synthesis of N-methyl-3-chalcogeno-indoles has been developed via iodine-mediatedelectrophilicannulation reactions of 2-alkynylaniline derivatives with disulfides or diselenides. In the presence of iodine and iron, a variety of 2-alkynylanilines selectively underwent the electrophilicannulation with numerous disulfides or diselenides leading to the corresponding 3-sulfenylindoles and 3-selenenylindoles
Palladium-Catalyzed Synthesis of 2,3-Diaryl-<i>N</i>-methylindoles from <i>ortho</i>-Alkynylanilines and Aryl Pinacol Boronic Esters
作者:Yue-Gui Luo、R. Sidick Basha、Daggula Mallikarjuna Reddy、Yong-Jing Xue、Te-Hsuan Chen、Chin-Fa Lee
DOI:10.1021/acs.orglett.8b02835
日期:2018.11.2
A palladium-catalyzed synthesis of 2,3-diaryl-N-methylindoles from o-alkynylanilines and aryl pinacol boronic esters was developed. The system possesses high functional group tolerance and a broad substrate scope with a variety of aryl pinacol boronic esters to provide valuable 2,3-diaryl-N-methylindoles in moderate to good yields. Remarkably, the sequential reaction controlled by iridium-catalyzed
Palladium-catalyzed synthesis of 2,3-disubstituted indoles <i>via</i> arylation of <i>ortho</i>-alkynylanilines with arylsiloxanes
作者:Yang-Ting Hsia、Yu-Lin Lu、Rekha Bai、Satpal Singh Badsara、Chin-Fa Lee
DOI:10.1039/d3ob00961k
日期:——
study, we report the electrophiliccyclization of N,N-dimethyl-o-alkynylanilines with arylsiloxanes in the presence of [Pd(OAc)2] and Ag2O catalytic system, which leads to the efficient synthesis of indoles, similar to the one that is obtained through Larock indole synthesis. A range of aryl(trimethoxy)silanes with EDGs and EWGs were successfully utilized for the synthesis of a diverse variety of substituted
Au-promoted Pd-catalyzed arylative cyclization of N,N-dimethyl-o-alkynylaniline with aryl iodides: Access to 2,3-diaryl indoles and mechanistic insight
作者:Kemeng Yuan、Jiwei Wang、Feijun Wang、Jun Zhang
DOI:10.1016/j.tetlet.2020.152766
日期:2021.2
Application of FeCl3/Diorganyl Diselenides to Cyclization of o-Alkynyl Anilines: Synthesis of 3-Organoselenyl-(N-methyl)indoles
In this manuscript we described the FeCl3/diorganyl diselenides promoted intramolecular cyclization of o-alkynyl anilines, as an alternative for the construction of functionalized 3-organoselenyl indoles. The cyclization reactions proceeded smoothly at room temperature in the presence of air giving the 3-organoselenyl indoles in good yields. Additionally, the 3-organoselenyl indoles proved to be quite useful as synthetic intermediates for the construction of more functionalized indole units through a selenium-lithium exchange reaction followed by trapping the lithium intermediate with different electrophiles.