REGIOSELECTIVE RING CLEAVAGE OF OXIRANES CATALYZED BY ORGANOTIN HALIDE - TRIPHENYLPHOSPHINE COMPLEX

DOI: 10.1016/S0040-4039(00)84706-1

Source and publish data:

Tetrahedron Letters p. 3021 - 3024 (1986)

Update date:2022-08-05

Topics:

Authors:

Shibata, Ikuya

Baba, Akio

Matsuda, Haruo

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Article abstract of DOI:10.1016/S0040-4039(00)84706-1

Vicinal chloroesters are formed in high yield from the reaction of oxiranes and benzoyl chloride in the presence of organotin halide - triphenylphosphine complex with enhanced regioselectivity in oxirane ring cleavage.

Full text of DOI:10.1016/S0040-4039(00)84706-1

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