870192-91-9

Upstream product

• 870192-82-8 Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-[3-(tert-butyl-dimethyl-silanyloxy)-3-cyano-propylsulfanyl]-tetrahydro-pyran-4-yl ester 
• 572-10-1 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl chloride 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 
• 29868-42-6 methyl 2,3-di-O-acetyl-α-D-glucopyranoside 
• 302783-17-1 methyl 2,3-di-O-acetyl-4,6-O-p-methoxybenzylidene-α-D-glucopyranoside 
• 162680-20-8 methyl 4,6-O-[(R)-(4-methoxyphenyl)methylene]-α-D-glucopyranoside 
• 870192-84-0 (2R,3R,4R,5R,6S)-4,5-Diacetoxy-3-[(2S,4aR,6R,7R,8S,8aS)-7,8-diacetoxy-2-(4-methoxy-phenyl)-hexahydro-pyrano[3,2-d][1,3]dioxin-6-ylsulfanyl]-6-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 870192-85-1 (2R,3R,4R,5R,6S)-4,5-Diacetoxy-3-((2R,3R,4S,5S,6R)-3,4-diacetoxy-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-2-ylsulfanyl)-6-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 870192-86-2 C₂₃H₃₂O₁₆S 
• 870192-83-9 Acetic acid (2S,4aR,6R,7R,8S,8aS)-7-acetoxy-6-[3-(tert-butyl-dimethyl-silanyloxy)-3-cyano-propylsulfanyl]-2-(4-methoxy-phenyl)-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl ester 
• 874634-84-1 2-(tert-Butyl-dimethyl-silanyloxy)-4-[(2S,4aR,6R,7R,8R,8aR)-7,8-dihydroxy-2-(4-methoxy-phenyl)-hexahydro-pyrano[3,2-d][1,3]dioxin-6-ylsulfanyl]-butyronitrile 
• 870192-81-7 (2S,3S,4R,5R,6S)-4,5-Diacetoxy-6-methoxy-3-trifluoromethanesulfonyloxy-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 380224-05-5 2,3,4,6-tetra-O-acetyl-1-thio-D-galactopyranose 
• 870192-80-6 (2S,3S,4S,5R,6S)-4,5-Diacetoxy-3-hydroxy-6-methoxy-tetrahydro-pyran-2-carboxylic acid methyl ester 

Downstream Products

• 870192-89-5 C₅₄H₆₆O₂₅S 

Relevant academic research and scientific papers

Design, synthesis, and enzymatic property of a sulfur-substituted analogue of trigalacturonic acid

A sulfur-substituted analogue of trigalacturonic acid (3) was synthesized. The synthesis features the application of 3-cyano-3-(tert-butyldimethylsilyl) oxypropylthioether (CSP) as a novel protective group for thiols. This analogue was designed with the expectation that it would be a stable analogous substrate for endo-polygalacturonase isolated from Stereum purpureum based on computer modeling experiments. Surface plasmon resonance experiments revealed that 3 forms a stable complex with the target enzyme.