133191-79-4

Upstream product

• 13096-62-3 (3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-one 
• 67-56-1 methanol 
• 131603-38-8 (5R,6R,7S,8R)-6,7,8-Tris-benzyloxy-5-benzyloxymethyl-1,4-dioxa-spiro[2.5]octane 
• 133191-78-3 3,4,5,7-tetra-O-benzyl-1-O-(methoxymethyl)-α,β-D-gluco-2-heptulopyranose 
• 133697-34-4 2,6-anhydro-3,4,5,7-tetra-O-benzyl-1-deoxy-D-gluco-hept-1-enitol 

Downstream Products

• 133191-84-1 2,6-anhydro-3,4,5-tri-O-benzyl-1-O-(trimethylacetyl)-7-O-(triphenylmethyl)-D-glycero-D-gulo-heptitol 
• 133191-80-7 3,4,5,7-tetra-O-benzyl-1-O-(trimethylacetyl)-α-D-gluco-2-heptulopyranose 
• 133191-81-8 2,6-anhydro-3,4,5,7-tetra-O-benzyl-1-O-(trimethylacetyl)-D-glycero-D-gulo-heptitol 
• 133191-87-4 2,6-anhydro-3,4,5-tri-O-benzyl-7-O-(trimethylacetyl)-L-glycero-L-gulo-heptonic acid 
• 133191-85-2 2,6-anhydro-3,4,5-tri-O-benzyl-1-O-(trimethylacetyl)-D-glycero-D-gulo-heptitol 
• 133191-86-3 2,6-anhydro-3,4,5-tri-O-benzyl-7-O-(trimethylacetyl)-aldehydo-L-glycero-L-gulo-heptose 
• 133191-83-0 2,6-anhydro-1-O-(trimethylacetyl)-7-O-(triphenylmethyl)-D-glycero-D-gulo-heptitol 
• 85398-14-7 3,4,5,7-tetra-O-benzyl-α-D-glycero-D-xylo-hept-2-ulopyranose 

Relevant academic research and scientific papers

Conversion of D-Glucose to L-Glucose: Oxidative Decarboxylation of α-Oxy Carboxylic Acids via Their Diacyl Peroxides

D-Glucose was converted to an L-glucose derivative.The key step was the oxidative decarboxylation of carboxylic acid 12 via its diacyl peroxide derivative.This synthetic scheme proceeds through C-glycosidic compounds and is applicable to other sugar confi

EPOXIDATION OF EXOCYCLIC GLYCALS: A NEW ACCESS TO GLYCOSIDES OF KETOSUGARS.

A novel approach to the synthesis of glycosides and disaccharides of ketofuranoses and ketopyranoses by epoxidation of exocyclic glycals and reaction of the intermediate epoxides with different alcohols is described.