Literature DB >> 21503344

Exclusive enantioselective recognition of glucopyranosides by inherently chiral hemicryptophanes.

Olivier Perraud1, Alexandre Martinez, Jean-Pierre Dutasta.   

Abstract

Inherently chiral hemicryptophanes were used to complex β- and α-glucoside derivatives with high diastereo- and enantio-selectivity. In most cases, the exclusive recognition by the M-hemicryptophane enantiomers was observed. © The Royal Society of Chemistry 2011

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Year:  2011        PMID： 21503344     DOI： 10.1039/c1cc10964b

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


  3 in total

1.  Counteranions at Peripheral Sites Tune Guest Affinity for a Protonated Hemicryptophane.

Authors:  Yannan Lin; Michael R Gau; Patrick J Carroll; Ivan J Dmochowski
Journal:  J Org Chem       Date:  2022-03-25       Impact factor: 4.198

2.  Enantioselective carbohydrate recognition by synthetic lectins in water.

Authors:  Pablo Ríos; Tiddo J Mooibroek; Tom S Carter; Christopher Williams; Miriam R Wilson; Matthew P Crump; Anthony P Davis
Journal:  Chem Sci       Date:  2017-03-30       Impact factor: 9.825

3.  Allosteric Recognition of Homomeric and Heteromeric Pairs of Monosaccharides by a Foldamer Capsule.

Authors:  Pedro Mateus; Nagula Chandramouli; Cameron D Mackereth; Brice Kauffmann; Yann Ferrand; Ivan Huc
Journal:  Angew Chem Int Ed Engl       Date:  2020-02-03       Impact factor: 15.336
  3 in total

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