Stereochemical course of pheromone biosynthesis in the arctiid moth, Creatonotos transiens
- PMID: 6540200
- DOI: 10.1007/BF01949738
Stereochemical course of pheromone biosynthesis in the arctiid moth, Creatonotos transiens
Abstract
The biosynthetic conversion of a pyrrolizidine alkaloid (heliotrine, IV) to a male moth pheromone (hydroxydanaidal, III) is found to proceed with inversion of configuration at the remaining asymmetric center (C-7).
References
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- Science. 1969 Jun 6;164(3884):1170-2 - PubMed
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