A short efficient preparation of (+) and (-)-trans-2-phenylcyclohexanol

DOI: 10.1016/0957-4166(96)00409-0

Source and publish data:

Tetrahedron Asymmetry p. 3107 - 3108 (1996)

Update date:2022-08-16

Topics:

Authors:

Carpenter, Bryon E.

Hunt, Ian R.

Keay, Brian A.

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Article abstract of DOI:10.1016/0957-4166(96)00409-0

Both enantiomers of trans-2-phenylcyclohexanol (1) (Whitesell's auxiliary) have been prepared in a facile three step sequence starting from phenylmagnesium bromide and cyclohexene oxide using Lipase PS30 to facilitate the resolution of the racemic alcohol

Full text of DOI:10.1016/0957-4166(96)00409-0

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Product name:Cyclohexanol, 2-phenyl-, acetate, (1R,2S)-

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