329038-46-2

Upstream product

• 54769-36-7 N-benzoyloxybenzotriazole 
• 1253948-04-7 2-azido-2-deoxy-1,3,4,6-tetra-O-trimethylsilyl-D-glucopyranose 
• 100-52-7 benzaldehyde 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 93-97-0 benzoic acid anhydride 

Downstream Products

• 471891-12-0 Benzoic acid (2R,4aR,6S,7R,8R,8aR)-7-azido-2-phenyl-8-trifluoromethanesulfonyloxy-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl ester 
• 334834-34-3 4-O-(2-azido-2-deoxy-3,4-di-O-benzyl-6-O-benzoyl-α-D-glucopyranosyl)-2-O-benzoyl-3-O-benzyl-1,6-anhydro-β-L-idopyranose 
• 496780-24-6 2-azido-6-O-benzoyl-3,4-di-O-benzyl-2-deoxy-α,β-D-glucopyranose trichloroacetimidate 
• 334834-39-8 C₃₄H₃₁N₃O₇ 
• 334834-32-1 2-azido-2-deoxy-3,4-di-O-benzyl-β-D-glucopyranosyl benzoate 
• 471891-15-3 2-azido-3,4-di-O-benzyl-2-deoxy-β-D-allopyranosyl benzoate 
• 471891-14-2 Benzoic acid (2R,4aR,6S,7R,8S,8aS)-7-azido-8-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl ester 
• 471891-13-1 2-azido-4,6-O-benzylidene-2-deoxy-β-D-allopyranosyl benzoate 
• 334834-38-7 Benzoic acid (2R,4aR,6S,7R,8R,8aS)-7-azido-8-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl ester 

Relevant academic research and scientific papers

Regioselective and stereoselective benzoylation of 2-N-protected 4,6-O-ketal derivatives of D-glucosamines with 1-(benzoyloxy)benzotriazole

A highly regioelective and stereoselective benzoylation of the 2-N-protected 4,6-O-ketal derivatives of D-glucosamines with 1-(benzoyloxy)benzotriazole that affords the corresponding β anomeric benzoates in excellent yields is described herein.

Regioselective one-pot protection of d-glucosamine

A highly regioselective one-pot transformation of 2-azido-2-deoxy-1,3,4,6- tetra-O-trimethylsilyl-d-glucopyranose via sequential additions of various reagents was systematically studied, yielding the fully protected derivatives and the 1-, 3-, 4-, as well

Regioselective esterification of various D-glucopyranosides: Synthesis of a fully protected disaccharide unit of hyaluronic acid

A highly regioselective esterification of various D-glucopyranosides with triethylamine and acid anhydrides in excellent yields is described here. Its application toward the synthesis of a fully protected disaccharide unit of hyaluronic acid is also highlighted.

Synthesis of D-ribo-C18-phytosphingosine from D-glucosamine via the D-allosamine derivatives as key intermediates

A straightforward synthesis of D-ribo-C18-phytosphingosine from D-glucosamine hydrochloride in ten steps in 18.4% overall yield via the D-allosamine derivatives as key intermediates is described here.