58341-56-3

Upstream product

• 15038-71-8 methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 106-95-6 allyl bromide 
• 100-39-0 benzyl bromide 
• 82228-10-2 methyl 3-O-allyl-4,6-O-benzylidene-α-D-mannopyranoside 

Downstream Products

• 20770-87-0 methyl 3-O-allyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 106444-77-3 8-methoxycarbonyloctyl-6-O-acetyl-3-O-allyl-2,4-di-O-benzyl-α-D-mannopyranosyl bromide 
• 106444-76-2 8-methoxycarbonyloctyl-6-O-acetyl-3-O-allyl-2,4-di-O-benzyl-β-D-mannopyranosyl bromide 
• 106444-75-1 methyl 6-O-acetyl-3-O-allyl-2,4-di-O-benzyl-α-D-mannopyranoside 
• 86861-45-2 1,6-Di-O-acetyl-3-O-allyl-2,4-di-O-benzyl-α-D-mannopyranose 
• 83259-13-6 6-O-acetyl-3-O-allyl-2,4-di-O-benzyl-α-D-mannopyranosyl bromide 
• 58341-60-9 Methyl 3-O-allyl-2,4-di-O-benzyl-α-D-glucopyranoside 
• 134311-55-0 Methyl 3-O-allyl-2,4-di-O-benzyl-6-deoxy-α-D-glucopyranoside 
• 142967-66-6 Methyl 3-O-allyl-2,4-di-O-benzyl-6-O-p-tolylsulfonyl-α-D-glucopyranoside 
• 142967-65-5 Methyl 3-O-allyl-2-O-benzyl-6-O-p-tolylsulfonyl-α-D-glucopyranoside 
• 114283-90-8 1,3-Di-O-acetyl-2,4-di-O-benzyl-6-deoxy-α,β-D-glucopyranose 
• 142967-67-7 Methyl 3-O-allyl-2,4-di-O-benzyl-6-deoxy-6-iodo-α-D-glucopyranoside 
• 127874-91-3 3-O-allyl-2,4-di-O-benzyl-6-deoxy-α/β-D-glucopyranose 
• 42822-31-1 2,4-Di-O-benzyl-6-deoxy-α,β-D-glucopyranose 

Relevant academic research and scientific papers

Synthesis and conformational analysis of substituted 2,6-dioxabicycloheptanes: 1,3-anhydro-2,4-di-O-benzyl-6-deoxy-β-D-glucopyranose by 1H-NMR spectroscopy and molecular mechanics calculation

A highly selective ring opening reduction of methyl 3-O-allyl-2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside provided the 2,4-di-O-benzyl derivative.This was toluenesulfonylated or iodinated and subsequently reduced to give crystalline methyl 3-O-allyl-

Design and synthesis of a trisubstrate analogue for α(1 →3)fucosyltransferase: A potential inhibitor

Phenyl 1-azido-3,4,5-tri-O-benzyl-I-deoxy-2-seleno-α-1-fuco-heptulopyranoside (5), readily accessible from perbenzylated 1-fucono-1,5-lactone, is a key intermediate in the preparation of trisubstrate analogue 2. NIS mediated condensation of fucosyl donor 5 with methyl 2,4,6-tri-O-benzyl-α-d-glucopyranoside (7) and ensuing reduction of the azido function furnished ketodisaccharide 10b, which was elongated at the 1-amino group of the fucose residue with a malonic acid spacer. The thus obtained compound was deprotected and subsequently coupled with 5′-amino-5′-deoxy-guanosine to afford the target compound 2.

Substrates for the differentiation of the N-acetylglucosaminyltransferases. Synthesis of βDGlcNAc(->2)αDMan(1->6)βDMan and βDGlcNAc(1->2)αDMan(1->6)3)βDMan glycosides

The trisaccharide βDGlcNAc(1->2)αDMan(1->6)βDMan (2) and the tetrasaccharide βDGlcNAc(1->2)αDMan(1->6)αDMan(1->3)>βDMan (3) have been chemically synthesized as their 8-methoxycarbonyloctyl glycosides.Compounds 2 and 3, both partial structures of naturally