188709-32-2Relevant articles and documents
Enantioselective synthesis of haminol-1, an alarm pheromone of a Mediterranean mollusc
Solladie, Guy,Somny, Frederic,Colobert, Francoise
, p. 801 - 810 (2007/10/03)
The first enantioselective synthesis of (-)-(R)-haminol-1 is described in this paper. The chiral part of the molecule was prepared by reduction of an optically active β-ketosulfoxide. The all-trans trienic part was stereoselectively synthesized via reductive elimination of a 1,6-dibenzoate-2,4-diene with sodium amalgam.