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首页> 外文期刊>Chirality: The pharmacological, biological, and chemical consequences of molecular asymmetry >Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by Chiral O,N,O-tridentate Phenol Ligands Derived From Camphor
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Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by Chiral O,N,O-tridentate Phenol Ligands Derived From Camphor

机译:樟脑衍生的手性O,N,O-三齿苯酚配体催化二乙基锌对醛的对映选择性加成

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摘要

Chiral O,N,O-tridentate phenol ligands bearing a camphor backbone were found to be effective chiral catalysts for the enantioselective addition of diethylzinc to aromatic aldehydes, resulting in high enantioselectivities (80-95% ee) at room temperature. (C) 2015 Wiley Periodicals, Inc.
机译:发现带有樟脑主链的手性O,N,O-三齿酚配体是将二乙基锌对映选择性加成到芳族醛中的有效手性催化剂,在室温下产生高对映选择性(80-95%ee)。 (C)2015年Wiley Periodicals,Inc.

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