Iron-Catalyzed Cyclization of Nitrones with Geminal-Substituted Vinyl Acetates: A Direct [4 + 2] Assembly Strategy Leading to 2,4-Disubstituted Quinolines
作者:Mingbing Zhong、Song Sun、Jiang Cheng、Ying Shao
DOI:10.1021/acs.joc.6b01910
日期:2016.11.18
An iron-catalyzed intermolecular [4 + 2] cyclization of arylnitrones with geminal-substituted vinyl acetates was developed for the synthesis of 2,4-disubstituted quinolines in moderate to good yields with good functional group compatibilities. Preliminary mechanistic studies suggest a plausible iron-catalyzed C–H activation process under external-oxidant-free conditions.
Simple and Clean Photo-induced Methylation of Heteroarenes with MeOH
作者:Wenbo Liu、Xiaobo Yang、Zhong-Zhen Zhou、Chao-Jun Li
DOI:10.1016/j.chempr.2017.03.009
日期:2017.5
Heteroarene methylation utilizing a cheap and safe methylation source without involving transition metals represents an important yet challenging objective. Here, a simple and clean catalyst-free protocol for the methylation of various heteroarenes (including six- and five-membered types) is described under light irradiation. This protocol employs cheap, readily available, and abundant MeOH as both
Cu(ii)-promoted three-component coupling sequence for the efficient synthesis of substituted quinolines
作者:Fuhong Xiao、Wen Chen、Yunfeng Liao、Guo-Jun Deng
DOI:10.1039/c2ob26484f
日期:——
The copper-promoted three-componentcouplingsequence for substituted quinoline formation from aldehydes, anilines and acetone is described. Various 2-arylquinolines were selectively obtained in good yields under mild conditions. The reaction tolerated a wide range of functionalities.
Sustainable synthesis of quinolines (pyridines) catalyzed by a cheap metal Mn(I)‐NN complex catalyst
作者:Huining Chai、Weiqiang Tan、Yuanyuan Lu、Guangyao Zhang、Jiping Ma
DOI:10.1002/aoc.5685
日期:2020.8
example of a bidentate phosphine‐free manganese(I)‐NN complex catalyst for the synthesis of quinolines (pyridines) through acceptorless dehydrogenative condensation of various secondary alcohols with amino alcohols. The coupling reactions occurred at 3 mol% catalyst loading and 110°C, and tolerated diverse functional groups. Moderate to excellent yields ranging from 45% to 89% were achieved after 12
Iridium compounds having at least two 2-arylpyridine ligands in which a non-hydrogen atom group is substituted at the 4-position of the pyridine ring, and light-emitting elements comprising on organic layer comprising at least one of the iridium compounds are disclosed.