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

abysmal

不滿分子

Facile Hydrogenation of Acenapthylenes and Azulenes on the Face of a Triruthenium Carbonyl Moiety: D hydrogenative cluster fragmentation to mononuclear ruthenium hydrides; the stereochemistry of these complexes suggests that the reaction takes place through the activation of H. by the multinuclear species. The roles of the acenaphthylene or azulene ligands as hemilabile μ.-ligands for triruthenium

glomeruli

Mechanism of the Nickel-Catalyzed Electrosynthesis of Ketones by Heterocoupling of Acyl and Benzyl HCOCH.Ph is prevented because of the too slow oxidative addition of Ni.(.) to PhCH.COCl compared to PhCH.Br. The formation of the homocoupling product PhCH.CH.Ph is also prevented because PhCH.Ni.(.). does not react with PhCH.Br. This explains why the electrosynthesis of the ketone can be performed s

即席演說

wall-stress

織物

defenses

卷發(fā)

Patrícia Pinto,Maria J. Calhorda,Vitor Félix,Teresa Avilés,Michael G. B. Drew

送秋波

Felipe Gómez-de la Torre,Yolanda Gutiérrez,Félix A. Jalón,Blanca R. Manzano,Ana Rodríguez

Gnrh670