164736-96-3

Upstream product

• 64-04-0 phenethylamine 
• 164736-93-0 (3R,4R)-3,4-dihydroxy-1-(2-phenylethyl)-2,5-pyrrolidinedione 

Downstream Products

• 2826-79-1 (+)-(10bR)-1,2,3,5,6,10b-Hexahydropyrrolo-<2,1-a>isoquinoline 
• 524950-96-7 (1S,2R,10bS)-1-benzoyloxy-2-(tert-butyldimethylsilanyloxy)-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinolin-3-one 
• 524950-98-9 (1S,2S,10bS)-2-benzoyloxy-1-hydroxy-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinolin-3-one 
• 524950-93-4 (1R,2R,10bS)-1-benzoyloxy-2-hydroxy-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinolin-3-one 
• 524950-97-8 (1S,2R,10bS)-1-benzoyloxy-2-hydroxy-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinolin-3-one 
• 524950-99-0 (1S,2S,10bS)-1-benzoyloxy-2-hydroxy-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinolin-3-one 
• 524950-94-5 (1R,2R,10bS)-1,2-dihydroxy-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinolin-3-one 
• 524950-87-6 (1S,2S,10bS)-1,2-dihydroxy-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinolin-3-one 
• 524950-92-3 (1S,2R,10bS)-2-benzoyloxy-1-hydroxy-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinolin-3-one 

Relevant academic research and scientific papers

Stereoselective synthesis of an isoquinolinopyrrolidinone by acyliminium ion cyclization of chiral hydroxylactams

Studies on the stereoselective synthesis of a pyrrolidinoisoquinoline derivative using acyliminium ion cyclization of hydroxylactams are described. Cyclization reaction of chiral hydroxylactams 2a~c, derived from (L)-tartaric acid and phenethylamine, affo

Synthesis of enantiopure 1,2-dihydroxyhexahydropyrroloisoquinolines as potential tools for asymmetric catalysis

The stereocontrolled synthesis of enantiopure 1,2-dihydroxyhexahydropyrroloisoquinolines 2-4 and a formal synthesis of ent-2-4 starting from D-mannose and L-tartaric acid is reported. The strong tertiary amine bases 2-4 containing hydroxyl groups, able to