4097-98-7

Upstream product

• 29600-81-5 methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-galactopyranoside 
• 112260-57-8 methyl 2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 19488-48-3 methyl 2,3,6-tri-O-benzyl-α-D-galactopyranoside 
• 68622-25-3 Methyl 4-azido-2,3,6-tri-O-benzyl-4-deoxy-α-D-glucopyranoside 

Downstream Products

• 152581-83-4 [1-Benzyl-piperidin-(2E)-ylidene]-((2S,3R,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl)-amine 
• 182550-36-3 [(2R,3R,4S)-2,3,4-Tris-benzyloxy-4-((2S,3R,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-ylcarbamoyl)-butyl]-carbamic acid tert-butyl ester 
• 556062-89-6 methyl 2,3,6-tri-O-benzyl-4-amino-4-deoxy-4-N-(5'-benzyloxy-6'-benzyloxymethyl-2'-pyridyl)-α-D-glucopyranoside 

Relevant academic research and scientific papers

Syntheses of trehazolin derivatives and evaluation as glycosidase inhibitors

The trehazolin derivatives 9-12 were synthesized from the aminocyclitol (7), which is the degradation product of trehazolin (5). In particular, compounds 9-11 were pseudodisaccharides that underwent replacement of the corresponding nonreducing D-glucose m

Amidine pseudodisaccharides

The synthesis of several aminoglucopyranose-based amidine pseudodisaccharides is described. They may serve as glycosidase inhibitors by virtue of structural similarities to both the reducing and non-reducing pyranose units involved in glycolysis.