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Digitale Medien

Chirality and insect pheromones (1998)

Mori, Kenji

New York, NY [u.a.] : Wiley-Blackwell

Chirality 10 (1998), S. 578-586

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Details

ISSN: 0899-0042

Schlagwort(e): bark beetle pheromone ; drugstore beetle pheromone ; enantioselective synthesis ; frontalin ; stegobinone ; stereochemistry-pheromone activity relationships ; Chemistry ; Organic Chemistry

Quelle: Wiley InterScience Backfile Collection 1832-2000

Thema: Chemie und Pharmazie

Notizen: Enantioselective synthesis is a central component of research on the effect of chirality on the relationships between pheromone structure and pheromone bioactivity. The syntheses of stegobinone, the drugstore beetle pheromone, and frontalin, a bark beetle pheromone, are reported as examples of stereocontrolled synthesis. Chirality governs the biodiversity of pheromone perception, as illustrated by the discussion on the relationships between absolute configuration and pheromone activity. Chirality 10:578-586, 1998. © 1998 Wiley-Liss, Inc.

Zusätzliches Material: 5 Ill.

Materialart: Digitale Medien

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