32742-28-2

Upstream product

• 95-48-7 ortho-cresol 
• 604-69-3 β-D-glucose pentaacetate 
• 60523-66-2 2-(2,3,4,6-tetra-О-acetyl-β-d-glucopyranosyloxy)benzyl bromide 
• 122186-40-7 2-(2,3,4,6-tetra-O-acetyl-β-_D-glucopyranozyloxy)benzyl alcohol 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 

Downstream Products

• 60523-66-2 2-(2,3,4,6-tetra-О-acetyl-β-d-glucopyranosyloxy)benzyl bromide 
• 7234-31-3 o-tolyl-β-D-glucopyranoside 
• 115431-91-9 (2R,3R,4S,5R,6S)-3,4,5-Trimethoxy-2-methoxymethyl-6-(2-methyl-cyclohexa-1,4-dienyloxy)-tetrahydro-pyran 
• 115431-89-5 (2R,3R,4S,5R,6S)-3,4,5-Trimethoxy-2-methoxymethyl-6-o-tolyloxy-tetrahydro-pyran 
• 161767-44-8 2-(bromomethyl)phenyl tetra-O-acetyl-α-D-glucopyranoside 
• 7234-31-3 o-tolyl-α-D-glucopyranoside 
• 161767-40-4 2-(fluoromethyl)phenyl α-D-glucopyranoside 
• 143836-12-8 2-bromomethyl-4-nitrophenyl tetra-O-acetyl-α-D-glucopyranoside 
• 143836-13-9 2-chloromethyl-4-nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside 
• 143836-10-6 2-chloromethyl-4-nitrophenyl α-D-glucopyranoside 
• 161767-45-9 2-(chloromethyl)phenyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside 
• 143836-15-1 2-(chloromethyl)phenyl α-D-glucopyranoside 
• 161767-48-2 2-methyl-6-nitrophenyl tetra-O-acetyl-α-D-glucopyranoside 
• 143836-11-7 2-methyl-4-nitrophenyl tetra-O-acetyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

Selective demethylation ofO-aryl glycosides by iridium-catalyzed hydrosilylation

The cleavage of alkyl ethers by hydrosilylation is a powerful synthetic tool for the generation of silyl ethers. Previous attempts to apply this transformation to carbohydrate derivatives have been constrained by poor selectivity and preferential reductio

CHELATION CONTROLLED REGIOSELECTIVE ALKYLATION AND 1,4 CHIRALITY TRANSFER IN OPTICALLY ACTIVE 1-ALKOXY-1,4-CYCLOHEXADIENES

Chelation controlled alkylation of optically active 1-alkoxy-1,4-cyclohexadienes leads to a mixture of 1,4-cyclohexadienes 4a-c and 1,3-cyclohexadienes 5a-c.The regio- and diastereoselectivities depend upon the nature of the chiral auxiliary and the react