Literature DB >> 15070294

Exceptional chiral recognition of racemic carboxylic acids by calix[4]arenes bearing optically pure alpha,beta-amino alcohol groups.

Yan-Song Zheng1, Chun Zhang.   

Abstract

Calixarenes bearing optically pure alpha,beta-amino alcohol groups at their lower rim exhibit exceptional and efficient chiral recognition ability in discrimination of racemic mandelic acid, 2,3-dibenzoyltartaric acid and 2-hydroxy-3-methylbutyric acid. [structure: see text]

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Year:  2004        PMID: 15070294     DOI: 10.1021/ol036122o

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Inherently chiral calixarenes: synthesis, optical resolution, chiral recognition and asymmetric catalysis.

Authors:  Shao-Yong Li; Yao-Wei Xu; Jun-Min Liu; Cheng-Yong Su
Journal:  Int J Mol Sci       Date:  2011-01-17       Impact factor: 5.923

2.  Comparison of Binding Affinities of Water-Soluble Calixarenes with the Organophosphorus Nerve Agent Soman (GD) and Commonly-Used Nerve Agent Simulants.

Authors:  Jayne A Ede; Peter J Cragg; Mark R Sambrook
Journal:  Molecules       Date:  2018-01-19       Impact factor: 4.411

  2 in total

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