CHIRALITY AND INSECT PHEROMONES
作者： Kenji Mori
DOI: 10.1002/(SICI)1520-636X(1998)10:7<578::AID-CHIR5>3.0.CO;2-Z
关键词:
摘要: Enantioselective synthesis is a central component of research on the effect chirality relationships between pheromone structure and bioactivity. The syntheses stegobinone, drugstore beetle pheromone, frontalin, bark are reported as examples stereocontrolled synthesis. Chirality governs biodiversity perception, illustrated by discussion absolute configuration activity. 10:578–586, 1998. © 1998 Wiley-Liss, Inc.
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