878800-58-9

Upstream product

• 792908-47-5 4-O-mesyl-6-O-benzyl-D-gulal 

Downstream Products

• 1408324-74-2 1,5-anhydro-3-azido-6-O-benzyl-2,3,4-trideoxy-4-(mesylamino)-D-xylo-hex-1-enitol 
• 878800-59-0 6-O-benzyl-3-deoxy-3-azido-D-glucal 
• 1408325-01-8 1,5-anhydro-6-O-benzyl-2,3,4-trideoxy-3-methyl-4-(mesylamino)-D-xylo-hex-1-enitol 
• 1404312-10-2 phenyl 6-O-benzyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 
• 1404312-16-8 cyclohexyl 6-O-benzyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 
• 1404312-11-3 benzyl 6-O-benzyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 
• 1404312-28-2 L-threonine N-[(1,1-dimethylethoxy)carbonyl]-O-(6-O-benzyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranosyl) methyl ester 
• 1404312-27-1 L-serine N-[(1,1-dimethylethoxy)carbonyl]-O-(6-O-benzyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranosyl) methyl ester 
• 1404312-24-8 L-tyrosine N-[(1,1-dimethylethoxy)carbonyl]-O-(6-O-benzyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranosyl) methyl ester 
• 1404312-32-8 methyl 4-O-(6'-O-benzyl-2',3'-dideoxy-α-D-erythro-hex-2'-enopyranosyl)-6-O-benzyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 
• 1404312-20-4 methyl 4-O-(6'-O-benzyl-2',3'-dideoxy-α-D-erythro-hex-2'-enopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 1404312-19-1 methyl 6-O-(6'-O-benzyl-2',3'-dideoxy-α-D-erythro-hex-2'-enopyranosyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 1404312-33-9 methyl 4-O-[4'-O-(6-O-benzyl-2,3-dideoxy-α-D-erythrohex-2-enopyranosyl)-6'-O-benzyl-2',3'-dideoxy-α-D-erythro-hex-2'-enopyranosyl]-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 

Relevant academic research and scientific papers

Palladium-catalyzed improved regio- and stereoselective O-glycosylation of D-glucal-derived β- And α-vinyl oxiranes

A Pd0-catalyzed glycosylation of D-glucal-derived vinyloxiranes as excellent glycosyl donors has been accomplished in a regio- and stereoselective manner. Various glycosyl acceptors upon reaction with vinyl oxiranes 1a and 1b produced the corre

Enantiopure cis- and trans-2,5-disubstituted-2,5-dihydrofurans from D-allal- and D-galactal-derived vinyl epoxides

Upon treatment with the metal enolates of methylene active compounds (dimethyl malonate and dibenzoylmethane) (C-nucleophiles) and benzyl carbamate (N-nucleophile), D-allal- and D-galactal-derived vinyl epoxides are stereoselectively transformed, in a sin

Stereoselective uncatalyzed synthesis of 2,3-unsaturated-4-N-substituted- β-O-glycosides by means of a new D-galactal-derived N-(mesyl)-aziridine

The reaction of the new D-galactal-derived allylic aziridine 1β with O-nucleophiles (alcohols and monosaccharides) affords, in a high to complete β-stereoselectivity, the corresponding 2,3-unsaturated-β-O-glycosides bearing a β-N-functionality at C(4).