1435780-53-2

Upstream product

• 98-88-4 benzoyl chloride 
• 7464-56-4 1-O-allyl-α-D-glucopyranoside 
• 492-62-6 alpha-D-glucopyranose 

Downstream Products

• 1435780-86-1 (S)-2-acetamido-3-(4-(α-D-tetra-O-benzoylglucosyloxy)-(E)-but-2-enyloxy)propanoate benzyl ester 
• 1435780-90-7 (S)-2-acetamido-N-methyl-3-(4-(α-D-tetra-O-benzoylglucosyloxy)butoxy)propanamide 
• 1435781-02-4 (R)-2-acetamido-3-(4-(α-D-tetra-O-benzoylglucosyloxy)-(E)-but-2-enylthio)propanoate benzyl ester 
• 1435781-06-8 (R)-2-acetamido-N-methyl-3-(4-(α-D-tetra-O-benzoylglucosyloxy)butylthio)propanamide 
• 1435780-82-7 (S)-2-(tert-butoxycarbonylamino)-3-(4-(α-D-tetra-O-benzoylglucosyloxy)-(E)-but-2-enyloxy)propanoate benzyl ester 
• 1435780-98-5 (R)-2-(tert-butoxycarbonylamino)-3-(4-(α-D-tetra-O-benzoylglucosyloxy)-(E)-but-2-enylthio)propanoate benzyl ester 
• 6605-40-9 methyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 
• 149707-75-5 2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl trichloroacetimidate 

Relevant academic research and scientific papers

Carbon tetrachloride-free allylic halogenation-mediated glycosylations of allyl glycosides

The allylic bromination of allyl glycosides is conducted using NBS/AIBN reagents in (EtO)2CO and PhCF3 solutions, without using CCl4 as a solvent. The activated mixed halo-allyl glycosides led to glycosylations, mediated by a triflate, in a latent-active

Synthesis and conformational analysis of neoglycoconjugates derived from O- and S-glucose

Using olefin metathesis as a key step, four neoglycoconjugates incorporating α-O-glucose, α-S-glucose or β-S-glucose as a carbohydrate unit and l-serine or l-cysteine as an amino acid moiety have been synthesized. The four-atom carbon spacer allows the carbohydrate to explore a wide-ranging conformational space, which may have important implications for the molecular recognition of these molecules.