196397-58-7

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 261374-57-6 phenyl 1-thio-α-L-fucopyranoside 
• 75-77-4 chloro-trimethyl-silane 
• 16029-98-4 trimethylsilyl iodide 
• 73-34-7 6-deoxy-L-galactose 
• 108-98-5 thiophenol 
• 127061-11-4 phenyl 1-thio-α/β-L-fucopyranoside 
• 492440-44-5 1,2,3,4-tetrakis(oxy)tetrakis(trimethylsilane) L-Fucose 
• 127061-10-3 phenyl 2,3,4-tri-O-acetyl-1-thio-L-fucopyranoside 

Downstream Products

• 215364-17-3 phenyl 1-oxo-3,4-O-isopropylidene-1-thio-α-L-fucopyranoside 

Relevant academic research and scientific papers

Synthesis of fully protected α-l-fucopyranosyl-(1→2)-β-d- galactopyranosides with a single free hydroxy group at position 2′, 3′ or 4′ using O-(2-naphthyl)methyl (NAP) ether as a temporary protecting group

Perbenzylated methyl α-l-fucopyranosyl-(1→2)-β-d- galactopyranosides having a single free OH group at position C-2′, C-3′ or C-4′ have been synthesized. Methyl 3,4,6-tri-O-benzyl- β-d-galactopyranoside was glycosylated either with phenyl 3,4-di-O-benzyl-2

Stereoselective synthesis of carba- and C-glycosyl analogs of fucopyranosides

Fucopyranoside analogs with methylene groups instead of endo- or exo- anomeric oxygens, carba- and C-fucopyranosides, respectively, were synthesized. For the synthesis of 5a-carba-L-fucose (1) two approaches were studied, which shared a common cyclitol bu

Glycosyl phenyl sulfoxides as a source of glycosyl carbanions: Stereoselective synthesis of C-fucosides

Phenylsulfmyl-lithium exchange on glycosyl phenyl sulfoxides leads to configurationally stable anomeric carbanions which can react stereoselectively with electrophiles. Thus, the reaction of 3,4-O- isopropylidene-α-L-fucopyranosyl phenyl sulfoxide with tB