Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kai Y. Wan"'
Publikováno v:
Organometallics. 37:491-504
The imidazolium salt [(S,S)-tBuNC3H3NCHPhCHPhNH2]PF6, (S,S)-11·HPF6 is a precursor to the enantiopure “Kaibene” ligand, tBu-Kaibene, (S,S)-11 featuring a tert-butyl group on the N-heterocyclic carbene (NHC) ring-nitrogen atoms. It has been prepa
Publikováno v:
ACS Catalysis. 7:6827-6842
By using a copper transmetalation reagent [Cu(Kaibene)2]I, the NHC ligand (S,S)-MeNC3H2NCHPhCHPhNH2 “Kaibene” was transferred to ruthenium to make a precatalyst [RuCp*(Kaibene)(MeCN)](PF6) (Cp* = 1,2,3,4,5-pentamethylcyclopentadienyl), 7, in high
Publikováno v:
ACS Catalysis. 7:316-326
Our group previously reported the development of iron carbonyl catalysts bearing chiral tridentate P–N–P′ ligands for the asymmetric hydrogenation of prochiral ketones in THF. An NMR study into the activation process identified the amine hydrid
Publikováno v:
Organometallics. 35:1604-1612
By a simple SN2 reaction between N-methylimidazole and a chiral sulfamidate, the first proligand of a new class of enantiopure NHC-CHPh-CHPh-NH2 ligands can be prepared in high yield. This proligand, with the molecular formula [(S,S)-H2NCHPhCHPh-NC3H
Autor:
Kai Y. Wan, Paraskevi O. Lagaditis, Peter E. Sues, Alan J. Lough, Robert H. Morris, Jessica F. Sonnenberg
Publikováno v:
Journal of the American Chemical Society. 136:1367-1380
After their treatment with LiAlH4 and then alcohol, new iron dicarbonyl complexes mer-trans-[Fe(Br)(CO)2(P-CH═N-P')][BF4] (where P-CH═N-P' = R2PCH2CH═NCH2CH2PPh2 and R = Cy or iPr or P-CH═N-P' = (S,S)- Cy2PCH2CH═NCH(Me)CH(Ph)PPh2) are catal