736151-93-2

Upstream product

• 32315-10-9 bis(trichloromethyl) carbonate 
• 81477-94-3 N-(diphenylmethylene)glycine tert-butyl ester 
• 115276-75-0 ethyl (E)-2-(p-methoxyphenylimino)acetate 

Downstream Products

• 736151-95-4 tert-butyl (4S,5S,1'S)-5-(1'-cyanohydroxymethyl)-1-(4-methoxyphenyl)-2-oxoimidazolidine-4-carboxylate 
• 736152-12-8 tert-butyl (4S,5S,1'R)-5-(1'-cyanohydroxymethyl)-1-(4-methoxyphenyl)-2-oxoimidazolidine-4-carboxylate 
• 736152-21-9 tert-butyl (4S,5S)-5-(2'-N-(tert-butoxycarbonyl)-N-(4-methoxybenzyl)aminoacetyl)-1-(4-methoxyphenyl)-2-oxoimidazolidine-4-carboxylate 
• 736152-19-5 tert-butyl (4S,5S,1'S)-5-(2'-N-(tert-butoxycarbonyl)-N-(4-methoxybenzyl)amino-1'-hydroxyethyl)-1-(4-methoxyphenyl)-2-oxoimidazolidine-4-carboxylate 
• 736152-02-6 tert-butyl (4S,5S,1'R)-5-(2'-N-(tert-butoxycarbonyl)-N-(4-methoxybenzyl)amino-1'-hydroxyethyl)-1-(4-methoxyphenyl)-2-oxoimidazolidine-4-carboxylate 
• 736152-17-3 tert-butyl (4S,5S,1'S)-5-(2'-N-(4-methoxybenzyl)amino-1'-hydroxyethyl)-1-(4-methoxyphenyl)-2-oxoimidazolidine-4-carboxylate 
• 736152-00-4 tert-butyl (4S,5S,1'R)-5-(2'-N-(4-methoxybenzyl)amino-1'-hydroxyethyl)-1-(4-methoxyphenyl)-2-oxoimidazolidine-4-carboxylate 
• 736151-90-9 (3aS,7R,7aS)-7-Hydroxy-5-(4-methoxy-benzyl)-1-(4-methoxy-phenyl)-hexahydro-imidazo[4,5-c]pyridine-2,4-dione 
• 736152-15-1 tert-butyl (4S,5S,1'S)-5-(2'-amino-1'-hydroxyethyl)-1-(4-methoxyphenyl)-2-oxoimidazolidine-4-carboxylate 
• 736151-97-6 tert-butyl (4S,5S,1'R)-5-(2'-amino-1'-hydroxyethyl)-1-(4-methoxyphenyl)-2-oxoimidazolidine-4-carboxylate 

Relevant academic research and scientific papers

Catalytic asymmetric synthesis of a nitrogen analogue of dialkyl tartrate by direct mannich reaction under phase-transfer conditions

(Equation Presented) Phase-transfer-catalyzed direct Mannich reaction of glycinate Schiff base 3 with α-imino ester 4 has been accomplished with high enantioselectivity by the utilization of N-spiro C2-symmetric chiral quaternary ammonium bromi