67337-01-3

Usage

General Description

1,6-Anhydro-2-O-benzoyl-beta-D-galactopyranose is a chemical compound that belongs to the family of carbohydrates. It is a derivative of galactose and is commonly used in organic synthesis and as a starting material for the preparation of various glycosides and glycosylamines. 1,6-ANHYDRO-2-O-BENZOYL-BETA-D-GALACTOPYRANOSE is often utilized in the study of carbohydrate chemistry and plays a key role in the development of new drugs and pharmaceuticals. Additionally, 1,6-Anhydro-2-O-benzoyl-beta-D-galactopyranose has potential applications in the food industry, specifically in the production of novel sweeteners and flavor enhancers. Its unique structure and properties make it a valuable component in the field of organic and medicinal chemistry.

Upstream product

• 67307-84-0 1,6-Anhydro-2-O-benzoyl-3,4-O-isopropyliden-β-D-galactopyranose 
• 98-88-4 benzoyl chloride 
• 52579-97-2 1,6-anhydro-3,4-O-isopropylidene-β-D-galactopyranose 

Downstream Products

• 76909-70-1 3,4-Di-O-acetyl-1,6-anhydro-2-O-benzoyl-β-D-galactopyranose 
• 76909-69-8 1,6-Anhydro-2-O-benzoyl-3,4-O-(1-methoxyethyliden)-β-D-galactopyranose 
• 144542-85-8 Benzoic acid (1R,2R,3R,4R,5R)-3-hydroxy-2-trifluoromethanesulfonyloxy-6,8-dioxa-bicyclo[3.2.1]oct-4-yl ester 
• 161469-30-3 (1'R,2R,4S)-2-(2-O-Benzoyl-1-hydroxyethyl)-4-(hydroxymethyl)-1,3-dioxolane 
• 161469-31-4 (1'R,2R,4R)-4-<<(tert-Butyldiphenylsilyl)oxy>methyl>-2-(2-O-benzoyl-1-hydroxyethyl)-1,3-dioxolane 
• 144542-87-0 1,6-Anhydro-2-O-benzoyl-4-deoxy-4-β-D-glucopyranose 
• 144542-86-9 1,6-Anhydro-2-O-benzoyl-4-deoxy-4-iodo-β-D-glucopyranose 
• 76909-71-2 3-O-Acetyl-1,6-anhydro-2-O-benzoyl-β-D-galactopyranose 

Relevant academic research and scientific papers

Synthesis of L-dioxolane nucleosides and related chemistry

(+)-L- or (+)-(2R,4S)-1-[4-(hydroxymethyl)-1,3-dioxolan-2-yl]-5-fluorouracil (25) and other novel classes of 1,3-dioxolane nucleosides have been synthesized. Coupling of 2-methoxy-4-[[(tert-butyldiphenylsilyl)oxy]methyl]-1,3-dioxolane (23) or 2-methyl-1,3

Reactions of Some Pyranoside Diol Monotriflates with Nucleophiles and Bases

Reaction of pyranoside diol (equatorial) monotriflates with soft, nonbasic nucleophiles is a useful way to make axial heteroatom-substituted and "epimerized" pyranosides, particularly where a fused acetal ring inhibits ring contraction.Among the substrates examined (1,2,3,4,35), only 4 shows a strong tendency to give ring-contracted products.The reaction of 1-3 with more basic nucleophiles (F(1-), t-BuO(1-)) leads to the anhydrosugars 8, 25, and 26, respectively.The SN2 reaction of 35 with tetra n-butylammonium iodide forms the basis for a new synthesis of the Cerny epoxide 32.

Bausteine von Oligosacchariden, XXII. Synthese der Trisaccharid-Sequenz α-D-GlcNAc-(1-4)-β-D-Gal-(1-4)-D-GlcNAc aus blutgruppenaktiven Substanzen

A directly stereoselective α-glycoside synthesis to oligosaccharides succeeds in the presence of AgClO4/Ag2CO3 in methylene chloride with the α-bromide 1 of 2-azido-2-desoxy-D-glucose.By reaction with 1 the disaccharides 3, 7a, 7b, 18 and the trisaccharid