219313-12-9

Upstream product

• 219313-07-2 Methyl 2-O-allyl-4,6-di-O-benzyl-α-[*]-mannopyranoside 
• 195875-35-5 methyl 3-O-benzoyl-4,6-di-O-benzyl-α-D-glucopyranoside 
• 219313-10-7 Benzoic acid (2R,3R,4S,5R,6S)-3-benzyloxy-2-benzyloxymethyl-6-methoxy-5-trifluoromethanesulfonyloxy-tetrahydro-pyran-4-yl ester 
• 219313-09-4 methyl 2-O-allyl-3-O-benzoyl-4,6-di-O-benzyl-α-D-glucopyranoside 
• 219313-16-3 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranosyl chloride 
• 58341-71-2 Methyl 4,6-di-O-benzyl-α-D-glucopyranoside 
• 219313-11-8 methyl 2-azido-3-O-benzoyl-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranoside 
• 67-56-1 methanol 
• 219313-17-4 1,3-anhydro-2-azido-4,6-di-O-benzyl-2-deoxy-β-D-mannopyranose 

Downstream Products

• 219313-13-0 methyl 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranoside 

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.