Direct asymmetric aldol reactions catalyzed by l-proline-2,4,6-trinitroanilide |
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Authors: | Kosuke Sato Rumiko Shimazawa Kiyomi Kakiuchi |
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Affiliation: | a Graduate School of Materials Science, Nara Institute of Science and Technology (NAIST), Nara 630-0192, Japan b Faculty of Pharmaceutical Sciences, Doshisha Women’s College of Liberal Arts, Kyoto 610-0395, Japan |
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Abstract: | Direct aldol reactions of several aromatic aldehydes with ketones using l-proline-2,4,6-trinitroanilide catalyst 2d were conducted. Under optimized conditions, high enantioselectivity (99% ee), regioselectivity (up to 95:5), and diastereoselectivity (up to 98:2) were achieved. |
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