99679-75-1

Upstream product

• 99679-74-0 Methyl-4,6-O-benzyliden-2-desoxy-2-<(methoxycarbonyl)amino>-α-D-glucopyranosid 

Downstream Products

• 99679-74-0 Methyl-4,6-O-benzyliden-2-desoxy-2-<(methoxycarbonyl)amino>-α-D-glucopyranosid 
• 174582-79-7 methyl 4,6-O-benzylidene-2-deoxy-2-(methoxycarbonylamino)-α-D-allopyranoside 
• 651736-01-5 methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside 
• 1291090-68-0 methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->3)-2-deoxy-2-dimethylmaleimido-4,6-O-benzylidene-α-D-allopyranoside 
• 1291090-59-9 methyl 4,6-O-benzylidene-2-deoxy-2-dimethylmaleimido-α-D-allopyranoside 
• 174582-84-4 (4S,5S)-5-<(1R)-1-benzoyloxy-2-propen-1-yl>-4-cyanomethyl-2-oxazolidinone 
• 178738-22-2 (3aR,4S,5aR,8R,9aS,9bS)-4-Methoxy-8-phenyl-hexahydro-1,5,7,9-tetraoxa-3-aza-cyclopenta[a]naphthalen-2-one 
• 178550-56-6 Benzoic acid (4S,5R)-5-((E)-3-chloro-propenyl)-3-formyl-2-oxo-oxazolidin-4-ylmethyl ester 
• 178550-55-5 Benzoic acid (4S,5R)-5-((E)-3-chloro-propenyl)-2-oxo-oxazolidin-4-ylmethyl ester 
• 174582-80-0 methyl 2-amino-4-O-benzoyl-6-bromo-2,3-N,O-carbonyl-2,6-dideoxy-α-D-allopyranoside 
• 174582-83-3 (4S,5S)-4-benzyloxymethyl-5-<(1R)-1-hydroxy-2-propen-1-yl>oxazolidin-2-one 
• 174582-82-2 (4S,5S)-5-<(1R)-1-benzoyloxy-2-propen-1-yl>-4-hydroxymethyloxazolidin-2-one 
• 174582-81-1 (4R,5S)-5-<(1R)-1-benzoyloxy-2-propen-1-yl>-2-oxooxazolidin-4-carboxaldehyde 
• 99685-90-2 Methyl-4,6-O-benzyliden-2-desoxy-2-C-methyl-2-<(methoxycarbonyl)amino>-α-D-ribo-hexopyranosid-3-ulose 

Relevant academic research and scientific papers

A comparative study of the O-3 reactivity of isomeric N-dimethylmaleoyl- protected d-glucosamine and d-allosamine acceptors

Four isomeric N-dimethylmaleoyl 4,6-O-benzylidene-protected d-hexosamine acceptors (2, 3, 4, and 5) with all possible configurations at C-1 and C-3 (e.g., derived from d-glucosamine and d-allosamine) were prepared, and the assessment of their O-3 relative

Enolates of Carbohydrates, 4. - Axial C-Alkylation in α-Position of α-Amino-α-deoxy-ketoses

Products of type 2a-c, 6, 10a, b, and 14a, b which are alkylated in α-position of the keto function are yielded by reaction of the α-amino-α-deoxy-uloses 1a-c, 5, 9a, and 13a, b with LDA, CH3I, HMPA in THF (method A) or KOtBu, CH3I in DMF (method B) in a