Organo-f-element catalysts for efficient and highly selective hydroalkoxylation and hydrothiolation

被引:198
作者
Weiss, Charles J. [1 ]
Marks, Tobin J. [1 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
关键词
BOND DISRUPTION ENTHALPIES; SATURATED OXYGEN HETEROCYCLES; FUNCTIONAL THEORY ANALYSIS; UNPROTECTED AMINO OLEFINS; TRIFLATE IONIC LIQUIDS; TERMINAL ALKYNES; INTRAMOLECULAR HYDROPHOSPHINATION/CYCLIZATION; INTERMOLECULAR HYDROAMINATION; RADICAL-ADDITION; ORGANOLANTHANIDE COMPLEXES;
D O I
10.1039/c003089a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Lanthanide and actinide catalysts have made significant contributions to many areas of homogeneous catalysis with hydroelementation of C-C unsaturation being a notable area of success. In this Perspective, we review recent advances in f-element hydroelementation for highly selective hydroalkoxylation and hydrothiolation processes. As will be discussed, f-element hydroalkoxylation and hydrothiolation catalysts exhibit selectivities unobtainable by many late transition metal complexes. First, we review lanthanide-mediated hydroalkoxylation processes with mechanistic, thermodynamic, and kinetic considerations discussed, and then compare/contrast them with analogous C-N and C-P bond-forming transformations. In addition, computational studies are discussed which provide further insight into this transformation and the observed selectivities. Next, actinide-mediated alkyne hydrothiolation is reviewed with a similar discussion of reactivity, mechanism, and thermodynamics.
引用
收藏
页码:6576 / 6588
页数:13
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