Efficient routes to cyclic 2,3-epoxyalcohols from cycloalkenyl ketones, via cycloalkenyl alcohols

DOI: 10.1016/S0040-4020(01)80560-3

Source and publish data:

Tetrahedron p. 10317 - 10338 (1993)

Update date:2022-08-02

Topics:

Authors:

Marson Marson

Walker Walker

Pickering

Harper Harper

Wrigglesworth

Edge Edge

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Article abstract of DOI:10.1016/S0040-4020(01)80560-3

The minimising of torsional strain and non-bonding interactions is proposed as the explanation of high diastereoselectivity observed in the epoxidation of cycloalkenyl alcohols, reported for twenty three examples. The resulting 2,3-epoxyalcohols are key i

Full text of DOI:10.1016/S0040-4020(01)80560-3

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