作者: Charles J. Weiss , Tobin J. Marks
DOI: 10.1039/C003089A
关键词: Combinatorial chemistry 、 Catalysis 、 Organic chemistry 、 Alkyne 、 Transition metal 、 Highly selective 、 Homogeneous catalysis 、 Reactivity (chemistry) 、 Chemistry 、 Lanthanide 、 Hydroalkoxylation
摘要: Lanthanide and actinide catalysts have made significant contributions to many areas of homogeneous catalysis with hydroelementation C–C unsaturation being a notable area success. In this Perspective, we review recent advances in f-element for highly selective hydroalkoxylation hydrothiolation processes. As will be discussed, exhibit selectivities unobtainable by late transition metal complexes. First, lanthanide-mediated processes mechanistic, thermodynamic, kinetic considerations then compare/contrast them analogous C–N C–P bond-forming transformations. addition, computational studies are discussed which provide further insight into transformation the observed selectivities. Next, actinide-mediated alkyne is reviewed similar discussion reactivity, mechanism, thermodynamics.