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手性叔氨基萘酚配体对不对称苯甲酰化芳香醛转移的结构影响。

Structural influence of chiral tertiary aminonaphthol ligands on the asymmetric phenyl transfer to aromatic aldehydes.

机构信息

School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou, China.

出版信息

Chirality. 2011 Mar;23(3):222-7. doi: 10.1002/chir.20903. Epub 2010 Sep 29.

Abstract

A series of chiral tertiary aminonaphthol ligands were prepared from 2-naphthol, (S)-1-phenylethylamine, and aldehydes with diverse substituted groups. The results of asymmetric phenyl transfer to aromatic aldehydes catalyzed by these chiral ligands indicated that enantioselectivities were greatly influenced by the electronic and steric effects of the ligands.

摘要

一系列手性叔氨基萘酚配体是由 2-萘酚、(S)-1-苯乙胺和带有各种取代基的醛制备的。这些手性配体催化不对称苯转移到芳香醛的结果表明,配体的电子和空间效应极大地影响了对映选择性。

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