196703-97-6

Upstream product

• 75-08-1 ethanethiol 
• 328047-23-0 ((1S,3R,4R,5S,6R)-4,5-Bis-benzyloxy-2,7-dioxa-bicyclo[4.1.0]hept-3-ylmethoxy)-triisopropyl-silane 
• 196703-95-4 1,5-anhydro-2-deoxy-3,4-di-O-benzyl-6-O-triisopropylsilyl-D-arabino-hex-1-enitol 

Downstream Products

• 196704-11-7 thioethyl 3,4-di-O-benzyl-2-O-pivaloyl-6-O-triisopropylsilyl-β-D-glucopyranoside 
• 196704-08-2 Benzoic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-ethylsulfanyl-6-triisopropylsilanyloxymethyl-tetrahydro-pyran-3-yl ester 
• 196704-14-0 4-Methoxy-benzoic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-2-ethylsulfanyl-6-triisopropylsilanyloxymethyl-tetrahydro-pyran-3-yl ester 
• 196704-01-5 thioethyl 3,4-di-O-benzyl-6-O-triisopropylsilyl-β-D-mannopyranoside 
• 196704-23-1 ethyl 3,4-di-O-benzyl-2-O-pivaloyl-1-thio-6-O-triisopropylsilyl-β-D-mannopyranoside 
• 226919-70-6 ethyl 3,4-di-O-benzyl-2-O-pivaloyl-1-thio-β-D-mannopyranoside 
• 226919-73-9 thioethyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-glucopyranoside-(1->6)-3,4-di-O-benzyl-2-O-pivaloyl-β-D-mannopyranoside 

Relevant academic research and scientific papers

Oligosaccharide synthesis with glycosyl phosphate and dithiophosphate triesters as glycosylating agents

Described is an efficient one-pot synthesis of α- and β-glycosyl phosphate and dithiophosphate triesters from glycals via 1,2-anhydrosugars. Glycosyl phosphates function as versatile glycosylating agents for the synthesis of β-glucosidic, β-galactosidic,

Coupling of glycal derived thioethyl glycosyl donors with glycal acceptors. An advance in the scope of the glycal assembly

Glycals were converted into thioethyl glycosyl donors through 1,2-anhydrosugar intermediates. Various participating groups in the C-2 position were examined for formation of β-glucosyl, β-galactosyl, and α-mannosyl linkages. A number of disaccharides was