7334-25-0

Upstream product

• 99679-76-2 Methyl-2-benzoylamino-3,4,6-tri-O-benzoyl-2-desoxy-β-D-glucopyranosid 
• 67-56-1 methanol 
• 98-88-4 benzoyl chloride 
• 32449-61-9 D-glucosamine 
• 1195233-55-6 methyl-(2-benzoylamino-2-deoxy-β-D-glucofuranoside) 

Downstream Products

• 99679-89-7 1,5-Anhydro-4,6-O-benzyliden-2-<(benzyloxycarbonyl)amino>-2-desoxy-D-erythro-hex-1-en-3-ulose 
• 99745-44-5 Methyl 2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 99745-45-6 Methyl 2-amino-4,6-O-benzylidene-2-N-benzyloxycarbonyl-2-deoxy-β-D-glucopyranoside 
• 99679-87-5 Methyl-4,6-O-benzyliden-2-<(benzyloxycarbonyl)amino>-2-desoxy-2-C-methyl-β-D-ribohexopyranosid-3-ulose 
• 99780-76-4 Methyl-4,6-O-benzyliden-2-<(benzyloxycarbonyl)amino>-2-desoxy-β-D-ribo-hexopyranosid-3-ulose 
• 99679-88-6 Methyl-4,6-O-benzyliden-2-<(benzyloxycarbonyl)amino>-2-desoxy-2-C,3-O-dimethyl-β-D-erythro-hex-3-enopyranosid 
• 99745-43-4 Methyl-2-benzoylamino-4,6-O-benzyliden-2-desoxy-β-D-glucopyranosid 

Relevant academic research and scientific papers

PALLADIUM(II) PROMOTED CARBOCYCLISATION OF AMINODEOXYHEX-5-ENOPYRANOSIDES

Under catalytic condicions, Pd(II) salts effect the clean conversion of aminodeoxyhex-5-enopyranosides 7 into the corresponding 3-hydroxy cyclohexanones 8.

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