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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Asymmetric α-allylation of α-branched aldehydes with allyl alcohols by synergistic catalysis using an achiral palladium complex and a chiral primary amino acid
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Asymmetric α-allylation of α-branched aldehydes with allyl alcohols by synergistic catalysis using an achiral palladium complex and a chiral primary amino acid

机译:通过使用甲状腺钯络合物和手性原发性氨基酸通过协同催化催化催化与烯丙基醇的不对称α-烯丙基α-烯丙基

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摘要

Highly enantioselective direct α-allylation of α-branched aldehydes with simple allyl alcohols was achieved by the combined use of an achiral transition-metal catalysis with a palladium complex and a chiral organocatalysis with a readily obtainable primary α-amino acid. Various α-allylated aldehydes possessing a stereocontrolled quaternary carbon stereogenic center were synthesized in high yields with high enantioselectivity.
机译:通过将钯络合物和易于获得的初级α-氨基酸的手性有机能相应使用甲状腺过渡金属催化,实现了具有简单烯丙基醇的α-支链醛的高映选择性直接α-烯丙基化。 具有高收率的具有高收率的各种α-烯丙基醛醛以高映的浓缩性合成。

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