107909-03-5

Upstream product

• 82305-37-1 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranosyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 64-19-7 acetic acid 

Downstream Products

• 136090-79-4 O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1-> 4')-(6'-O-acetyl-2',3'-di-O-benzyl-α-D-glucopyranosyl) 2,3,6-tri-O-benzyl-α-D-glucopyranose 
• 136090-78-3 O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1-> 4')-2',3',6'-tri-O-benzyl-α-D-glucopyranosyl) 6-O-acetyl-2,3-di-O-benzyl-α-D-glucopyranoside 
• 136090-74-9 6'-O-acetyl-2',3'-di-O-benzyl-α-D-glucopyranosyl 2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 136090-72-7 2,3,6-Tri-O-benzyl-α-D-glucopyranosyl 2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 136090-75-0 6'-O-acetyl-2',3'-di-O-benzyl-α-D-glucopyranosyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 

Relevant academic research and scientific papers

α-D-Glycosyl-Substituted α,α-D-Trehaloses with (1 -> 4)-Linkage: Syntheses and NMR Investigations

Two symmetrical trehalose glycosyl 'acceptors' 4 and 6 were prepared and three of the unsymmetrical type, 8, 10, and 11.Glucosylation of symmetrical 'acceptor'4 gave a higher yield of trisaccharide (44percent) than protective-group manipulation, namely vi