Issue 2, 1992

Nonlinear relationship between the enantioselectivities for asymmetric reactions of monofunctional and bifunctional substrates. Synthesis of practically optically pure diols by the catalytic enantioselective diethylation of terephthalaldehyde

Abstract

An equation is presented which shows a nonlinear relationship between the enantioselectivities for asymmetric reactions of bifunctional and monofunctional substrates; practically complete enantioselectivity (100% e.e.) was observed in the enantioselective diethylation of terephthalaldehyde with diethylzinc using N,N-di(n- butyl) norephedrine and (S)-diphenyl(1-methylpyrrolidin-2-yl) methanol as chiral catalysts.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 106-108

Nonlinear relationship between the enantioselectivities for asymmetric reactions of monofunctional and bifunctional substrates. Synthesis of practically optically pure diols by the catalytic enantioselective diethylation of terephthalaldehyde

K. Soai, H. Hori and M. Kawahara, J. Chem. Soc., Chem. Commun., 1992, 106 DOI: 10.1039/C39920000106

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