A highly stereoselective synthesis of (E)-1-substituted-1,3-dienes |
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Authors: | R. Block J. Abecassis |
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Affiliation: | Laboratoire des Carbocycles, ERA 316, Université de Paris-Sud Bâtiment 420, 91405 Orsay, France |
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Abstract: | (E)-1-substituted-1,3-dienes are obtained with high stereoselectivity by the thermal extrusion of SO2 from 2-substituted-2,5-dihydrothiophene-1,1-dioxides generated by a retro Diels-Alder reaction. An application to the synthesis of (E)-9,11-dodecadien- 1-yl acetate, a sex pheromone of the red-bollworm moth is described. |
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