A stereospecific route to functionalized alkenes from tetrahydrofurfurylic acetates, synthesis of pheromones
R Amouroux, S Ejjiyar
Index: Amouroux, Roger; Ejjiyar, Soumeya Tetrahedron Letters, 1991 , vol. 32, # 26 p. 3059 - 3062
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Citation Number: 11
Abstract
Abstract Pure Z or E γ-iodoalkenes were prepared by a ring opening-elimination tandem reaction of erythro or threo secondary tetrahydrofurfurylic acetates with Me 3 SiCl/NaI. Applications to the synthesis of pheromones of Musca domestica and of Orgyia pseudotsugata are reported.
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