18213-90-6Relevant articles and documents
Ruthenium-catalysedmeta-selective CAr-H bond alkylationviaa deaminative strategy
Zhu, Ze-Fan,Chen, Guang-Le,Liu, Feng
supporting information, p. 3411 - 3414 (2021/04/07)
The use of aliphatic amines as alkylating reagents in organic synthesisviaC-N bond activation remains underdeveloped. We herein describe a novel ruthenium-catalysed and directing-group assisted protocol for the synthesis ofmeta-alkylated arenesviadual C-H and C-N activation. Bench-stable and easily handled redox-active Katritzky pyridinium salts derived from abundant amines and amino acid species were used as alkyl radical precursors. This catalytic reaction could accommodate a broad range of functional groups and provide access to variousmeta-alkylated products.
Aerobic copper-promoted oxidative dehydrosulfurative carbon-oxygen cross-coupling of 3,4-dihydropyrimidine-1: H -2-thiones with alcohols
Kwon, Yujeong,Lee, Dong-Chan,Lee, Jihong,Sohn, Jeong-Hun
, p. 36821 - 36825 (2021/12/02)
An aerobic Cu-promoted oxidative dehydrosulfurative carbon-oxygen cross-coupling of 3,4-dihydropyrimidin-1H-2-thiones (DHPMs) with both aliphatic and aromatic alcohols is described. Together with the ready availability of DHPMs and both alcohols, the meth
Synthesis of m-Alkylphenols via a Ruthenium-Catalyzed C-H Bond Functionalization of Phenol Derivatives
Li, Gang,Gao, Panpan,Lv, Xulu,Qu, Chen,Yan, Qingkai,Wang, Ya,Yang, Suling,Wang, Junjie
supporting information, p. 2682 - 2685 (2017/05/24)
The first example of the synthesis of m-alkylphenols via a ruthenium-catalyzed CAr-H bond functionalization of phenol derivatives with sec/tert-alkyl bromides is reported. Mechanistic studies indicated that the m-CAr-H bond alkylation may involve a radical process and that a six-membered ruthenacycle complex was the active catalyst. Moreover, this approach can provide an expedited strategy for the atom-/step-economical synthesis of many noteworthy pharmaceuticals and other functional molecules.
