135197-83-0

Upstream product

• 128135-55-7 3,4-di-O-acetyl-1-O-tert-butyldimethylsilyl-2,6-dideoxy-β-L-lyxo-hexopyranose 
• 108-98-5 thiophenol 
• 4551-15-9 phenylthiotrimethylsilane 
• 33650-60-1 methyl 3,4-di-O-acetyl-2,6-dideoxy-α-D-ribo-hexopyranoside 
• 882-33-7 diphenyldisulfane 
• 45742-40-3 2,6-dideoxy-D-lyxo-hexopyranose 
• 108-24-7 acetic anhydride 
• 141805-54-1 (2R,3R,4R)-2-Methyl-6-phenylsulfanyl-tetrahydro-pyran-3,4-diol 
• 4092-45-9 methyl 2,6-dideoxy-α-D-ribo-hexopyranoside 
• 127112-84-9 3,4-Di-O-acetyl-2,6-dideoxy-L-lyxo-hexopyranose 

Downstream Products

• 141805-54-1 (2R,3S,4S)-2-Methyl-6-phenylsulfanyl-tetrahydro-pyran-3,4-diol 
• 4409-79-4 S-phenyl benzenethiosulfinate 
• 167012-93-3 phenyl 2-deoxy-1-thio-α-L-fucopyranoside 
• 470456-68-9 thiophenyl 3-O-acetyl-4-azido-2,4,6-trideoxy-α-L-glucopyranoside 
• 167012-06-8 phenyl 3-O-benzoyl-2-deoxy-1-thio-α-L-fucopyranoside 
• 78464-95-6 methyl 3,4-di-O-acetyl-2,6-dideoxy-α-L-lyxo-hexopyranoside 
• 139190-80-0 Acetic acid (2R,3S,4R,6R)-3-acetoxy-6-cyclohexylmethoxy-2-methyl-tetrahydro-pyran-4-yl ester 
• 139190-79-7 Acetic acid (2R,3S,4R,6S)-3-acetoxy-6-cyclohexylmethoxy-2-methyl-tetrahydro-pyran-4-yl ester 
• 139190-72-0 (3aR,4R,7aS)-2,2,4-Trimethyl-6-phenylsulfanyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran 
• 139190-81-1 (3aR,4R,6S,7aS)-6-Cyclohexylmethoxy-2,2,4-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran 
• 139190-82-2 (3aR,4R,6R,7aS)-6-Cyclohexylmethoxy-2,2,4-trimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran 
• 161079-41-0 (2R,3S,4S,6R)-6-Cyclohexylmethoxy-2-methyl-tetrahydro-pyran-3,4-diol 
• 139190-84-4 Acetic acid (2R,3R,4S,6R)-3-acetoxy-6-cyclohexylmethoxy-2-methyl-tetrahydro-pyran-4-yl ester 
• 139190-83-3 Acetic acid (2R,3R,4S,6S)-3-acetoxy-6-cyclohexylmethoxy-2-methyl-tetrahydro-pyran-4-yl ester 

Relevant academic research and scientific papers

Method of forming multiple glycosidic linkages in a single step

The invention relates to methods that permit the rapid construction of oligosaccharides and other glycoconjugates. Methods for forming multiple glycosidic linkages in solution in a single step are disclosed. The invention takes advantage of the discovery

Solution and solid-phase formation of glycosidic linkages

The invention relates to methods that permit the rapid construction of oligosaccharides and other glycoconjugates. Methods for forming multiple glycosidic linkages in solution in a single step are disclosed. The invention takes advantage of the discovery

Highly stereoselective glycosylation by conformational assistance of glycosyl donor

Highly α-stereoselective glycosylation of 2-deoxy-D-fucose was achieved by use of the conformational assistance of the rigid glycosyl donor 2. The selectivity of the glycosylation of 2 was much higher than that of 3 which had a normal chair conformation.

2-Deoxy-1-O-silylated-β-hexopyranoses. Useful glycosyl donors and synthetic intermediates

Different 2-deoxy-1-O-silylated-β-hexopyranoses were synthesized with high degree of stereoselectivity and in high yield. Their application to direct synthesis of glycosides and glycosyl donors as well as other synthetically useful transformations at the