首页> 外文期刊>Journal of Fluorine Chemistry >Highly enantioselective synthesis of dihydroquinazolinones through Sc(OTf)(3)-catalyzed intramolecular amidation of imines
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Highly enantioselective synthesis of dihydroquinazolinones through Sc(OTf)(3)-catalyzed intramolecular amidation of imines

机译:通过Sc(OTf)(3)催化的亚胺分子内酰胺化对二氢喹唑啉酮的高度对映选择性合成

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摘要

A Sc(OTf)(3)-catalyzed intramolecular amidation of imines with a novel fluorous bis(oxazolines) as ligand is presented. The corresponding chiral dihydroquinazolinones were obtained in 76-94% yield with enantioselectivities up to 98%. The fluorous ligand can be easily recovered and reused at least three times without significant loss of enantioselectivity. (C) 2014 Elsevier B.V. All rights reserved.
机译:提出了一种Sc(OTf)(3)催化的亚胺分子内酰胺化反应,该反应以新型氟双(恶唑啉)作为配体。以76-94%的收率获得相应的手性二氢喹唑啉酮,对映选择性高达98%。氟配体可以容易地回收并重复使用至少三遍,而对映选择性没有明显损失。 (C)2014 Elsevier B.V.保留所有权利。

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