Utilization of nosylepimines of 1,6-anhydro-β-D-hexopyranoses for the preparation of halogenated aminosaccharides

Carbohydrate Research

Volumn 338, Issue 24, 2003, Pages 2825-2833

  Kroutil, Jiří ^a   Karban, Jindřich ^b   Buděšínský, Miloš ^c  

^a CHARLES UNIVERSITY   (Czech Republic)

^b INSTITUTE OF CHEMICAL PROCESS FUNDAMENTALS   (Czech Republic)

^c INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

Author keywords

Aziridines; Nitrobenzenesulfonamides; NMR data; Ring opening reactions; Stereospecific synthesis

Indexed keywords

DERIVATIVES; HYDROGEN INORGANIC COMPOUNDS;

HALIDES;

CARBOHYDRATES;

1,6 ANHYDRO 4 O BENZYL 2 BROMO 2,3 DIDEOXY 3 (N 2 NITROBENZENESULFONYLAMINO) BETA DEXTRO GLUCOPYRANOSE; 1,6 ANHYDRO 4 O BENZYL 2 CHLORO 2,3 DIDEOXY 3 (N 2 NITROBENZENESULFONYLAMINO) BETA DEXTRO GLUCOPYRANOSE; 1,6 ANHYDRO 4 O BENZYL 2,3 DIDEOXY 2 FLUORO 3 (N 2 NITROBENZENESULFONYLAMINO) BETA DEXTRO GLUCOPYRANOSE; 1,6 ANHYDRO 4 O BENZYL 2,3 DIDEOXY 2 IODO 3 (N 2 NITROBENZENESULFONYLAMINO) BETA DEXTRO GLUCOPYRANOSE; 1,6 ANHYDRO 4 O BENZYL 2,3 DIDEOXY 2,3 (N 2 NITROBENZENESULFONYLEPIMINO) BETA DEXTRO ALLOPYRANOSE; 1,6 ANHYDRO 4 O BENZYL 2,3 DIDEOXY 2,3 (N 2 NITROBENZENESULFONYLEPIMINO) BETA DEXTRO MANNOPYROSE; 1,6 ANHYDRO 4 O BENZYL 2,3 DIDEOXY 3 IODO 2 (N 2 NITROBENZENESULFONYLAMINO) BETA DEXTRO GLUCOPYRANOSE; 1,6 ANHYDRO 4 O BENZYL 3 BROMO 2,3 DIDEOXY 2 (N 2 NITROBENZENESULFONYLAMINO) BETA DEXTRO GLUCOPYRANOSE; 1,6 ANHYDRO 4 O BENZYL 3 CHLORO 2,3 DIDEOXY 2 (N 2 NITROBENZENESULFONYLAMINO) BETA DEXTRO GLUCOPYRANOSE; 3 AMINO 1,6 ANHYDRO 4 O BENZYL 2 BROMO 2,3 DIDEOXY BETA DEXTRO GLUCOPYRANOSE; 3 AMINO 1,6 ANHYDRO 4 O BENZYL 2 CHLORO 2,3 DIDEOXY BETA DEXTRO GLUCOPYRANOSE; 3 AMINO 1,6 ANHYDRO 4 O BENZYL 2,3 DIDEOXY 2 FLUORO BETA DEXTRO GLUCOPYRANOSE; 3 AMINO 1,6 ANHYDRO 4 O BENZYL 2,3 DIDEOXY 2 IODO BETA DEXTRO GLUCOPYRANOSE; AMINOSUGAR; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; HALOGENATION; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; RING OPENING; STEREOCHEMISTRY;

EID: 0345600070     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2003.07.003     Document Type: Article

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