950587-55-0Relevant academic research and scientific papers
Redox-triggered ruthenium-catalyzed remote C?H acylation with primary alcohols
Li, Gongqiang,Xia, Ji-Bao,Guo, Xiao,Wu, Yang
, p. 12987 - 12995 (2020)
Redox-triggered metal-catalyzed cross-coupling reactions from readily available alcohols provide a step economical means to synthesize ketones and related compounds. Prior examples for hydrogenative remote C(sp3)?H functionalization of olefins via a metal walking process featured external reducing agents. Here, we report a strategy for redox-triggered hydrogenative remote C(sp3)?H acylation of olefins with primary alcohols both as an acylating agent and a reductant, which is validated by the base-free 1,3-diketone synthesis. Mechanistic studies have confirmed that the reaction takes place via an aldehyde intermediate and a metal walking process.
Ruthenium hydride catalyzed regioselective addition of aldehydes to enones to give 1,3-diketones
Fukuyama, Takahide,Doi, Takashi,Minamino, Satoshi,Omura, Sohei,Ryu, Ilhyong
, p. 5559 - 5561 (2008/09/17)
(Chemical Equation Presented) It all adds up: Straightforward access to 2-alkyl-substituted 1,3-diketones is provided by a regioselective addition of aldehydes to enones catalyzed by the ruthenium hydride catalyst [RuHCl(CO)(PPh3)3]
