Literature DB >> 12240329

Novel chiral imidazole cyclophane receptors: synthesis and enantioselective recognition for amino acid derivatives.

J S You1, X Q Yu, G L Zhang, Q X Xiang, J B Lan, R G Xie.   

Abstract

Novel chiral imidazole cyclophane receptors were synthesized by highly selective N-alkylation of the imadazolyl 1N-position of the bridged histidine diester 2 with the dibromide in the presence of NaH; these receptors exhibit good chiral recognition toward the enantiomers of L- and D-amino acid derivatives (up to KD/KL = 3.52, delta delta G0 = -3.11 kJ mol-1) in CHCl3 at 25.0 degrees C.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 12240329     DOI: 10.1039/b103325p

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Facile synthesis of optically active imidazole derivatives.

Authors:  Ales Marek; Jiri Kulhanek; Miroslav Ludwig; Filip Bures
Journal:  Molecules       Date:  2007-05-30       Impact factor: 4.411

2.  Synthesis and chiral recognition properties of novel fluorescent chemosensors for amino acid.

Authors:  Xiao-Huan Huang; Yong-Bing He; Chen-Guang Hu; Zhi-Hong Chen
Journal:  J Fluoresc       Date:  2008-06-12       Impact factor: 2.217

3.  (S)-2-(1H-Imidazol-1-yl)-3-phenyl-propanol.

Authors:  Zuxing Yang; Siping Wei; Wenhai Wang; Hua Chen; Jingbo Lan
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-02-27
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.