35905-39-6

Upstream product

• 72869-07-9 Benzyl 4,6-O-benzylidene-2,3-bis(O-methanesulfonyl)-α-D-glucopyranoside 
• 72869-08-0 benzyl 3-amino-4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside 
• 72869-09-1 benzyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-altropyranoside 
• 35905-30-7 Benzyl-4,6-O-benzyliden-2-O-p-tosyl-α-D-glucopyranosid 
• 79549-73-8 benzyl 4,6-O-(phenylmethylene)-α-D-glucopyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 34246-23-6 benzyl D-glucopyranoside 
• 100-52-7 benzaldehyde 
• 186697-04-1 benzyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 35905-38-5 Benzyl-4,6-O-benzyliden-2,3-bis-O-p-tosyl-α-D-glucopyranosid 

Downstream Products

• 81625-97-0 benzyl 2-azido-4,6-O-benzylidene-2-deoxy-α-D-altropyranoside 
• 81625-96-9 benzyl 3-azido-4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside 
• 81626-01-9 benzyl 2-azido-4,6-O-benzylidene-2-deoxy-α-D-threo-3-hexenopyranoside 
• 81626-00-8 benzyl 2,3-diazido-4,6-O-benzylidene-2,3-dideoxy-α-D-mannopyranoside 
• 72869-08-0 benzyl 3-amino-4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside 
• 72869-09-1 benzyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-altropyranoside 
• 61134-18-7 Benzyl-2,3-anhydro-α-D-allopyranosid 
• 104875-59-4 benzyl 2-azido-4,6-O-benzylidene-2,3-dideoxy-3-fluoro-α-D-altropyranoside 
• 127542-63-6 benzyl 4,6-O-benzylidene-3-deoxy-3-C-methyl-α-D-ribo-hexapyranoside-2-ulose 
• 127542-63-6 benzyl 4,6-O-benzylidene-3-deoxy-3-C-methyl-α-D-arabino-hexapyranoside-2-ulose 
• 127542-62-5 benzyl 4,6-O-benzylidene-3-deoxy-3-C-methyl-α-D-altropyranoside 
• 127542-62-5 benzyl 4,6-O-benzylidene-3-deoxy-3-C-methyl-α-D-glucopyranoside 
• 127542-75-0 benzyl 2-acetamido-6-O-benzyl-2,3-dideoxy-3-C-methyl-4-O-(2,3,4,6-tetra-O-acetyl-α/β-D-galactopyranosyl)-α-D-glucopyranoside 
• 127542-74-9 1,6-di-O-acetyl-2-O-benzoyl-3-deoxy-3-C-methyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-D-glucopyranose 

Relevant academic research and scientific papers

Regio- and Stereoselective Ring Opening of Epoxy Pyranosides with Titanium Isopropoxide Reagents and SmI2: A Straightforward Access to Iododeoxy Sugars

A regioselective synthesis of 3-iodo-3-deoxy sugars is described by trans-diaxial cleavage of the oxirane ring of 2,3-anhydropyranosides with halogenated titanium isopropoxide reagents and samarium iodide.

Prespacer Glycosides in Glycoconjugate Chemistry. Dibromoisobutyl Glycosides for the Synthesis of Neoglycolipids, Neoglycoproteins, Neoglycparticles, and Soluble Glycosides

3-Bromo-2-(bromomethyl)propyl (dibromoisobutyl or DIB) mono- to tetrasaccharide glycosides were prepared in moderate to high yields by treatment of the corresponding 1-O-acetyl saccharides with 3-bromo-2-(bromomethyl)propanol (DIBOL) and boron trifluoride

Evidence for Bicyclic Oxonium Ions in the Nitrous Acid Deamination of Benzyl 2-Amino-4,6-O-benzylidene-2-deoxy-D-glucopyranosides

The nitrous acid deamination of conformationally rigid benzyl amino-4,6-O-benzylidenedeoxy-D-hexopyranosides was studied: benzyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-altropyranoside (5) and benzyl 3-amino-4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside (4) in aqueous dioxane both gave some benzyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside (2).Thus, a trans-diaxial arrangement of hydroxyl and amino groups in the ground state does not appear to be an absolute requirement for epoxide formation, although such an arrangement clearly is most conducive to this reaction, as a comparision of yields showed.Benzyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-mannopyranoside (7) under similar conditions gave, by elimination, benzyl 4,6-O-benzylidene-α-D-erythro-hexopyrano-3-uloside (8) and, by benzyloxy migration, 2-O-benzyl-4,6-O-benzylidene-D-glucopyranose (11).Contrary to expectation, the same products, 8 and 11, were isolated from the deamination of benzyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside (10) and its α-D-mannopyranoside analogue (7).A bicyclic oxonium ion is postulated as an intermediate for the deamination of the α-D-gluco isomer.Benzyl 2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside (13), with nitrous acid, gave benzyl 4,6-O-benzylidene-2-deoxy-β-D-erythro-hexopyrano-3-uloside (14).Here also, a bicyclic oxonium ion appears to be involved.All products isolated in this or earlier work from the deamination of 2-amino-4,6-O-benzylidene-D-glucopyranosides can be explained by mechanisms involving bicyclic oxonium ion intermediates.Such intermediates are apparently not involved in the deamination of the manno or altro analogues.