385797-51-3

Upstream product

• 1356003-46-7 1-acetyl-2-(benzylsulfanyl)-4,5-dihydro-1H-imidazol-4-one 
• 123-11-5 4-methoxy-benzaldehyde 
• 1356003-59-2 2-(benzylsulfanyl)-4,5-dihydro-1H-imidazol-4-one 
• 1356003-48-9 2-(benzylsulfanyl)-1-tert-butoxycarbonyl-4,5-dihydro-1H-imidazol-4-one 
• 95474-45-6 5-p-methoxybenzylidene-2-thiohydantoin 
• 100-39-0 benzyl bromide 

Downstream Products

• 1356003-65-0 (Z)?5?(4?methoxybenzylidene)?2?(4?methoxyphenyl)?3,5?dihydro?4H?imidazol?4?one 
• 1356003-64-9 (4Z)-2-(benzylsulfanyl)-1-(4-methoxybenzyl)-4-(4-methoxybenzylidene)-4,5-dihydro-1H-imidazol-5-one 
• 1356003-61-6 (5Z)-2-(benzylsulfanyl)-3-tert-butoxycarbonyl-5-(4-methoxybenzylidene)-4,5-dihydro-1H-imidazol-4-one 
• 1356003-63-8 (4Z)-1-benzyl-2-(benzylsulfanyl)-4-(4-methoxybenzylidene)-4,5-dihydro-1H-imidazol-5-one 
• 1356003-68-3 (4Z)-1-benzyl-4-(4-methoxybenzylidene)-2-(4-methoxyphenyl)-4,5-dihydro-1H-imidazol-5-one 
• 1356003-62-7 (5Z)-3-benzyloxycarbonyl-2-(benzylsulfanyl)-5-(4-methoxybenzylidene)-4,5-dihydro-1H-imidazol-4-one 
• 1356003-67-2 (4Z)-1-benzyloxycarbonyl-4-(4-methoxybenzylidene)-2-(4-methoxyphenyl)-4,5-dihydro-1H-imidazol-5-one 

Relevant academic research and scientific papers

Thiohydantoins: Selective N- and S-functionalization for Liebeskind-Srogl reaction study

Thiohydantoins formed by the Schlack-Kumpf protocol were selectively functionalized at the nitrogen, sulfur, or carbon atom to test the Liebeskind-Srogl reaction possibilities. Georg Thieme Verlag Stuttgart. New York.