204776-67-0

Upstream product

• 35781-78-3 5,6-anhydro-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 204776-61-4 (3aR,5R,6S,6aR)-6-Benzyloxy-5-[(R)-1-benzyloxy-2-(4-methoxy-phenyl)-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole 
• 204776-63-6 (2R,3R,4R)-2,4-Bis-benzyloxy-5-(4-methoxy-phenyl)-pentane-1,3-diol 
• 204776-60-3 (R)-1-[(3aR,5R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-(4-methoxyphenyl)ethanol 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 100-39-0 benzyl bromide 
• 204776-65-8 Acetic acid (1R,2R)-2-benzyloxy-1-[(R)-1-benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-3-(4-methoxy-phenyl)-propyl ester 

Relevant academic research and scientific papers

Transformation of D-glucose to 1-deoxy-1-[4'-methoxyphenyl]-2R,3R,4R- pentitol template: Synthesis of Karalicin analogues

Transformation of D-glucose to Karalicin isomers 1-1b is reported via the key chiron 5,6-anhydro-D-glucofuranose 2. Crucial protection and deprotection strategies of pentitol chiral template 6 are described.