773121-57-6Relevant articles and documents
Cobalt-Hydride-Catalyzed Hydrosilylation of 3-Alkynes Accompanying I-Bond Migration
Kim, Yeong Bum,Kim, Dongwook,Dighe, Shashikant U.,Chang, Sukbok,Park, Jung-Woo,Park, Jung-Woo
, p. 1548 - 1553 (2021)
We describe a protocol for cobalt-catalyzed hydrosilylation of 3-alkynes with accompanying I-bond migration. Mechanistic studies indicate that (i) cobalt(I)-hydride bearing a bulky bisphosphine ligand is the key intermediate and (ii) I-bond migration occurs prior to hydrosilylation. The cascade process selectively furnishes terminal branched allylsilanes under mild conditions.
Chemoselective ruthenium-catalyzed reduction of acid chlorides to aldehydes with dimethylphenylsilane
Gutsulyak, Dmitry V.,Nikonov, Georgii I.
supporting information; experimental part, p. 607 - 611 (2012/04/23)
A variety of aromatic and alkyl acid chlorides can be selectively converted into aldehydes using dimethylphenyl silane (HSiMe2Ph) as the reducing reagent in the presence of the cationic ruthenium catalyst {Cp[(i-Pr)3P]Ru(NCMe)2}+ [PF6] -. The reactions proceed under very mild conditions and are tolerant to many functional groups. Copyright