“…[1,2] The seminal discoveries of the very high efficiency of the hydrogenation of olefins by Au 0 in the early 1970s, [3] and of the addition of a C nucleophile to a carbonyl moiety catalyzed by a Au I complex in 1986, [4] truly launched these two parallel research domains. Since then, focusing only on homogeneous processes, very efficient and selective processes have been devised, including hydrogenation, [5] hydrosilylation, [6] or nucleophilic additions to p-systems. [1,4,7] Recently, the dehydrogenative silylation of alcohols using Au I chloride complexes was reported by Ito et al [8] In the above-mentioned processes involving "H-Y" (Y = H, BR 2 , SiR 3 ) reagents, Au À H intermediates have been postulated [5c-e, 6a, 8] in direct analogy with the same processes using other transition metals for which such M À H bonds have been observed and fully characterized.…”