Selective acetolysis of 6-deoxy-sugar oligosaccharide building blocks governed by the armed–disarmed effect
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference38 articles.
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2. Armed/disarmed effects in glycosyl donors: rationalization and sidetracking
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1. A straightforward access to neohesperidose from naringin by acetolysis. Comparative behaviour of some flavonoid neohesperidosides and rutinosides under acetolysis;Tetrahedron;2014-02
2. Regioselective Acetolysis of HighlyO-Benzylated Carbohydrates Promoted by Iodine or an Iodine/Silane Combined Reagent: Use of Isopropenyl Acetate as an Alternative to Acetic Anhydride;European Journal of Organic Chemistry;2013-04-03
3. Analysis of carbohydrates and glycoconjugates by matrix-assisted laser desorption/ionization mass spectrometry: An update for 2007-2008;Mass Spectrometry Reviews;2011-08-17
4. The role of sugar configuration in the acetolysis of 6-deoxyhexose methyl glycosides;Carbohydrate Research;2009-11
5. Acetolysis of 6-Deoxysugar Disaccharide Building Blocks:exoversusendoActivation;European Journal of Organic Chemistry;2008-12
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