176718-64-2

Upstream product

• 501-53-1 benzyl chloroformate 
• 149342-28-9 1,4-Dideoxy-1,4-imino-2,3-di-O-isopropylidene-5-O-trityl-l-lyxitol 

Downstream Products

• 176718-67-5 (2S,3R,4S)-4-(tert-Butyl-dimethyl-silanyloxy)-3-methoxymethoxy-2-trityloxymethyl-pyrrolidine-1-carboxylic acid benzyl ester 
• 176718-65-3 (2S,3R,4S)-4-(tert-Butyl-dimethyl-silanyloxy)-3-hydroxy-2-trityloxymethyl-pyrrolidine-1-carboxylic acid benzyl ester 
• 176718-68-6 (2S,3R,4S)-N-benzyloxycarbonyl-4-hydroxy-3-methoxymethyloxy-2-trityloxymethylpyrrolidine 
• 129492-78-0 (2S,3R,4S)-N-benzyloxycarbonyl-3,4-dihydroxy-2-hydroxymethylpyrrolidine 

Relevant academic research and scientific papers

Synthesis of 1,4-imino-L-lyxitols modified at C-5 and their evaluation as inhibitors of GH38 α-mannosidases

A synthetic approach to 1,4-imino-L-lyxitols with various modifications at the C-5 position is reported. These imino-L-lyxitol cores were used for the preparation of a series of N-(4-halobenzyl)polyhydroxypyrrolidines. An impact of the C-5 modification on

Chiral pyrrolidine derivatives as catalysts for the enantioselective addition of diethylzinc to aldehydes

A chiral hydroxylated pyrrolidine derivative (4) and an N-(2- mercaptoethyl)pyrrolidine derivative (1c) were synthesized from D- ribonolactone and were used as chiral catalyst ligands in the reaction of diethylzinc and aldehydes. High asymmetric induction