Compounds > 1-6-anhydro-beta-glucopyranose

1-6-anhydro-beta-glucopyranose and thiophenol

1-6-anhydro-beta-glucopyranose has been researched along with thiophenol* in 1 studies

Other Studies

1 other study(ies) available for 1-6-anhydro-beta-glucopyranose and thiophenol

Article	Year
Utilization of nosylepimines of 1,6-anhydro-beta-D-hexopyranoses for the preparation of halogenated aminosaccharides. Carbohydrate research, 2003, Nov-21, Volume: 338, Issue:24 The aziridine ring cleavage of N-nosylepimines 3 and 7 having D-allo and D-manno configurations with halides led regioselectively to N-o-nitrobenzenesulfonylated 2-halo-3-amino- and 3-halo-2-amino-2,3-dideoxy derivatives of 1,6-anhydro-beta-D-glucopyranose 8-14 in 59-81% yields. Removal of o-nitrobenzenesulfonyl protecting group with benzenethiol afforded aminosaccharides, which were converted into more stable hydrochlorides 15-18. Topics: Amino Sugars; Aziridines; Benzenesulfonates; Chromatography, Thin Layer; Cyclization; Glucose; Halogens; Magnetic Resonance Spectroscopy; Molecular Structure; Nitrobenzenes; Phenols; Stereoisomerism; Sulfhydryl Compounds	2003

Article

Year

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

Carbohydrate research, 2003, Nov-21, Volume: 338, Issue:24

The aziridine ring cleavage of N-nosylepimines 3 and 7 having D-allo and D-manno configurations with halides led regioselectively to N-o-nitrobenzenesulfonylated 2-halo-3-amino- and 3-halo-2-amino-2,3-dideoxy derivatives of 1,6-anhydro-beta-D-glucopyranose 8-14 in 59-81% yields. Removal of o-nitrobenzenesulfonyl protecting group with benzenethiol afforded aminosaccharides, which were converted into more stable hydrochlorides 15-18.

Topics: Amino Sugars; Aziridines; Benzenesulfonates; Chromatography, Thin Layer; Cyclization; Glucose; Halogens; Magnetic Resonance Spectroscopy; Molecular Structure; Nitrobenzenes; Phenols; Stereoisomerism; Sulfhydryl Compounds

2003