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Zn-Proline catalyzed direct aldol reaction in aqueous media

Zn-Proline catalyzed direct aldol reaction in aqueous media Zn complexes of proline, lysine and arginine are efficient catalysts for the aldol addition of p-nitrobenzaldehyde and acetone in aqueous medium, giving quantitative yields and enantiomeric excesses up to 56% with 5 mol% of the catalysts at room temperature. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Chemical Communications Royal Society of Chemistry

Zn-Proline catalyzed direct aldol reaction in aqueous media

Royal Society of Chemistry — Apr 16, 2003

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Royal Society of Chemistry
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Abstract

Zn complexes of proline, lysine and arginine are efficient catalysts for the aldol addition of p-nitrobenzaldehyde and acetone in aqueous medium, giving quantitative yields and enantiomeric excesses up to 56% with 5 mol% of the catalysts at room temperature.

Journal

Chemical CommunicationsRoyal Society of Chemistry

Published: Apr 16, 2003

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