581059-96-3

Upstream product

• 69622-40-8 2-(tert-butyl)-5-chloro-1H-indole 
• 3282-30-2 pivaloyl chloride 
• 65854-91-3 N-(4-chlorophenyl)-2,2-dimethylpropionamide 
• 1313017-13-8 N-[4-chloro-2-(2,2-dimethyl-1-oxopropyl)phenyl]-2,2-dimethylpropanamide 
• 880473-91-6 1-(5-chloro-2-nitrophenyl)-2,2-dimethylpropan-1-one 

Downstream Products

• 880473-88-1 N-[4-chloro-2-(2,2-dimethylpropionyl)phenyl]trifluoromethanesulfonamide 
• 1287718-36-8 (R(S))-N-(S)-[1-(2-amino-5-chlorophenyl)-2,2-dimethylpropyl]-2-methyl-2-propanesulfinamide 
• 1287838-42-9 (1S)-1-(2-amino-5-chlorophenyl)-2,2-dimethyl-1-propanamine 
• 1287838-45-2 (1S)-1-(2-amino-5-chlorophenyl)-N,2,2-trimethyl-1-propanamine 
• 1287718-19-7 N-[(Z)-1-(2-amino-5-chlorophenyl)-2,2-dimethylpropylidene]-2-methyl-(R(S))-2-propanesulfinamide 

Relevant academic research and scientific papers

2-Arylindoles: A new entry to transition metal-free synthesis of 2-aminobenzophenones

Various 2-aminobenzophenones were synthesized from readily available 2-arylindoles in DMSO under O2 balloon atmosphere. The synthesis was carried out without the aid of a transition metal catalyst or moisture-sensitive organometallic reagents from 2-arylindoles.

Asymmetric synthesis of 1,3-diamines. II: Diastereoselective reduction of atropisomeric N-tert -butanesulfinylketimines

Chiral, nonracemic o-aminobenzylamines were prepared in a highly diastereoselective reduction of atropisomeric N-tert-butanesulfinylketimines. The ortho-substituent ensures the distinct reactivity of atropisomers 4d-f. The free energy of activation for at

Control of parasites in animals by the use of novel trifluoromethanesulfonanilide oxime ether derivatives

Novel trifluoromethanesulfonanilide oxime ether compounds useful for controlling endo and/or ectoparasites in the environment are provided, together with methods of making the same, and methods of using the inventive compounds to treat parasite infestations in vivo or ex vivo.