948036-07-5

Upstream product

• 948036-06-4 (2S,3S,4R,5R,6R)-2-allyloxy-3,5-bisbenzyloxy-6-[(tert-butyldimethylsilyl)oxy]methyl-tetrahydro-4H-pyran-4-yl acetate 
• 97576-59-5 allyl 2,4-di-O-benzyl-α-D-mannopyranoside 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 948036-05-3 (2S,3S,4S,5R,6R)-2-allyloxy-3,5-bisbenzyloxy-6-[(tert-butyldimethylsilyl)oxy]methyl-4-trifluoromethanesulfonyloxy-tetrahydro-4H-pyran 
• 948036-04-2 (2S,3S,4S,5S,6R)-2-allyloxy-3,5-bisbenzyloxy-6-[(tert-butyldimethylsilyl)oxy]methyl-tetrahydro-4H-pyran-4-ol 

Downstream Products

• 948036-11-1 2,3,4-tri-O-benzyl-6-O-tert-butyldimethylsilyl-1-C-vinyl-D-altropyranose 
• 948036-12-2 (1R,2R,3R,4S,5R)-2,3,4-tris(benzyloxy)-5-vinyl-6,8-dioxabicyclo[3.2.1]octane 
• 948036-10-0 (3S,4R,5R,6R)-6-[(tert-butyldimethylsilyl)oxy]methyl-3,4,5-trisbenzyloxy-tetrahydropyran-2-one 

Relevant academic research and scientific papers

Syntheses of a partially benzylated derivative of the anhydro-d-altro-heptulose found in Coriaria japonica A and of its analogs

A partially benzylated derivative of anhydro-d-altro-heptulose found in Coriaria japonica A, which is a synthetically useful unit, was successfully synthesized from a d-mannose derivative by a novel synthetic approach involving the intramolecular O-ketopy

Synthesis of a partially benzylated derivative of the anhydro-d-altro-heptulose found in Coriaria japonica A

A partially benzylated derivative of the anhydro-d-altro-heptulose found in Coriaria japonica A, which is a synthetically useful unit, was successfully synthesized from a d-mannose derivative by a novel synthetic approach involving an intramolecular O-ket