首页> 外文期刊>Chemical Communications >Asymmetric Synthesis Of Either Diastereomer Of Trifluoromethylated Allylic Amines By The Selective Reduction Of Trifluoromethyl α,β-unsaturated N-tert-butanesulfinyl Ketoimines
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Asymmetric Synthesis Of Either Diastereomer Of Trifluoromethylated Allylic Amines By The Selective Reduction Of Trifluoromethyl α,β-unsaturated N-tert-butanesulfinyl Ketoimines

机译:通过选择性还原三氟甲基α,β-不饱和N-叔丁亚磺酰基酮亚胺的不对称合成三氟甲基化烯丙胺的非对映异构体

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摘要

Regio- and diastereoselective reduction of chiral trifluoromethyl α, β-unsaturated N-tert-butanesulfinyl ketoimines 1 was achieved by choosing appropriate reducing agent and either diastereomer of the corresponding trifluoromethylated allylic amines was obtained with good yield and excellent diastereoselectivityrn(up to >99 : 1 dr).
机译:通过选择合适的还原剂可以实现手性三氟​​甲基α,β-不饱和N-叔丁烷亚磺酰基酮亚胺1的区域和非对映选择性还原,并且相应的三氟甲基化烯丙基胺的非对映异构体均具有良好的收率和优异的非对映选择性rn(高达> 99: 1博士)。

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