A 2-silylethanol-based anomeric linker for carbohydrates; transformation into 1-O-acyl derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. Combinatorial synthesis — the design of compound libraries and their application to drug discovery
2. Organic Chemistry on Solid Supports
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4. 2-(Trimethylsilyl)Ethyl(TMSEt) Glycosides; Anomeric Blocking, Deblocking and Activation in the Synthesis of Oligosaccharides.
5. Boron trifluoride etherate as an effective reagent for the stereoselective one-pot conversion of acetylated 2-trimethylsilylethyl glycosides into sugar 1,2-trans-acetates
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2. Janus glycosides of next generation: Synthesis of 4-(3-chloropropoxy)phenyl and 4-(3-azidopropoxy)phenyl glycosides;Carbohydrate Research;2019-01
3. Application of a Janus aglycon with dual function in benzyl-free synthesis of spacer-armed oligosaccharide fragments of polysaccharides from rhizobacterium Azospirillum brasilense sp7;Carbohydrate Research;2018-07
4. 1-Methyl 1′-cyclopropylmethyl (MCPM) as an anomeric protecting group;Tetrahedron;2011-08
5. ChemInform Abstract: A 2-Silylethanol-Based Anomeric Linker for Carbohydrates; Transformation into 1-O-Acyl Derivatives.;ChemInform;2010-08-03
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