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Chirality and field activity of rhynchophorol, the aggregation pheromone of the American palm weevil

✍ Scribed by A. C. Oehlschlager; H. D. Pierce; B. Morgan; P. D. C. Wimalaratne; K. N. Slessor; G. G. S. King; G. Gries; R. Gries; J. H. Borden; L. F. Jiron; C. M. Chinchilla; R. G. Mexzan

Publisher
Springer
Year
1992
Tongue
English
Weight
172 KB
Volume
79
Category
Article
ISSN
0028-1042

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πŸ“œ SIMILAR VOLUMES

Pheromone Synthesis, CXLV. Synthesis of
Pheromone Synthesis, CXLV. Synthesis of the Enantiomers of Rhynchophorol [(E)-6-Methyl-2-hepten-4-ol], the Male-Produced Aggregation Pheromone of the American Palm Weevil,Rhynchophorus palmarum
✍ Mori, Kenji ;Ishigami, Ken πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 437 KB

## Abstract Both the enantiomers of rhynchophorol [(__E__)‐6‐methyl‐2‐hepten‐4‐ol (1)], the male‐produced aggregation pheromone of the American palm weevil (__Rhynchophorus palmarum__), have been synthesized by reducing their precursors, (__R__)‐ and (__S__)‐6‐methyl‐2‐heptyn‐4‐ol (2), which have b