Titlebook: Organometallic Chemistry and Catalysis; Karl Kirchner,Walter Weissensteiner Book 2001 Springer-Verlag Wien 2001 Inorganic Chemistry.Organo

含水层

gnarled

绿州

Rhodium-Catalyzed Amination of Aromatic Olefinsamines. Styrene as the hydrogen acceptor gave concomitantly ethylbenzene. In the presence of 1,5-cyclooctadiene (.) preferential reduction to cyclooctene takes place. The addition of . reduces the rate of the reaction, but also the amount of ethylbenzene produced. Here, for the first time the ratio

躲债

neurologist

Iridium(I)-Catalyzed Asymmetric Intermolecular Hydroarylation of Norbornene with Benzamide′-dimethoxy-biphenyl-2,2′-diyl)-1,1′-.-(diphenylphosphine), and (.)-1 -((.)-2-(diphenylphosphino-ferrocenyl))-ethyldicyclohexyl-phosphine), a new class of cyclopentadienyl Ir(I) complexes containing a chiral bisphosphine ([Ir.(.)]) was prepared and characterized. These new complexes are suited preca

fender

Synthesis, Characterization, and Catalytic Activity of Rh(I) Complexes with (,)-,, an Axially Chiralenylphosphanyl)-l,l′-binaphtha-lene ((.)-., 1) leads to the formation of cationic complexes [(.)Rh(.)]. where the ligand (.)-. consistently displays a P,O-chelate coordination which is mantained even in solvents of fair polarity. The mononuclear rhodium(I) complexes (.)-2-diphenylphosphanyl-2′-diphe

Density

Enantioselective Catalyses CXXXV [1]. Stereoselective Hydrogenation of Folic Acid and 2-Methylquinoxat C6 of the pteridine system. With rhodium(I) catalysts of optically active phosphanes, which were immobilized on silical gel, the hydrogenation in aqueous solution can be controlled stereoselectively. The highest diastereomeric excess of .. 40% is obtained with (−)-.-containing catalysts. The hydr

投票

Formidable

https://doi.org/10.1007/978-3-7091-6274-3Inorganic Chemistry; Organometallic chemistry; Rearrangement; anorganische Chemie; catalysis; homogeneous

背带

Springer-Verlag Wien 2001