115886-91-4

Upstream product

• 100-39-0 benzyl bromide 
• 121843-59-2 methyl 2-acetamido-4-O-acetyl-3-O-<(R)-1'-benzylcarboxyethyl>-2-deoxy-6-O-tosyl-α,β-D-glucopyranoside 
• 121843-57-0 methyl 2-acetamido-4,6-O-benzylidene-3-O-<(R)-1'-benzylcarboxyethyl>-2-deoxy-α,β-D-glucopyranoside 
• 121843-56-9 methyl-4,6-O-benzylidene-muramic acid 
• 121843-58-1 methyl 2-acetamido-3-O-<(R)-1'-benzylcarboxyethyl>-2-deoxy-α,β-D-glucopyranoside 
• 121843-60-5 methyl 2-acetamido-4-O-acetyl-3-O-<(R)-1'-benzylcarboxyethyl>-2,6-dideoxy-6-iodo-α,β-D-glucopyranoside 
• 121843-61-6 methyl 2-acetamido-4-O-acetyl-3-O-<(R)-1'-benzylcarboxyethyl>-2-deoxy-α,β-D-xylo-hex-5-enopyranoside 

Downstream Products

• 115886-92-5 (R)-2-((1R,2R,3S,5S,6S)-2-Acetoxy-6-acetylamino-3,5-dihydroxy-cyclohexyloxy)-propionic acid benzyl ester 
• 121788-65-6 1D-(1,2,4/3,5)-2-acetamido-1,4,5-tri-O-acetyl-3-O-<(R)-1'-benzylcarboxyethyl>-1,3,4,5-cyclohexanetetrol 
• 115886-86-7 1D-(1,2,4/3,5)-2-acetamido-3-O-<(R)-2'-propanoyl-L-alanyl-D-isoglutamine>-1,3,4,5-cyclohexanetetrol 
• 115886-86-7 4-{(S)-2-[(R)-2-((1R,2S,3S,5S,6R)-2-Acetylamino-3,5,6-trihydroxy-cyclohexyloxy)-propionylamino]-propionylamino}-4-carbamoyl-butyric acid 
• 121788-67-8 1D-(1,2,4/3,5)-2-acetamido-1,4,5-tri-O-acetyl-3-O-<(R)-2'-propanoyl-L-alanyl-D-isoglutamine benzylester>-1,3,4,5-cyclohexanetetrol 
• 121788-66-7 1D-(1,2,4/3,5)-2-acetamido-1,4,5-tri-O-acetyl-3-O-<(R)-1'-carboxyethyl>-1,3,4,5-cyclohexanetetrol 

Relevant academic research and scientific papers

SYNTHETIC METHODS FOR THE PREPARATION OF BASIC D- AND L-PSEUDO-SUGARS. SYNTHESIS OF CARBOCYCLIC ANALOGUES OF N-ACETYL-MURAMYL-L-ALANYL-D-ISOGLUTAMINE (MDP)

Two exocyclic olefins 10 and 22, readily elaborated from D-glucosamine, have been transformed by Ferrier rearrangement reaction into aminocyclohexanones 11, 12 and 23, 24.Reduction of ketone 11 with tri-t-butoxy-aluminium hydride followed by sequential ac

Synthesis of Biologically Active Carbocyclic Analogues of N-Acetylmuramyl-L-alanyl-D-isoglutamine (MDP)

Two biologically active analogues of MDP containing pseudo-D-glucosamine have been synthesised using as key step the Ferrier rearrangement (carbohydrate inosose).Several different procedures for carrying out this reaction have been compared.