Aza-Wittig reaction of sugar isothiocyanates and sugar iminophosphoranes: An easy entry to unsymmetrical sugar carbodiimides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Carbodiimide chemistry: recent advances
2. Tetrabutylammonium Fluoride Promoted Intramolecular Nucleophilic Attack of an Ester Group on a Carbodiimide: Preparation of 1,3-Oxazolin-5-ones and 3,1-Benzoxazin-4-ones
3. Iminophosphoranes: Useful Building Blocks for the Preparation of Nitrogen-Containing Heterocycles
4. A new route to cyclic urea derivatives of sugars via phosphinimines
5. Glycosylazide als Ausgangsbasis zur Gewinnung von Nucleosidanalogen, 2. Synthese von Tetrazol-Nucleosiden
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1. Investigations of Scope and Mechanism of Nickel-Catalyzed Transformations of Glycosyl Trichloroacetimidates to Glycosyl Trichloroacetamides and Subsequent, Atom-Economical, One-Step Conversion to α-Urea-Glycosides;Chemistry - A European Journal;2014-06-06
2. Recent developments in glycosyl urea synthesis;Carbohydrate Research;2014-02
3. A convenient synthesis of N-linked diglycose derivatives based on one-pot tandem Staudinger/aza-Wittig/reduction and biological evaluation;Carbohydrate Research;2013-05
4. Synthesis and glycosidase inhibitory activity of isourea-type bicyclic sp2-iminosugars related to galactonojirimycin and allonojirimycin;Tetrahedron;2012-01
5. ChemInform Abstract: Aza-Wittig Reaction of Sugar Isothiocyanates and Sugar Iminophosphoranes: An Easy Entry to Unsymmetrical Sugar Carbodiimides.;ChemInform;2010-08-03
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