

10.2174/1570179043485466

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Various aspects of pheromone synthesis are reviewed by analyzing examples published between 1990 and early 2003. Syntheses executed with new methodologies such as organoborane reactions, organotransition metal chemistry including olefin metathesis, asymmetric epoxidation, asymmetric dihydroxylation, other asymmetric chemical processes, and stereoselective biocatalysis are selected to illustrate the usefulness of new reactions in pheromone synthesis.

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收藏

页码：11 / 29

页数：19

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