Synthesis of (R)-ar-turmerone and its conversion to (R)-ar-himachalene, a pheromone component of the flea beetle: (R)-ar-himachalene is dextrorotatory in hexane, while levorotatory in chloroform-Reference-Cited by-同舟云学术

Synthesis of (R)-ar-turmerone and its conversion to (R)-ar-himachalene, a pheromone component of the flea beetle: (R)-ar-himachalene is dextrorotatory in hexane, while levorotatory in chloroform

Published:2005-02 Issue:3 Volume:16 Page:685-692
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Mori Kenji

Publisher

Elsevier BV

Subject

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

Reference27 articles.

1. Total Synthesis of Himachalene Sesquiterpenes ofAphthonaandPhyllotretaFlea Beetles

2. Synthesis and Stereochemistry of the Four Himachalene-Type Sesquiterpenes Isolated from the Flea Beetle (Aphthona flava) as Pheromone Candidates

3. Synthesis of optically active pheromones

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