Steric control of the epoxidation of 1-hydroxymethyl-3-cyclopentene using aryl or silyl hydroxyl protecting groups

DOI: 10.1016/S0040-4039(00)61128-0

Source and publish data:

Tetrahedron Letters p. 5503 - 5504 (1992)

Update date:2022-08-03

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Authors:

Agrofoglio

Condom Condom

Guedj Guedj

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Article abstract of DOI:10.1016/S0040-4039(00)61128-0

A good anti-stereoselectivity is observed in the epoxidation of 1-hydroxymethyl-3-cyclopentene using tert-butyldimethylsilyl chloride as an hydroxyl protecting group (ratio anti:syn 8.2:1).

Full text of DOI:10.1016/S0040-4039(00)61128-0

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