Literature DB >> 17616144

Design of a novel inherently chiral calix[4]arene for chiral molecular recognition.

Seiji Shirakawa1, Akihiro Moriyama, Shoichi Shimizu.   

Abstract

A newly designed inherently chiral calix[4]arene was synthesized and resolved to an optically pure form. Enantiomeric recognition ability of the chiral calix[4]arene was examined using 1H NMR experiments with mandelic acid. In addition, the chiral calix[4]arene was applied to asymmetric reactions, as an organocatalyst.

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Year:  2007        PMID： 17616144     DOI： 10.1021/ol071249p

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


  4 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.  An easy assembled fluorescent sensor for dicarboxylates and acidic amino acids.

Authors:  Xiao-Bo Zhou; Yuk-Wang Yip; Wing-Hong Chan; Albert W M Lee
Journal:  Beilstein J Org Chem       Date:  2011-01-17       Impact factor: 2.883

3.  Inherently chiral calix[4]arenes via oxazoline directed ortholithiation: synthesis and probe of chiral space.

Authors:  Simon A Herbert; Laura J van Laeren; Dominic C Castell; Gareth E Arnott
Journal:  Beilstein J Org Chem       Date:  2014-11-25       Impact factor: 2.883

4.  Qualitative analysis of the helical electronic energy of inherently chiral calix[4]arenes: an approach to effectively assign their absolute configuration.

Authors:  Shuang Zheng; Ming-Liang Chang; Jing Zhou; Jing-Wei Fu; Qing-Wei Zhang; Shao-Yong Li; Wei Qiao; Jun-Min Liu
Journal:  Int J Mol Sci       Date:  2014-06-03       Impact factor: 5.923
  4 in total

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