Enantioselective synthesis of (1R,2R)- and (1S,2S)-2-nitroxycyclohexan-1-ols

DOI: 10.1016/0957-4166(95)00409-2

Source and publish data:

Tetrahedron Asymmetry p. 13 - 16 (1996)

Update date:2022-08-05

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Authors:

Basavaiah, Deevi

Pandiaraju, Subramanian

Muthukumaran, Kannan

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Article abstract of DOI:10.1016/0957-4166(95)00409-2

A simple and convenient methodology has been developed for the synthesis of (1R,2S)-2-nitroxycyclohexan-1-ols in enantiomerically pure form via pig liver acetone powder (PLAP) mediated hydrolysis of racemic trans-1-acetoxy-2-nitroxycyclohexane.

Full text of DOI:10.1016/0957-4166(95)00409-2

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Product name:(+)-trans-1-acetoxy-2-nitroxycyclohexane

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