Literature DB >> 15797140

Synthesis of regioselectively and uniformly modified maltoheptaose derivatives from cyclomaltoheptaose precursors.

David Lesur1, Abdoulaye Gassama, Vincent Moreau, Serge Pilard, Florence Djedaïni-Pilard.   

Abstract

Heptadeoxy-6(I-VII)-halo, -azido, and hepta-6(I-VII)S-hepta(N-Boc-2-amino)ethyl-6(I-VII)-heptathiomaltoheptaose derivatives were prepared by acetolysis of the corresponding per-C-6-modified beta-cyclodextrin derivatives. The rapid and convenient structural characterisation of all of the modified oligosaccharides by ESIMS is described.

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Year:  2005        PMID: 15797140     DOI: 10.1016/j.carres.2005.01.021

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  1 in total

1.  One-Pot Synthesis of Asymmetrically Difunctionalized Oligomaltosides by Cyclodextrin Ring Opening.

Authors:  Matthieu Pélingre; Meriem Smadhi; Abed Bil; Véronique Bonnet; José Kovensky
Journal:  ChemistryOpen       Date:  2021-04       Impact factor: 2.911

  1 in total

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