577995-63-2

Upstream product

• 577995-59-6 (2S,3R,4S)-2,3,4-tris(benzyloxy)-4-(1H-imidazol-2-yl)butan-1-ol 
• 577995-58-5 2-[(1S,2R,3S)-1,2,3-tris(benzyloxy)-4-(trityloxy)butyl]-1H-imidazole 

Downstream Products

• 577995-67-6 (6S,7S,8S)-6,7,8-tris(benzyloxy)-2-(phenylethynyl)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine 
• 577995-65-4 (6S,7S,8S)-6,7,8-tris(benzyloxy)-3-(phenylethynyl)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine 
• 577995-73-4 {(6S,7S,8S)-6,7,8-tris(benzyloxy)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridin-2-yl}methanol 
• 577995-70-1 {(6S,7S,8S)-6,7,8-tris(benzyloxy)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridin-3-yl}methanol 
• 577995-62-1 (6S,7S,8S)-6,7,8-tris(benzyloxy)-2-iodo-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine 
• 577995-72-3 (6S,7S,8S)-6,7,8-tris(benzyloxy)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine-2-carbaldehyde 
• 577995-69-8 (6S,7S,8S)-6,7,8-tris(benzyloxy)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine-3-carbaldehyde 
• 882692-62-8 (6S,7S,8S)-6,7,8-tris(benzyloxy)-2,3-bis(phenylethynyl)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine 
• 882692-58-2 (6S,7S,8S)-6,7,8-tris(benzyloxy)-3-(cyclohex-1-enylethynyl)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine 
• 882692-59-3 (6S,7S,8S)-6,7,8-tris(benzyloxy)-2-(cyclohex-1-enylethynyl)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine 
• 882692-63-9 {(6S,7S,8S)-6,7,8-tris(benzyloxy)-2-(phenylethynyl)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridin-3-yl}methanol 
• 882692-57-1 (6S,7S,8S)-6,7,8-tris(benzyloxy)-2-(3-phenylprop-1-ynyl)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine 
• 882692-61-7 (6S,7S,8S)-6,7,8-tris(benzyloxy)-2-(pyridin-2-ylethynyl)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine 
• 882692-60-6 (6S,7S,8S)-6,7,8-tris(benzyloxy)-3-(pyridin-2-ylethynyl)-5,6,7,8-tetrahydroimidazol[1,2-a]pyridine 

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