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Proline-threonine dipeptide as an organocatalyst for the direct asymmetric aldol reaction

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TETRAHEDRON-ASYMMETRY
卷 20, 期 15, 页码 1742-1745

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2009.06.018

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  1. CSIR, New Delhi

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A new proline-threonine (H-Pro-Thr-OH) dipeptide has been demonstrated as an efficient organocatalyst for a direct asymmetric aldol reaction. It was found that this new peptide-based catalyst efficiently catalyzed the reaction between an aldehyde and acetone to provide beta-hydroxy ketones in good yields with good enantioselectivities. (c) 2009 Elsevier Ltd. All rights reserved.

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