A facile, one-step procedure for the conversion of 2-(trimethylsilyl) ethyl glycosides to their glycosyl chlorides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Synthetic Studies Toward Gangliosides and Their Analogs: Synthesis of Appropriately Protected Core Oligosaccharides as Construction Blocks
2. 2-(Trimethylsilyl)ethyl glycosides. 3. Synthesis, anomeric deblocking, and transformation into 1,2-trans 1-O-acyl sugars
3. Synthesis of a di-, tri-, and tetra-saccharide unit of the group B streptococcal common antigen
4. Thioglycosides were also unstable during di-n-butyltin oxide mediated benzylation reactions (unpublished results from this laboratory).
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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1. Mild method for the synthesis of α-glycosyl chlorides: A convenient protocol for quick one-pot glycosylation;Carbohydrate Research;2023-12
2. Synthesis of glycosyl chlorides using catalytic Appel conditions;Organic & Biomolecular Chemistry;2019
3. ChemInform Abstract: A Facile, One-Step Procedure for the Conversion of 2-(Trimethylsilyl) Ethyl Glycosides to Their Glycosyl Chlorides.;ChemInform;2010-08-23
4. Dichloromethyl Methyl Ether;Encyclopedia of Reagents for Organic Synthesis;2005-10-15
5. Dichloromethyl Methyl Ether;Encyclopedia of Reagents for Organic Synthesis;2005-10-15
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