94898-44-9

Upstream product

• 43179-48-2 L-arabinose di(ethylthio)acetal 
• 76-83-5 trityl chloride 
• 532-20-7 L-arabinose 
• 38029-69-5 α-L-arabinofuranoside 

Downstream Products

• 94898-36-9 (2R,3S,4S,5S)-dimethyl 2-acetoxy-3,4,5-tribenzyloxy-1,1-cyclohexane dicarboxylate 
• 94898-35-8 (2R,3S,4S,5S)-2methyl-3,4,5-tribenzyloxytetrahydropyran 
• 94898-39-2 (1S,2S,3S,4S,5S)-4-acetoxy-5-acetoxymethyl-1,2,3-tribenzyloxycyclohexane 
• 94898-39-2 (1S,2S,3S,4R,5R)-4-acetoxy-5-acetoxymethyl-1,2,3-tribenzyloxycyclohexane 
• 94921-22-9 (3S,4S,5S)-3,4,5-Tris-benzyloxy-2-hydroxy-cyclohexane-1,1-dicarboxylic acid dimethyl ester 
• 94898-37-0 (3S,4S,5S)-3,4,5-Tris-benzyloxy-cyclohex-1-enecarboxylic acid methyl ester 
• 94943-07-4 (1S,2S,3S,4S,5S)-5-(acetoxymethyl)cyclohexane-1,2,3,4-tetrayl tetraacetate 
• 94898-38-1 (3S,4S,5S)-3,4,5-tribenzyloxy-1-hydroxymethyl-1-cyclohexene 
• 81307-66-6 (1S,2S,3S,4S,5S)-pseudo-β-L-altrose 
• 81307-66-6 (1S,2S,3S,4R,5R)-pseudo-α-D-glucose 
• 94898-47-2 Toluene-4-sulfonic acid (2S,3S,4R)-2,3,4-tris-benzyloxy-5,5-bis-ethylsulfanyl-pentyl ester 
• 94898-48-3 Toluene-4-sulfonic acid (2S,3S,4R)-2,3,4-tris-benzyloxy-5-oxo-pentyl ester 
• 94898-49-4 2,3,4-tri-O-benzyl-5-deoxy-5-iodo-L-arabinose 
• 94943-06-3 (1S,2S,3S,4R,5R)-1,2,3,4-tetraacetoxy-5-acetoxymethylcyclohexane 

Relevant academic research and scientific papers

Synthesis of substituted imidazolo[1,2-α]piperidinoses and their evaluation as glycosidase inhibitors

The synthesis of substituted imidazolo[1,2-α]-L-arabino-piperidinoses is reported. The substituents are methyl, phenylmethyl, phenylethyl, cyclohexylethyl, pyridinylethyl, piperidinylethyl, phenylpropyl and hydroxymethyl. All substituents are connected to

Increasing the inhibitory potency of L-arabino-imidazolo-[1,2]-piperidinose towards β-D-glucosidase and β-D-galactosidase

The synthesis of some potent inhibitors of two retaining β-glycosidases was achieved by introducing aglycon-mimics into the imidazole moiety of L-arabino azasugar 1. The strongest inhibition was observed with the phenyl-ethyl substituent at C(2) of 1 agai

SYNTHESIS OF OPTICALLY ACTIVE PSEUDO-α-D-GLUCOSE AND PSEUDO-β-L-ALTROSE

Optically active two pseudo-sugars, pseudo-α-D-glucose and pseudo-β-L-altrose have been synthesized by cyclization of 2,3,4-tri-O-benzyl-5-deoxy-5-iodo-L-arabinose with dimethyl malonate in the presence of sodium hydride as a key reaction.