362658-07-9

Upstream product

• 501-53-1 benzyl chloroformate 
• 362657-99-6 (2S,3S,4R,5R)-1-benzyloxycarbonyl-2-(1',2'-dihydroxyethyl)-3,4-isopropylidenedioxy-5-methylpyrrolidine 
• 362657-95-2 (2S,3S,4R,5R)-1-benzyl-2-(1',2'-dihydroxyethyl)-3,4-isopropylidenedioxy-5-methylpyrrolidine 
• 362657-58-7 (2S,3S,4R,5R)-1-benzyl-3,4-isopropylidenedioxy-5-methyl-2-vinylpyrrolidine 
• 362657-97-4 (2S,3S,4R,5R)-2-(1',2'-dihydroxyethyl)-3,4-isopropylidenedioxy-5-methylpyrrolidine 
• 188242-67-3 2,5-(benzyloxycarbonylimino)-3,4-O-isopropylidene-2,5,6-trideoxy-D-allose 

Downstream Products

• 362658-14-8 (2R,3S,4R,5R)-1-benzyloxycarbonyl-3,4-isopropylidenedioxy-5-methylproline methyl ester 

Relevant academic research and scientific papers

Synthesis of novel pyrrolidine 3,4-diol derivatives as inhibitors of α-L-fucosidases

The stereoselective synthesis of new 3,4-dihydroxypyrrolidine derivatives starting from D-mannose, D-ribose and L-fucose is presented. Two synthetic strategies employing organometallic addition to hemiacetalic sugars followed by selective nucleophilic dis

Stereoselective synthesis of (2S,3S,4R,5S)-5-methylpyrrolidine-3,4-diol derivatives that are highly selective α-L-fucosidase inhibitors

N-Phenylaminomethyl benzimidazolyl moieties attached at C-2 of (2S,3S,4R,5S)-5-methylpyrrolidine-3,4-diol increase the potency and selectivity of the inhibitory activity of these systems towards α-L-fucosidases. The Royal Society of Chemistry 2005.

Preparation and biological evaluation of pyrrolidinediols and pyrrolidine N-oxides from D-ribose using the nitrone approach

The transformation of 3,4-isopropylidenedioxy-5-methylpyrrolidine 1-oxides with various 2-substituents into the free diols and, by reduction, into the corresponding pyrrolidinediols (iminoglycitols) is described. The pyrrolidine N-oxides were derived from