135583-76-5

Upstream product

• 65827-55-6 1,2-di-O-acetyl-3,4,6-tri-O-benzyl-α-D-glucopyranoside 
• 645-96-5 Benzeneselenol 
• 89016-59-1 2-O-acetyl-3,4,6-tri-O-benzyl-D-glucopyranosyl chloride 
• 29073-91-4 (3aR,5R,6S,7S,7aR)-5-Hydroxymethyl-2-methoxy-2-methyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6,7-diol 
• 3254-16-8 3,4,6-tri-O-acetyl-[1,2-O-(1-methoxyethylidene)]-α-D-glucopyranose 
• 158852-31-4 3,4,6-tri-O-benzyl-1,2-O-(exo-ethoxyethylidene)-α-D-glucopyranose 
• 51532-75-3 3,4,6-tri-O-benzyl-1,2-O-(1-methoxyethylidene)-α-D-glucopyranose 

Downstream Products

• 128775-58-6 (2R,3R,4S,5R,6S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-5-(1-methoxy-allyloxy)-6-phenylselanyl-tetrahydro-pyran 
• 128775-57-5 ((2S,3R,4S,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenylselanyl-tetrahydro-pyran-3-yloxy)-methoxy-acetaldehyde 
• 128775-68-8 [(R)-2-((2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-methoxy-tetrahydro-pyran-2-yl)-propoxy]-tert-butyl-diphenyl-silane 
• 128775-67-7 (3S,3aR,5R,6R,7S,7aS)-6,7-Bis-benzyloxy-5-benzyloxymethyl-3-methyl-hexahydro-furo[3,2-b]pyran-2-one 
• 128775-66-6 (3R,3aR,5R,6R,7S,7aS)-6,7-Bis-benzyloxy-5-benzyloxymethyl-3-methyl-hexahydro-furo[3,2-b]pyran-2-one 
• 455929-00-7 phenyl 2-O-(prop-1-enyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside 
• 128775-69-9 phenyl 2-O-allyl-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside 
• 128775-56-4 phenyl 3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside 
• 135636-96-3 (3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenylselanyl-tetrahydro-pyran-3-ol 
• 135560-95-1 ((3R,4S,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-phenylselanyl-tetrahydro-pyran-3-yloxy)-dimethyl-phenylethynyl-silane 
• 135560-96-2 (2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((E)-styryl)-tetrahydro-pyran-3-ol 
• 135561-09-0 (2R,3S,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-hydroxymethyl-tetrahydro-pyran-3-ol 

Relevant academic research and scientific papers

Stereoselective 1,2-cis glycosylation of 2-O-Allyl protected thioglycosides

The technique of intramolecular aglycon delivery (IAD), whereby a glycosyl acceptor is temporarily appended to a hydroxyl group of a glycosyl donor is an attractive method that can allow the synthesis of 1,2-cis glycosides in an entirely stereoselective f

Synthesis of the C-glycosidic analogue of adenophostin A and its uracil congener as potential IP3 receptor ligands. Stereoselective construction of the C-glycosidic structure by a temporary silicon-tethered radical coupling reaction

Synthesis of the C-glycosidic analogue 9 of adenophostin A, a very potent IP3 receptor agonist, and its uracil congener 10 was achieved via a temporary silicon-tethered radical coupling reaction as the key step. Phenyl 3,4,6-tri-O-(p-methoxyben

STEREOSELECTIVE C-C BOND FORMATION IN CARBOHYDRATES BY RADICAL CYCLIZATION REACTIONS -- IV. APPLICATION FOR THE SYNTHESIS OF α-C(1)-GLUCOSIDES.

The synthesis of α-C(1)-glucosides is reported using our new strategy for the C-C bond formation at the anomeric center by radical cyclization reactions.