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- Access to 5H-benzo[a]carbazol-6-ols and benzo[6,7]cyclohepta[1,2-b]indol-6-ols via rhodium-catalyzed C–H activation/carbenoid insertion/aldol-type cyclization. Yumeng Yuan, Xiemin Guo, Xiaofeng Zhang, Buhong Li, Qiufeng Huang
, Org. Chem. Front.
, 2020
, 7
, 3146
- Selective synthesis of indazoles and indoles via triazene–alkyne cyclization switched by different metals. Yan Fang, Chengming Wang, Shengqin Su, Haizhu Yu, Yong Huang
, Org. Biomol. Chem.
, 2014
, 12
, 1061
- Unravelling the synthetic and therapeutic aspects of five, six and fused heterocycles using Vilsmeier–Haack reagent. Mamta Chahal, Sudeep Dhillon, Priyanka Rani, Ginna Kumari, Deepak Kumar Aneja, Mayank Kinger
, RSC Adv.
, 2023
, 13
, 26604
- Synthesis of 2-arylindole derivatives and evaluation as nitric oxide synthase and NFκB inhibitors. Xufen Yu, Eun-Jung Park, Tamara P. Kondratyuk, John M. Pezzuto, Dianqing Sun
, Org. Biomol. Chem.
, 2012
, 10
, 8835
- Vilsmeier–Haack reaction of 7-acetyl-2-arylindoles: a convenient method for the synthesis of 6-oxo-6H-pyrrolo[3,2,1-ij]quinoline-1,5-dicarbaldehydes. Malose J. Mphahlele, Mmakwena M. Mmonwa
, Org. Biomol. Chem.
, 2019
, 17
, 2204
- An expedient route to tricyanovinylindoles and indolylmaleimides from o-alkynylanilines utilising DMSO as a one-carbon synthon. Nikita Chakraborty, Anjali Dahiya, Amitava Rakshit, Anju Modi, Bhisma K. Patel
, Org. Biomol. Chem.
, 2021
, 19
, 6847
- Pd-catalyzed dehydrogenative C–H activation of iminyl hydrogen with the indole C3–H and C2–H bond: an elegant synthesis of indeno[1,2-b]indoles and indolo[1,2-a]indoles. Somjit Hazra, Biplab Mondal, Rajendra Narayan De, Brindaban Roy
, RSC Adv.
, 2015
, 5
, 22480