Synthesis of polyfunctional indoles and related heterocycles mediated by cesium and potassium bases
摘要:
A general preparation of 2-substituted indoles starting from functionalized 2-alkynylanilines has been developed. This base mediated reaction has also been used to synthesize the heterocyclic core of the marine alkaloid hinckdentine A. Furthermore the reaction was successfully adapted to the solid phase. Benzofurans and isoindolones could also be prepared with this method. (C) 2003 Elsevier Science Ltd. All rights reserved.
A concise approach for the synthesis of 3-iodoindoles and 3-iodobenzo[b]furans via Ph3P-catalyzed iodocyclization
作者:Yin-Long Li、Jian Li、Sheng-Nan Yu、Ji-Bo Wang、Yan-Min Yu、Jun Deng
DOI:10.1016/j.tet.2015.09.005
日期:2015.10
A variety of 3-iodoindole and 3-iodobenzo[b]furan derivatives were conveniently prepared from the corresponding 2-alkynylanilines and 2-alkynylphenols through Ph3P-catalyzed iodocyclization in the presence of N-iodosuccinimide (NIS). This protocol provides a rapid access to 3-iodoindoles and 3-iodobenzo[b]furans in good to excellent yields under mild conditions.
Ruthenium-Catalyzed Cycloisomerization of 2-Alkynylanilides: Synthesis of 3-Substituted Indoles by 1,2-Carbon Migration
作者:Takuma Watanabe、Yuichiro Mutoh、Shinichi Saito
DOI:10.1021/jacs.7b04564
日期:2017.6.14
We developed ruthenium-catalyzedcycloisomerization of alkynylanilides that gave 3-substituted indoles in high yields. The reaction proceeded via the disubstituted vinylidene ruthenium complex that was formed by the 1,2-carbon migration.
[Cp∗IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles
作者:Elumalai Kumaran、Weng Kee Leong
DOI:10.1016/j.tetlet.2014.08.053
日期:2014.10
[Cp*IrCl2](2) catalyses the cyclization of 2-alkynylanilines into indoles. A wide variety of substrates is tolerated. A reaction pathway involving intramolecular hydroamination is proposed. (C) 2014 Elsevier Ltd. All rights reserved.