1366087-99-1

Upstream product

• 88333-03-3 Benzyl isocyanide 
• 99-61-6 3-nitro-benzaldehyde 
• 98-16-8 3-trifluoromethylaniline 
• 76-03-9 trichloroacetic acid 

Downstream Products

• 1366088-11-0 3-benzyl-5-(m-nitrophenyl)-1-(m-trifluoromethylphenyl)imidazolidine-2,4-dione 
• 1366088-23-4 3-benzyl-5-(m-aminophenyl)-1-(m-trifluoromethylphenyl)imidazolidine-2,4-dione 
• 1366088-50-7 N-cyclohexyl 2-{N-(p-chlorophenoxyacetyl)-N-[3-(3-benzyl-2,4-dioxo-1-(m-trifluoromethylphenyl)imidazolidin-5-yl)phenylamino]}-2-(p-tolyl)acetamide 
• 1366088-52-9 N-cyclohexyl 2-{N-(p-nitrophenylacetyl)-N-[3-(3-benzyl-2,4-dioxo-1-(m-trifluoromethylphenyl)imidazolidin-5-yl)phenylamino]}-2-phenylacetamide 
• 1366088-56-3 N-cyclohexyl 2-{N-(3-phenylpropiolyl)-N-[3-(3-benzyl-2,4-dioxo-1-(m-trifluoromethylphenyl)imidazolidin-5-yl)phenylamino]}-2-(p-chlorophenyl)acetamide 

Relevant academic research and scientific papers

A diastereoselective synthesis of pseudopeptidic hydantoins by an Ugi/cyclization/Ugi sequence

A diastereoselective synthesis of helix-forming pseudopeptidic hydantoins by an Ugi 4CC/cyclization/reduction/Ugi 4CC sequence of reactions, giving mainly the l-adduct when benzoic acids were used, is described.