212892-11-0

Upstream product

• 212892-09-6 {(R)-1-[(4R,5S)-5-((R)-1,2-Dihydroxy-ethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-trityloxy-ethyl}-carbamic acid tert-butyl ester 
• 126199-70-0 [(R)-1-((4R,5R)-5-Acryloyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-trityloxy-ethyl]-carbamic acid tert-butyl ester 
• 124665-84-5 (3R,4R,5R)-1-(tert-butoxycarbonyl)-3,4-isopropylidenedioxy-5-trityloxymethyl-2-pyrrolidinone 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 212892-50-7 (2R,3R,4S,5S)-N-tert-butoxycarbonyl-3,4-isopropylidenedioxy-2-trityloxymethyl-5-hydroxymethylpyrrolidine 
• 212892-46-1 ((R)-1-{(4R,5S)-5-[(R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-[1,3]dioxolan-4-yl}-2-trityloxy-ethyl)-carbamic acid tert-butyl ester 

Downstream Products

• 212892-38-1 (3aS,4S,6R,6aR)-4-((R)-1-Methoxymethoxy-but-3-enyl)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylic acid tert-butyl ester 
• 212892-32-5 (3aS,4S,6R,6aR)-4-((S)-1-Methoxymethoxy-but-3-enyl)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylic acid tert-butyl ester 
• 212892-30-3 (2R,3R,4S,5S)-N-tert-butoxycarbonyl-3,4-isopropylidenedioxy-2-trityloxymethyl-5-((1S)-1-hydroxy-3-butenyl)pyrrolidine 
• 212892-36-9 (2R,3R,4S,5S)-N-tert-butoxycarbonyl-3,4-isopropylidenedioxy-2-trityloxymethyl-5-((1R)-1-hydroxy-3-butenyl)pyrrolidine 
• 704901-95-1 tert-butyl (3aR,4R,6S,6aS)-4-[(benzylamino)methyl]-6-{{[(tert-butyl)dimethylsilyl]oxy}methyl}tetrahydro-2,2-dimethyl-5H-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylate 
• 212892-50-7 (2R,3R,4S,5S)-N-tert-butoxycarbonyl-3,4-isopropylidenedioxy-2-trityloxymethyl-5-hydroxymethylpyrrolidine 

Relevant academic research and scientific papers

Syntheses and Glycosidase Inhibitory Activities of 2-(Aminomethyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol Derivatives

New 2-(aminomethyl)-5-(hydroxymethyl)pyrrolidine-3,4-diol derivatives were synthesized from (5S)-5-[(trityloxy)methyl]pyrrolidin-2-one (6) (Schemes 1 and 2) and their inhibitory activities toward 25 glycosidases assayed (Table). The influence of the confi

Stereoselective synthesis of alexine stereoisomers from (S)- pyroglutamic acid

Four stereoisomers of alexine (1,7a-diepialexine (1a), 1,7,7a- triepialexine (1b), 1-epialexine (30a), and 1,7-diepialexine (30b)), the polyhydroxylaled pyrrolizidine alkaloid, were synthesized from (S)- pyroglutamic acid derivative (6).