125629-92-7

Upstream product

• 100-39-0 benzyl bromide 
• 17342-08-4 (S)-Pyroglutaminol 
• 125629-91-6 (S)-5-(hydroxymethyl)-1-(phenylmethyl)-2-pyrrolidinone 
• 38854-94-3 N-benzyl-L-pyroglutamic acid 
• 103301-78-6 methyl (2S)-1-benzyl-5-pyrrolidone-2-carboxylate 

Downstream Products

• 113571-63-4 (3R,4R,5R)-1-benzyl-5-benzyloxymethyl-3,4-dihydroxy-2-pyrrolidinone 
• 113571-62-3 (3S,4S,5R)-1-benzyl-5-benzyloxymethyl-3,4-dihydroxy-2-pyrrolidinone 
• 132489-30-6 (3S,4S,5R)-1-benzyl-5-benzyloxymethyl-3,4-isopropylidenedioxy-2-pyrrolidinone 
• 113571-61-2 (S)-1-benzyl-5-benzyloxymethyl-2-oxo-3-pyrroline 
• 113571-59-8 (2R,3S,4R)-N-benzyl-2-hydroxymethyl-3,4-O-isopropylidenepyrrolidine-3,4-diol 
• 72741-87-8 swainsonine 

Relevant academic research and scientific papers

An efficient, enantioselective synthesis of branched polyhydroxylated pyrrolidines

The enantioselective synthesis of branched polyhydroxylated pyrrolidines from a novel α-methylene bicyclic lactam (4b) is described. (C) 2000 Elsevier Science Ltd.

Diastereoselective alkylation of 1-benzyl-(5S)-substituted 2-pyrrolidinones

The (S)-glutamic acid derivatives, (5S)-methoxymethyl- and (5S)-benzyloxymethyl N-benzyl-2-pyrrolidinones, compounds 3a and 3b respectively, exhibit good to excellent diastereoselection upon alkylation with primary alkyl bromides or iodides.