1158796-37-2

Upstream product

• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 903906-55-8 p–tolyl 2,3-O-isopropylidene-1-thio-α-L-rhammopyranoside 
• 1159181-00-6 p-tolyl 2,3,4-tri-O-benzyl-7-O-methyl-6-deoxy-1-thio-β-D-galacto-hept-6-enopyranoside 
• 132201-75-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose trichloroacetimidate 
• 479252-05-6 ((2R,3R,4S,5R,6S)-3,4,5-Tris-benzyloxy-6-p-tolylsulfanyl-tetrahydro-pyran-2-yl)-methanol 
• 131531-76-5 p-methylphenyl 2,3,4,6-tetra-O-benzyl-thio-β-D-glucopyranoside 
• 30608-21-0 1-O-trimethylsilyl-2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside 
• 106-45-6 para-thiocresol 

Relevant academic research and scientific papers

Solvent participation in a one-pot glycosylation strategy (SPOG)

Solvent participation in a one-pot glycosylation strategy (SPOG) was developed on the basis of the low concentration β-selective glycosylation method. This strategy enables the production of a β-glycosidic bond in a one-pot oligosaccharide synthesis without or with minimal use of any C-2 participating function.

Studies on Glycosides VII. A Highly Stereoselective Synthesis of 1-Thioglycosides

A facile method for the synthesis of 1-thioglycosides using 1-α-O-trimethylsilyl-2,3,4,6,-tetra-O-benzyl-D-gluco- or manno-pyranoside by the promotion of BF3Et2O was reported.The reaction conditions were very mild, and 1-thioglycosides were obtained in hi