The catalytic activities of 3-decyl-beta-proline in Michael addition using water as the solvent were investigated, showing that the decyl substituent promoted the reaction through hydrophobic interactions to afford high yield and high diastereoselectivity under low catalyst loading.
3-Decyl-beta-proline, which has a highly lipophilic substituent, was synthesized, and its catalytic activities in Michael addition using water as the solvent were investigated. The decyl substituent promoted the reaction by hydrophobic interactions to afford the Michael adduct in a high yield and with high diastereoselectivity under low catalyst loading.
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