Issue 12, 1992

A novel coenzyme NAD(P)+–NAD(P)H model with axial chirality. Its preparation and stereoselectivity

Abstract

An axially chiral NAD(P)H model 1 bearing a 2′-methoxy-1′-naphthyl group at the C-2 position is prepared; the reduction of methyl benzoylformate with the optically active model, (+)- or (–)-1, in the presence of magnesium ion gives (R)- or (S)-isomer of methyl mandelate, respectively, in over 95% enantiomeric excess.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 905-906

A novel coenzyme NAD(P)+–NAD(P)H model with axial chirality. Its preparation and stereoselectivity

M. Fujii, T. Kamata, M. Okamura and A. Ohno, J. Chem. Soc., Chem. Commun., 1992, 905 DOI: 10.1039/C39920000905

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