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首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >Highly enantioselective synthesis of chiral allylic alcohols by asymmetric addition of novel mixed reagents of trialkenylbismuthines/dialkylzincs to aldehydes
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Highly enantioselective synthesis of chiral allylic alcohols by asymmetric addition of novel mixed reagents of trialkenylbismuthines/dialkylzincs to aldehydes

机译:通过不对称地将三烯基双变异蛋白/二烷基锌的新型混合试剂不对称添加到醛中,高度手性地合成手性烯丙基醇

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摘要

A novel mixture of reagents of trialkenylbismuthines/dialkylzines was developed and applied toward the synthesis of chiral allylic alcohols. The chiral beta-amino alcohols catalyzed addition of the mixed reagents of trialkenylbismuthines/dialkylzincs to aldehydes gave enantiomerically enriched allylic alcohols with up to 97% ee. (c) 2007 Elsevier Ltd. All rights reserved.
机译:开发了一种新的三烯基双突变体/二烷基zines试剂混合物,并将其用于手性烯丙基醇的合成。手性β-氨基醇催化将三烯基双突变蛋白/二烷基锌的混合试剂加成到醛中,得到对映体富集的烯丙醇,其ee高达97%。 (c)2007 Elsevier Ltd.保留所有权利。

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