106989-73-5

Upstream product

• 64-17-5 ethanol 
• 32142-34-0 1-phenyl-2-(phenylamino)propane-1-one 
• 542-11-0 aniline hydrobromide 
• 23022-83-5 1-bromo-1-phenyl-2-propanone 
• 62-53-3 aniline 
• 2466-76-4 N-Acetylimidazole 
• 538-51-2 benzylidene phenylamine 
• 2114-00-3 2-bromo-1-phenyl-1-propanone 
• 1360876-62-5 N-methoxy-N-methyl-2-phenyl-2-(phenylamino)acetamide 
• 75-16-1 methylmagnesium bromide 
• 22065-57-2 ethyl 2-phenyldiazoacetate 
• 940866-95-5 ethyl N-phenyl-α-phenylglycinate 
• 22596-45-8 trans-2-methyl-2-nitro-3-phenyloxirane 
• 22596-45-8 2-methyl-2-nitro-3-phenyloxirane 

Downstream Products

• 10257-92-8 2-phenyl-3-methyl-1H-indole 
• 22920-59-8 N-(1-phenylpropyl)aniline 
• 41018-81-9 3,5-dimethyl-2-phenyl-1H-indole 
• 1360998-08-8 4-methyl-1,5-diphenyl-1H-imidazol-2-amine 

Relevant academic research and scientific papers

A three-component one-pot synthesis of penta-substituted pyrroles via ring opening of α-nitroepoxides

A novel and facile one-pot reaction has been developed to synthesize a variety of penta-substituted pyrroles from α-nitroepoxides, primary amines and dialkyl acetylenedicarboxylates under the conditions without catalyst. Furthermore, the controlled experi

Catalytic enantioselective synthesis of α-nitroepoxides via aminolytic kinetic resolution

The first enantioselective synthesis of β-aryl-substituted α-nitroepoxides, exploiting an organocatalyzed aminolytic kinetic resolution (AKR), has been developed. Ring-opening reaction of racemic α-nitroepoxides with aniline in the presence of a readily available Cinchona alkaloid-derived thiourea affords unreacted epoxides in up to 95% ee.

Titanium-mediated reductive cross-coupling reactions of imines with nitriles: An efficient route for the synthesis of α-aminoketones or 1,2-diketones

The reaction of imines with low-valent titanium species, generated in situ by using Ti(OiPr)4/2 c-C5H9MgCl reagent, affords titanium-imine complex, which can couple with nitriles to provide 2,5-diazatitanacyclop

Imidazole Derivatives Useful for Controlling Microbial Growth

Disclosure is provided for 1,4,5-substituted amino imidazole compounds useful to control microbial growth, compositions including these compounds, devices including these compounds, and methods of using the same.

A modular approach to the synthesis of 1,4,5-substituted-2-aminoimidazoles

Diversified 1,4,5-substituted-2-aminoimidazoles were rapidly assembled via sequential N-H insertion and Grignard addition to α-diazoesters. Lead compounds were identified as antibiotics against Gram-positive bacteria with an MIC value as low as 2 μg/mL.

Electroreductive Coupling of Aromatic Imines with Electrophiles in the Presence of Chlorotrimethylsilane

Electroreduction of aromatic imines in the presence of electrophiles gave the corresponding inter- and intramolecular coupling products when the reaction was carried out with the use of chlorotrimethylsilane (CTMS) as the trapping agent of an anion interm