89016-60-4

Upstream product

• 2280-44-6 D-Glucose 
• 100-44-7 benzyl chloride 
• 107-18-6 allyl alcohol 

Downstream Products

• 88988-65-2 Chloro-acetic acid (2R,3R,4S,5R,6S)-6-((2R,3R,4S,5R,6R)-6-allyloxy-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethoxy)-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl ester 
• 88988-67-4 Chloro-acetic acid (2R,3R,4S,5R,6R)-6-((2R,3R,4S,5R,6R)-6-allyloxy-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethoxy)-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl ester 
• 88988-66-3 allyl O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-O-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 88988-63-0 Chloro-acetic acid (2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-hydroxy-tetrahydro-pyran-2-ylmethyl ester 
• 88988-64-1 Chloro-acetic acid (2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-chloro-tetrahydro-pyran-2-ylmethyl ester 
• 289898-48-2 Octadecanoic acid 2-((2R,3R,4S,5S,6S)-6-acetylsulfanylmethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-yloxy)-1-octadecanoyloxymethyl-ethyl ester 
• 760178-15-2 Octadecanoic acid 3-((2R,3R,4S,5S,6S)-6-acetylsulfanylmethyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-yloxy)-2-hydroxy-propyl ester 
• 289898-47-1 Thioacetic acid S-[(2S,3S,4S,5R,6R)-3,4,5-tris-benzyloxy-6-(2,3-dihydroxy-propoxy)-tetrahydro-pyran-2-ylmethyl] ester 
• 289898-46-0 Thioacetic acid S-((2S,3S,4S,5R,6R)-6-allyloxy-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl) ester 
• 267900-41-4 1-O-allyl-2,3,4-tri-O-benzyl-β-D-glucose 6-O-tosylate 
• 88988-62-9 Chloro-acetic acid (2R,3R,4S,5R,6R)-6-allyloxy-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-ylmethyl ester 
• 136310-59-3 allyl O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-β-D-glucopyranoside 
• 146773-72-0 allyl O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Structurally Simple Benzyl-Type Photolabile Protecting Groups for Direct Release of Alcohols and Carboxylic Acids

Structurally simple benzyl-type photolabile protecting groups (PPGs) have been developed to release alcohols and carboxylic acids. Release of two substrates from one PPG chromophore has also been accomplished. (Chemical Equation Presented).

DIOXA-BICYCLO[3.2.1]OCTANE-2,3,4-TRIOL DERIVATIVES

Compounds of Formula (A) and (B) are described herein and the uses thereof for the treatment of diseases, conditions and/or disorders mediated by sodium-glucose transporter inhibitors (in particular, SGLT2 inhibitors).