Transformation of d-allose and l-gulose with potassium cyanate into cyclic carbamates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference24 articles.
1. Transformation of aldoses into glycosylamine 1,2-(cyclic carbamates) (glyco-oxazolidin-2-ones) by reaction with potassium cyanate
2. The crystal and molecular structure of α-D-ribofuro[l',2':4,5]-2-oxazolidone, a decomposition product of 5-azacytidine
3. Preparation of New Glycoheptofurano[2,1-d]Imidazolidine-2-Thiones., Isomerizations to Acyclic-SugarC-Nucleoside Analogues of Imidazole
4. Studies of the synthesis of 1,2-cis-(cyclic carbamates) of α-d-aldopyranosylamines
5. Carbon-13 Nuclear Magnetic Resonance Spectroscopy of Monosaccharides
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1. Direct formation and isolation of unprotected α-and β-d-ribopyranosyl urea, α-and β-d-ribofuranosyl urea, and a ribosyl-1,2-cyclic carbamate in carbohydrate melts;Carbohydrate Research;2020-06
2. ChemInform Abstract: Transformation of D-Allose and L-Gulose with Potassium Cyanate into Cyclic Carbamates.;ChemInform;2010-08-19
3. Short and General Procedure for Synthesizing Cis-1,2-Fused 1,3-Oxathiolan-, 1,3-Oxaselenolan-, and 1,3-Oxazolidin-2-imine Carbohydrate Derivatives;The Journal of Organic Chemistry;2009-12-15
4. Degradation and Rearrangement Reactions;Glycoscience: Chemistry and Chemical Biology I–III;2001
5. Synthesis of a new chiral oxazolidinone auxiliary based on d-xylose and its application to the Staudinger reaction;Tetrahedron: Asymmetry;2000-02
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