87591-34-2

Upstream product

• 4548-45-2 2-chloro-5-nitropyridine 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 55287-35-9 (2R,4aR,6R,7R,8R,8aS)-6-((2R,3S,4R,5R,6R)-4,5-Dihydroxy-2-hydroxymethyl-6-phenoxy-tetrahydro-pyran-3-yloxy)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 87591-17-1 Phenyl-O-(2,3-di-O-benzyl-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranosid 
• 87591-15-9 Phenyl-O-(2,3-di-O-benzyl-4,6-O-benzyliden-α-D-glucopyranosyl)-(1->4)-2,6-di-O-benzyl-α-D-glucopyranosid 
• 87591-14-8 Phenyl-O-(2,3-di-O-benzyl-4,6-O-benzyliden-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranosid 
• 87591-30-8 Phenyl-O-<2,3,6-tri-O-benzyl-4-O-(5-nitropyridin-2-yl)-α-D-glucopyranosyl>-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranosid 
• 87591-19-3 Phenyl-O-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranosid 

Relevant academic research and scientific papers

α-Glucosidases Inhibitors, 1. - Synthesis of Modified Maltoses

The easily available phenyl maltoside 1 was selectively transformed into the partially protected compounds 2, 5, and 7-9, respectively.From the 4',6'-unprotected maltose derivative 7 the 6'-deoxymaltoside 12 was obtained in three steps and in good yields.