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Expeditious oligosaccharide synthesis via selective, semi-orthogonal, and orthogonal activation onhogonall activation

Journal

CARBOHYDRATE RESEARCH
Volume 346, Issue 12, Pages 1371-1388

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.carres.2011.05.004

Keywords

Oligosaccharides; Selective activation; Strategy; Orthogonality; Glycosylation

Funding

  1. National Institute of General Medical Studies [GM077170]
  2. UM - St. Louis Graduate School

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Traditional strategies for oligosaccharide synthesis often require extensive protecting and/or leaving group manipulations between each glycosylation step, thereby increasing the total number of synthetic steps while decreasing the efficiency of the synthesis. In contrast, expeditious strategies allow for the rapid chemical synthesis of complex carbohydrates by minimizing extraneous chemical manipulations. Oligosaccharide synthesis by selective activation of one leaving group over another is one such expeditious strategy. Herein, the significant improvements that have recently emerged in the area of the selective activation are discussed. The development of orthogonal strategy further expands the scope of the selective activation methodology. Surveyed in this article, are representative examples wherein these excellent innovations have been applied to the synthesis of various oligosaccharide sequences. (C) 2011 Elsevier Ltd. All rights reserved.

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