A stereospecific route to functionalized alkenes from tetrahydrofurfurylic acetates, synthesis of pheromones

DOI: 10.1016/0040-4039(91)80688-3

Source and publish data:

Tetrahedron Letters p. 3059 - 3062 (1991)

Update date:2022-08-10

Topics:

Authors:

Amouroux, Roger

Ejjiyar, Soumeya

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Article abstract of DOI:10.1016/0040-4039(91)80688-3

Pure Z or E γ-iodoalkenes were prepared by a ring opening-elimination tandem reaction of erythro or threo secondary tetrahydrofurfurylic acetates with Me₃SiCl/NaI. Applications to the synthesis of pheromones of Musca domestica and of Orgyia pseudotsugata are reported.

Full text of DOI:10.1016/0040-4039(91)80688-3

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