175792-75-3

Upstream product

• 155220-76-1 (S)-1-phenyl-2-benzylaminoethylamine 
• 5292-43-3 bromoacetic acid tert-butyl ester 
• 80-62-6 methacrylic acid methyl ester 
• 175792-71-9 (S)-1-benzyl-4-phenyl-4,5-dihydroimidazole 

Downstream Products

• 175793-15-4 (2S,4R)-1-benzyloxycarbonyl-2-(2-ethoxycarbonyl-(E)-ethenyl)-4-methoxycarbonyl-4-methylpyrrolidine 
• 175793-12-1 (2S,4R)-1-benzyloxycarbonyl-2-tert-butoxycarbonyl-4-methoxycarbonyl-4-methylpyrrolidine 
• 176739-83-6 (2S,4R)-1-benzyloxycarbonyl-4-methoxycarbonyl-4-methylpyrrolidine-2-carboxylic acid 
• 175793-13-2 (2S,4R)-1-benzyloxycarbonyl-2-hydroxymethyl-4-methoxycarbonyl-4-methylpyrrolidine 
• 175793-14-3 (2S,4R)-1-benzyloxycarbonyl-2-formyl-4-methoxycarbonyl-4-methylpyrrolidine 
• 175792-86-6 (2S,4R)-1-[(S)-2-benzylamino-1-phenylethyl]-2-tert-butoxycarbonyl-4-methoxycarbonyl-4-methylpyrrolidine 

Relevant academic research and scientific papers

Cycloaddition of homochiral dihydroimidazoles: A 1,3-dipolar cycloaddition route to optically active pyrrolo[1,2-a]imidazoles

N-Alkylation of optically active 1-benzyl-4-phenyl-4,5-dihydroimidazole with active alkyl halides and treatment of the so-formed 4,5-dihydroimidazolium ions with DBU in the presence of a range of electron-deficient alkene dipolarophiles, constitutes a 'on

Cycloaddition of homochiral imidazolinium ylides: A route to optically active pyrroloimidazoles

The synthesis of either enantiomer of 1-benzyl-4-phenyl-2-imidazoline from phenylglycine is described. 'One-pot' generation and enantioselective 1,3-dipolar cycloaddition of homochiral azomethine ylides prepared from these imidazolines with a range of alkene dipolarophiles affords optically active hexahydropyrroloimidazole adducts.