This review covers the recent advances in hydrosilylation chemistry mainly published in the last decade. Hydrosilylation of olefins is an important reaction for the production of various organosilicon compounds such as industrially important silicone products. Although the utility of platinum catalysts, Speier's and Karstedt's catalysts, has been widely recognized in this field for decades, development of more efficient, selective, and cheaper catalyst systems are still desired for more economical production of organosilicon materials having superior properties. In these contexts, much progress has been made in recent years. In the platinum catalysis systems, continuous progress has been made to further improve selectivity and activity. Several non-precious metal catalysts, such as Fe and Ni catalysts, with good efficiency and selectivity have been developed. Furthermore, unique chemo- and regioselectivity have been achieved not only by precious metal catalysts but also by non-precious metal catalysts. The utility of non-transition metal catalysts including early main group metals, Lewis acidic alane, borane and phosphonium salts as well as N-heterocyclic carbenes has also been disclosed.

Mixed-acid systems consisting of both Lewis and Brønsted acids were found to be efficient catalysts for direct synthesis of methyl levulinate from cellulose.

Formally hexavalent palladium complexes have been isolated and structurally characterized for the first time. Thermal condensation reaction of three molecules of 1,2-C ₆ H ₄ (SiH ₂ ) ₂ Pd ^II (R ₂ PCH ₂ CH ₂ PR ₂ ) (where R is defined as a methyl or ethyl) provided trinuclear palladium complexes. Single-crystal x-ray analysis revealed that each of the central palladium atoms of the complexes is ligated by six silicon atoms and is hexavalent, whereas the other palladium atoms are divalent.