Baratta, Walter; Barbato, Cinzia; Magnolia, Santo; Siega, Katia; Rigo, Pierluigi published the artcile< Chiral and Nonchiral [OsX2(diphosphane)(diamine)] (X: Cl, OCH2CF3) Complexes for Fast Hydrogenation of Carbonyl Compounds>, HPLC of Formula: 112-63-0, the main research area is osmium phosphino ferrocene diamine diphosphine complex preparation hydrogenation catalyst; ketone hydrogenation osmium phosphino ferrocene diamine diphosphine complex catalyst; aldehyde hydrogenation osmium phosphino ferrocene diamine diphosphine complex catalyst; enantioselective hydrogenation catalyst osmium diamine diphosphine complex.
The osmium complexes trans-[OsCl2(dppf)(diamine)] (dppf: 1,1′-bis(diphenylphosphino)ferrocene; diamine: ethylenediamine in 3, 1,3-propylenediamine in 4) were prepared by the reaction of [OsCl2(PPh3)3] (1) with the ferrocenyl diphosphine dppf and the corresponding diamine in dichloromethane. The reaction of derivative 3 with NaOCH2CF3 in toluene afforded the alkoxide cis-[Os(OCH2CF3)2(dppf)(ethylenediamine)] (5). The novel precursor [Os2Cl4(P(m-tolyl)3)5] (2) gave the chiral complexes trans-[OsCl2(diphosphine)(1,2-diamine)] (6-9; diphosphine: (R)-[6,6′-dimethoxy(1,1′-biphenyl)-2,2′-diyl]bis[1,1-bis(3,5-dimethylphenyl)phosphine] (xylMeObiphep) or (R)-(1,1′-binaphthalene)-2,2′-diylbis[1,1-bis(3,5-dimethylphenyl)phosphine] (xylbinap); diamine = (R,R)-1,2-diphenylethylenediamine (dpen) or (R,R)-1,2-diaminocyclohexane (dach)), obtained by the treatment of 2 with the diphosphine and the 1,2-diamine in toluene at reflux temperature Compounds 3-5 in ethanol and in the presence of NaOEt catalyze the reduction of Me aryl, dialkyl, and diaryl ketones and aldehydes with H2 at low pressure (5 atm), with substrate/catalyst (S/C) ratios of 10,000-200,000 and achieving turnover frequencies (TOFs) of up to 3.0 × 105 h-1 at 70°. By employment of the chiral compounds 6-9, different ketones, including alkyl aryl, bulky tert-Bu, and cyclic ketones, have successfully been hydrogenated with enantioselectivities up to 99% and with S/C ratios of 5000-100,000 and TOFs of up to 4.1 × 104 h-1 at 60°.
Chemistry – A European Journal published new progress about Alcohols Role: SPN (Synthetic Preparation), PREP (Preparation). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, HPLC of Formula: 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics