219313-07-2

Upstream product

• 58341-71-2 Methyl 4,6-di-O-benzyl-α-D-glucopyranoside 
• 106-95-6 allyl bromide 

Downstream Products

• 125365-14-2 Methyl 2-O-allyl-4,6-di-O-benzyl-3-O-(2,3,4,6-tetra-O-benzyl-α-<*>-galactopyranosyl)-α-<*>-mannopyranoside 
• 125365-18-6 Methyl 2-O-allyl-4,6-di-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-<*>-galactopyranosyl)-α-<*>-mannopyranoside 
• 7115-19-7 Methyl 3-O-β-<*>-galactopyranosyl-α-<*>-mannopyranoside 
• 125365-16-4 Methyl 4,6-di-O-benzyl-2-O-(methyl 2,3,4-tri-O-acetyl-β-<*>-glucopyranosyluronate)-3-O-(2,3,4,6-tetra-O-benzyl-α-<*>-galactopyranosyl)-α-<*>-mannopyranoside 
• 125365-15-3 Methyl 4,6-di-O-benzyl-3-O-(2,3,4,6-tetra-O-benzyl-α-<*>-galactopyranosyl)-α-<*>-mannopyranoside 
• 125365-19-7 methyl 2-O-acetyl-4,6-di-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-<*>-galactopyranosyl)-α-<*>-mannopyranoside 
• 125365-17-5 Methyl 3-O-α-<*>-galactopyranosyl2-O-(β-<*>-glucopyranosyluronic acid)-α-<*>-mannopyranoside 
• 219313-10-7 Benzoic acid (2R,3R,4S,5R,6S)-3-benzyloxy-2-benzyloxymethyl-6-methoxy-5-trifluoromethanesulfonyloxy-tetrahydro-pyran-4-yl ester 
• 219313-11-8 methyl 2-azido-3-O-benzoyl-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranoside 
• 219313-13-0 methyl 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranoside 
• 219313-12-9 methyl 2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranoside 
• 195875-35-5 methyl 3-O-benzoyl-4,6-di-O-benzyl-α-D-glucopyranoside 
• 219313-09-4 methyl 2-O-allyl-3-O-benzoyl-4,6-di-O-benzyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis and glycosidic coupling reaction of substituted 2,6-dioxabicyco[3.1.1] heptanes: 1,3-anhydro-2-azido-4,6-di-O-benzyl-2-deoxy-β-D-mannopyranose

The title 1,3-anhydro sugar was synthesized from methyl α-D-glucopyranoside. The key intermediate for the synthesis was 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranosyl chloride (11) which was transformed into the target compound by ring closure with potassium tert-butoxide. Copyright (C) 1998 Elsevier Science Ltd.

SYNTHESIS OF A DI-AND A TRI-SACCHARIDE RELATED TO THE K-ANTIGEN OF Klebsiella TYPE 10 AND A STUDY OF THEIR INHIBITION IN THE PRECIPITIN REACTION

Synthesis of methyl 3-O-α--galactopyranosyl-α--mannopyranoside (10) and methyl 3-O-α--galactopyranosyl-2-O-(β--glucopyranosyluronic acid)-α--mannopyranoside (11) in good yield are described.Both 10 and 11 significantly inhibit antigen-antib