4.6 Article

Highly diastereo- and enantioselective organocatalytic addition of acetone to beta-substituted alpha-ketoesters via dynamic kinetic resolution

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ORGANIC & BIOMOLECULAR CHEMISTRY
卷 7, 期 10, 页码 2208-2213

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ROYAL SOC CHEMISTRY
DOI: 10.1039/b822127h

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  1. The Key Laboratory of Organic Synthesis of Jiangsu Province

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L-Proline catalyzes the aldol addition reaction of acetone to beta-substituted alpha-ketoesters with dynamic kinetic resolution, providing the desired adduct in good yield with excellent diastereoselectivity ( up to >99:1 dr) and enantioselectivity (up to 98% ee). The absolute configuration of the chiral adduct was assigned by single-crystal X-ray diffraction analysis. A tentative explanation of the stereochemical outcome is proposed.

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