Lipase mediated treatment of racemic 2-(hydroxymethyl)cyclohexanone, (+/-)-1, with vinyl acetate allows enantioselective acetylation to give the acetate (R)-(+)-4 and unreacted (S)-(+)-1 in satisfactory yield and enantiomeric purity. The absolute configuration of (S)-(+)-1 (and therefore that of (R)-(+)-4 as well) was determined by the analysis of the n-->pi* Cotton effect at 290 nm present in the CD spectrum of (S)-(+)-1 by means of the octant rule and CNDO/S calculations. Furthermore the optical rotatory power of optically pure (S)-(+)-1 and (R)-(+)-4 have been determined.

Enzymatic preparation and absolute configuration of (+)-2-(hydroxymethyl)cyclohexanone

CATELANI, GIORGIO;
1998-01-01

Abstract

Lipase mediated treatment of racemic 2-(hydroxymethyl)cyclohexanone, (+/-)-1, with vinyl acetate allows enantioselective acetylation to give the acetate (R)-(+)-4 and unreacted (S)-(+)-1 in satisfactory yield and enantiomeric purity. The absolute configuration of (S)-(+)-1 (and therefore that of (R)-(+)-4 as well) was determined by the analysis of the n-->pi* Cotton effect at 290 nm present in the CD spectrum of (S)-(+)-1 by means of the octant rule and CNDO/S calculations. Furthermore the optical rotatory power of optically pure (S)-(+)-1 and (R)-(+)-4 have been determined.
1998
Barili, Pl; Catelani, Giorgio; Giorgi, R.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/50730
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