首页> 外文期刊>Letters in organic chemistry >Enantioselective michael addition of malonates to aromatic α,β-unsaturated aldehydes organocatalyzed by (s)-2-[bis(3,4,5- trifluorophenyl) trimethylsilanyloxymethyl]pyrrolidine
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Enantioselective michael addition of malonates to aromatic α,β-unsaturated aldehydes organocatalyzed by (s)-2-[bis(3,4,5- trifluorophenyl) trimethylsilanyloxymethyl]pyrrolidine

机译:(s)-2- [双(3,4,5-三氟苯基)三甲基甲硅烷基氧甲基]吡咯烷酮有机催化的丙二酸酯向芳香族α,β-不饱和醛的对映选择性迈克尔加成反应

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摘要

The Michael addition of malonates to aromatic α,β-unsaturated aldehydes was efficiently organocatalyzed by (S)-2-[bis(3,4,5-trifluorophenyl) trimethylsilanyoxymethyl]pyrrolidine, derived from L-proline to afford the corresponding adducts in good yields with good to excellent enantioselectivities.
机译:丙二酸酯向芳族α,β-不饱和醛的迈克尔加成反应是由(L)脯氨酸衍生的(S)-2- [双(3,4,5-三氟苯基)三甲基硅酰氧基甲基]吡咯烷有效地有机催化的,以得到良好的相应加合物产生具有良好或优异的对映选择性的化合物。

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