795305-88-3

Upstream product

• 795305-86-1 phenyl 3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-1-thio-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 176798-33-7 2,2,3,3-tetramethoxybutane 
• 2936-70-1 (2R,3S,4S,5R,6S)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 

Downstream Products

• 864966-93-8 phenyl 2,6-di-O-benzyl-1-thio-β-D-glucopyranoside 
• 518332-41-7 2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-1-phenylsulfinyl-β-D-glucopyranoside 
• 943230-21-5 phenyl 2,6-O-benzyl-3,4,O-(butane-2,3-diyl)-1-thio-β-D-glucopyranoside 
• 518332-46-2 5-deoxy-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-5-phenyl-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose 
• 518332-60-0 3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-α-D-glucopyranosyl]-1,2-O-isopropylidene-5-phenyl-α-D-ribofuranose 

Relevant academic research and scientific papers

Design and synthesis of 5′-deoxy-5′-phenyladenophostin A, a highly potent IP3 receptor ligand

5′-Deoxy-5′-phenyladenophostin A (5), designed as a useful IP3 receptor ligand based on the previous structure-activity relationship studies, was successfully synthesized via two key stereoselective glycosidation steps. This compound proved to

Stereocontrolled formation of β-glucosides and related linkages in the absence of neighboring group participation: Influence of a trans-fused 2,3-O-carbonate group

Phenyl 4,6-di-O-benzyl-2,3-O-carbonyl-β-D-glucothiopyranoside and the regiosiomeric phenyl 2,6-di-O-benzyl-3,4-O-carbonyl-β-D-glucothiopyranoside were prepared and studied as glucosyl donors at -60 °C in dichloromethane with preactivation by 1-benzenesulf