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Issue 2, 1993
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β-Hydroxy sulfoximines as catalysts for the enantioselective alkylation of aldehydes

Abstract

Optically active β-hydroxy sulfoximines are catalysts for the enantioselective ethyl transfer from diethylzinc to aldehydes affording secondary alcohols with high enantioselectivity; the structure of a dimeric zinc alkoxide has been determined by X-ray diffraction analysis.

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Article type: Paper
DOI: 10.1039/C39930000182
Citation: J. Chem. Soc., Chem. Commun., 1993, 182-183
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    β-Hydroxy sulfoximines as catalysts for the enantioselective alkylation of aldehydes

    C. Bolm, J. Müller, G. Schlingloff, M. Zehnder and M. Neuburger, J. Chem. Soc., Chem. Commun., 1993, 182
    DOI: 10.1039/C39930000182

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