Literature DB >> 22751352

Controlled synthesis and alkaline earth ion binding of switchable formamidoxime-based crown ether analogs.

Yi Yan1, Weiwen Zhao, Ganga Viswanathan Bhagavathy, Alexandre Faurie, Nicholas J Mosey, Anne Petitjean.   

Abstract

The partial positive charge of amide protons is used to promote macrocyclization and form crown-ether analogs. Their deprotonation generates very selective pH-switchable alkaline earth ion receptors only in the presence of an appropriate substrate.

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Year:  2012        PMID: 22751352     DOI: 10.1039/c2cc33090c

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


  2 in total

1.  Spectroscopic, DFT, and XRD Studies of Hydrogen Bonds in N-Unsubstituted 2-Aminobenzamides.

Authors:  Malose Jack Mphahlele; Marole Maria Maluleka; Lydia Rhyman; Ponnadurai Ramasami; Richard Mokome Mampa
Journal:  Molecules       Date:  2017-01-04       Impact factor: 4.411

2.  N,N'-[2,2'-(Phenyl-aza-nedi-yl)bis-(ethane-2,1-di-yl)]dipicolinamide.

Authors:  Gao-Nan Li; Zhi-Gang Niu; Mei-Qi Huang; Ying Zou; Liang-Jiang Hu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2013-04-10
  2 in total

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