20231-38-3

Upstream product

• 3162-96-7 methyl 4,6-O-benzylidene-α-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 7177-79-9 methyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 

Downstream Products

• 37116-67-9 methyl-(O²,O³-dibenzyl-O⁴-methyl-O⁶-trityl-α-D-glucopyranoside) 
• 87326-58-7 methyl 4-O-allyl-2,3-di-O-benzyl-6-O-trityl-α-D-glucopyranoside 
• 81255-12-1 methyl 2,3-di-O-benzyl-6-O-triphenylmethyl-α-D-xylo-hexopyranosid-4-ulose 
• 162191-08-4 Methyl 2,3-di-O-benzyl-4-O-methyloxalyl-6-O-triphenylmethyl-α-D-glucopyranoside 
• 162191-07-3 Methyl 2,3-di-O-benzyl-4-O-(p-fluorophenoxy)-thionocarbonyl-6-O-triphenylmethyl-α-D-glucopyranoside 
• 19877-37-3 Methyl 2,3-di-O-benzyl-4-O-methanesulfonyl-6-O-triphenylmethyl-α-D-glucopyranoside 
• 162191-06-2 Methyl 2,3-di-O-benzyl-4-O-(phenoxy)-thionocarbonyl-6-O-triphenylmethyl-α-D-glucopyranoside 
• 162191-09-5 Methyl 2,3-di-O-benzyl-4-deoxy-6-O-triphenylmethyl-α-D-xylo-hexopyranoside 
• 17791-36-5 methyl 2,3-di-O-benzyl-α-D-glucopyranoside 
• 116013-34-4 (2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate 
• 87326-47-4 methyl 4-O-benzoyl-2,3-di-O-benzyl-α-D-glucopyranoside 
• 71756-38-2 methyl 2,3-di-O-benzyl-6-O-trityl-α-D-galactopyranoside 
• 81255-14-3 methyl 2,3-di-O-benzyl-4-C-methyl-α-D-glucopyranoside 
• 81255-13-2 methyl 2,3-di-O-benzyl-4-C-methyl-6-O-triphenylmethyl-α-D-glucopyranoside 

Relevant academic research and scientific papers

3-Butenyloxycarbonyl as a new hydroxyl protecting group in carbohydrate synthesis

3-Butenyloxycarbonyl (Bloc) has been identified as a new hydroxyl protecting group, which can be introduced under mild conditions in high yields and selectively removed by OsO4/NaIO4/2,6-lutidine in CH3CN-H2O wi

Intramolecular base-free sonogashira reaction for the synthesis of benzannulated chiral macrocycles embedded in carbohydrate templates

A base-free, intramolecular Sonogashira reaction-based general approach has been established for the diversity-oriented synthesis (DOS) of fused bi- and tricyclic systems containing benzannulated, 10- to 13-membered chiral macrocycles embedded in carbohydrate templates. Macrocycles with different ring sizes have been prepared by pre-designing the chiral building blocks. Base-sensitive groups like acetyl and TBDPS survived the reaction conditions. Copyright

Disaccharide-containing macrocycles by click chemistry and intramolecular glycosylation

In this study o- and m-xylylene moieties in combination with a triazolylmethyl moiety have been successfully employed as a relatively rigid spacer system in intramolecular glycosylation reactions. Phenyl 3,4,6-tri-O-benzyl-2-O-propargyl-1-thio-D-glucopyra