Parekh, Vimal’s team published research in Tetrahedron: Asymmetry in 2010-06-23 | 1192620-83-9

Tetrahedron: Asymmetry published new progress about Enantioselective synthesis. 1192620-83-9 belongs to class amides-buliding-blocks, and the molecular formula is C30H31ClN2O2RuS, Recommanded Product: Chloro[N-[(1R,2R)-1,2-diphenyl-2-[[3-(η6-phenyl)propyl]amino-κN]ethyl]-4-methylbenzenesulfonamidato-κN]ruthenium.

Parekh, Vimal; Ramsden, James A.; Wills, Martin published the artcile< Asymmetric transfer hydrogenation of quinolines using tethered Ru(II) catalysts>, Recommanded Product: Chloro[N-[(1R,2R)-1,2-diphenyl-2-[[3-(η6-phenyl)propyl]amino-κN]ethyl]-4-methylbenzenesulfonamidato-κN]ruthenium, the main research area is asym transfer hydrogenation quinoline ruthenium catalyst.

The first report of an asym. transfer hydrogenation, in formic acid/triethylamine, of quinolines is described. Using a Ru(II) catalyst containing a 4-carbon tether, products of up to 73% ee were formed, while a Rh(III)-tethered catalyst gave products of up to 94% ee.

Tetrahedron: Asymmetry published new progress about Enantioselective synthesis. 1192620-83-9 belongs to class amides-buliding-blocks, and the molecular formula is C30H31ClN2O2RuS, Recommanded Product: Chloro[N-[(1R,2R)-1,2-diphenyl-2-[[3-(η6-phenyl)propyl]amino-κN]ethyl]-4-methylbenzenesulfonamidato-κN]ruthenium.

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics