21. A Journey into Recent Microwave-Assisted Carbohydrate Chemistry

  1. Prof. Antonio de la Hoz3 and
  2. Dr. André Loupy4
  1. Antonino Corsaro1,
  2. Venerando Pistarà1,
  3. Maria Assunta Chiacchio1 and
  4. Giovanni Romeo2

Published Online: 27 FEB 2013

DOI: 10.1002/9783527651313.ch21

Microwaves in Organic Synthesis, Volume 1, Third Edition

Microwaves in Organic Synthesis, Volume 1, Third Edition

How to Cite

Corsaro, A., Pistarà, V., Chiacchio, M. A. and Romeo, G. (2012) A Journey into Recent Microwave-Assisted Carbohydrate Chemistry, in Microwaves in Organic Synthesis, Volume 1, Third Edition (eds A. de la Hoz and A. Loupy), Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany. doi: 10.1002/9783527651313.ch21

Editor Information

  1. 3

    Universidad de Castilla-La Mancha, Facultad de Ciencias y, Technologías Químicas, Avda. Camilo Josè Cela 10, 13071 Ciudad Real, Spain

  2. 4

    Universitè Paris-Sud 11, Laboratoire des Réactions, Sélectives sur Supports, Laboratoire de Chimie des, procédés et Substances Naturelles, ICMMO, Bâtiment 410, 91405 Orsay, France

Author Information

  1. 1

    Università, di Catania, Dipartimento di Scienze del, Farmaco, Viale A. Doria 6, 95125 Catania, Italy

  2. 2

    Università di Messina, Dipartimento Farmaco-Chimico, Viale SS. Annunziata 6, 98168 Messina, Italy

Publication History

  1. Published Online: 27 FEB 2013
  2. Published Print: 5 DEC 2012

ISBN Information

Print ISBN: 9783527331161

Online ISBN: 9783527651313

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Keywords:

  • carbohydrates;
  • microwave-assisted chemistry;
  • acylation;
  • glycosylation;
  • halogenation;
  • anomerization;
  • sugar derivatives;
  • heterocycles;
  • nanostructures

Summary

This chapter on recent microwave-assisted carbohydrate chemistry updates our chapter in the previous edition, and covers the period from 2006 until today. The topics presented here are acylations, glycosylations, halogenations-dehalogenations, sulfations, and anomerizations; several syntheses are reported relating to sugar derivatives, including biologically and pharmacologically active derivatives, and then syntheses of heterocycles, sugar phosphorus compounds, and nanostructured materials.