Literature DB >> 16494458

Crown ethers as building blocks for carbohydrate receptors.

Monika Mazik1, Matthias Kuschel, Willi Sicking.   

Abstract

Acyclic receptors containing neutral hydrogen bonding sites, such as amino-pyridine groups and a crown unit, perform effective recognition of neutral sugar molecules through multiple interactions. Receptor 1 has been shown to be a particularly effective and highly selective receptor for beta-glucopyranoside.

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Year:  2006        PMID： 16494458     DOI： 10.1021/ol052902g

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


  4 in total

1.  DFT modeling on the suitable crown ether architecture for complexation with Cs⁺ and Sr²⁺ metal ions.

Authors:  Anil Boda; Sk Musharaf Ali; Madhav R K Shenoi; Hanmanth Rao; Sandip K Ghosh
Journal:  J Mol Model       Date:  2010-07-30       Impact factor: 1.810

2.  Regiochemical Effects on the Carbohydrate Binding and Selectivity of Flexible Synthetic Carbohydrate Receptors with Indole and Quinoline Heterocyclic Groups.

Authors:  Khushabu Thakur; Milan A Shlain; Mateusz Marianski; Adam B Braunschweig
Journal:  European J Org Chem       Date:  2021-09-12

Review 3.  Carbohydrate recognition by boronolectins, small molecules, and lectins.

Authors:  Shan Jin; Yunfeng Cheng; Suazette Reid; Minyong Li; Binghe Wang
Journal:  Med Res Rev       Date:  2010-03       Impact factor: 12.944

4.  Recognition properties of receptors consisting of imidazole and indole recognition units towards carbohydrates.

Authors:  Monika Mazik; André Hartmann
Journal:  Beilstein J Org Chem       Date:  2010-02-02       Impact factor: 2.883
  4 in total

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