Determination of the absolute configuration at C-6 and C-7 of serricornin (4,6-dimethyl-7-hydroxy-3-nonanone), the sex pheromone of the cigarette beetle-Reference-Cited by-同舟云学术

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Determination of the absolute configuration at C-6 and C-7 of serricornin (4,6-dimethyl-7-hydroxy-3-nonanone), the sex pheromone of the cigarette beetle

Published:1981 Issue:12 Volume:22 Page:1127-1130
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Mori Kenji,Nomi (née Iwasawa) Hiroko,Chuman Tatsuji,Kohno Masahiro,Kato Kunio,Noguchi Masao

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. 4.6-dimethyl-7-hydroxy-nonan-3-one, a sex pheromone of the cigarette beetle (Lasioderma serricorne F.)

2. The Preparation of Four Optically Active Isomers of 3-Methylmalic Acid

3. Stereoselective synthesis of optically active forms of δ-multistriatin, the attractant for european populations of the smaller european elm bark beet

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1. The thiopyran route to polypropionates;Chemical Communications;2011

2. Synthesis of Pheromones;Chemical Synthesis of Hormones, Pheromones and Other Bioregulators;2010-08-13

3. The Synthesis of Insect Pheromones, 1979-1989;Total Synthesis of Natural Products;2007-02-20

4. Thiopyran Route to Polypropionates: An Efficient Synthesis of Serricornin;The Journal of Organic Chemistry;2006-10-14

5. Attractant pheromones of museum insect pests;AICCM Bulletin;2003-12

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