Literature DB >> 19048168

Chiral recognition of alpha-phenylethylamine by sucrose-based macrocyclic receptors.

Bartosz Lewandowski1, Slawomir Jarosz.   

Abstract

Simple chiral aza-crown ethers based on sucrose display high enantioselectivity in complexation of phenylethylammonium chlorides.

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Year:  2008        PMID： 19048168     DOI： 10.1039/b816476b

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


  5 in total

1.  Molecular recognition of organic ammonium ions in solution using synthetic receptors.

Authors:  Andreas Späth; Burkhard König
Journal:  Beilstein J Org Chem       Date:  2010-04-06       Impact factor: 2.883

2.  An efficient synthesis of novel sucrose-containing dilactams.

Authors:  Mykhaylo A Potopnyk; Sławomir Jarosz
Journal:  Monatsh Chem       Date:  2013-01-17       Impact factor: 1.451

3.  Fluorescent Molecular Cages with Sucrose and Cyclotriveratrylene Units for the Selective Recognition of Choline and Acetylcholine.

Authors:  Łukasz Szyszka; Marcin Górecki; Piotr Cmoch; Sławomir Jarosz
Journal:  J Org Chem       Date:  2021-03-12       Impact factor: 4.354

4.  Synthesis of a sucrose dimer with enone tether; a study on its functionalization.

Authors:  Zbigniew Pakulski; Norbert Gajda; Magdalena Jawiczuk; Jadwiga Frelek; Piotr Cmoch; Sławomir Jarosz
Journal:  Beilstein J Org Chem       Date:  2014-05-28       Impact factor: 2.883

5.  An efficient synthesis of a C12-higher sugar aminoalditol.

Authors:  Łukasz Szyszka; Anna Osuch-Kwiatkowska; Mykhaylo A Potopnyk; Sławomir Jarosz
Journal:  Beilstein J Org Chem       Date:  2017-10-16       Impact factor: 2.883
  5 in total

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