Results
1 -
10 of
3485
(Click
here to explore results)
- 2-Pyridonates: a versatile ligand platform in 3d transition metal coordination chemistry and catalysis. Andrey Fedulin, Axel Jacobi von Wangelin
, Catal. Sci. Technol.
, 2024
, 14
, 26
- RhIII-promoted directed C–H N-heteroarylation of 2-pyridones. Rong Chi, Jia-Xue Wu, Da-Cheng Li, Jian-Min Dou, Huai-Wei Wang
, Org. Biomol. Chem.
, 2023
, 21
, 5288
- Lithiation of 4-methoxy-2-pyridones. Synthetic entry to tenellin and funiculosin, and related natural 3,5-disubstituted 4-oxy-2-pyridones. Judith Buck, J. Paul Madeley, Gerald Pattenden
, J. Chem. Soc., Perkin Trans. 1
, 1992
, 67
- Bioactive 2-pyridone-containing heterocycle syntheses using multicomponent reactions. Diana Hurtado-Rodríguez, Angélica Salinas-Torres, Hugo Rojas, Diana Becerra, Juan-Carlos Castillo
, RSC Adv.
, 2022
, 12
, 35158
- Metal-free regioselective direct thiolation of 2-pyridones. Kunita Phakdeeyothin, Sirilata Yotphan
, Org. Biomol. Chem.
, 2019
, 17
, 6432
- Synthesis and evaluation of new pirfenidone derivatives as anti-fibrosis agents. Chenxi Gu, Wei Li, Qing Ju, Han Yao, Lisheng Yang, Baijiao An, Wenhao Hu, Xingshu Li
, RSC Adv.
, 2022
, 12
, 14492
- Advances in the development of pyridinone derivatives as non-nucleoside reverse transcriptase inhibitors. Hugo Vite-Caritino, Oscar Méndez-Lucio, Héctor Reyes, Alberto Cabrera, Daniel Chávez, José L. Medina-Franco
, RSC Adv.
, 2016
, 6
, 2119
- Cyclic ureas as ortho directing substituents. Jon-Paul Meigh, Mercedes Álvarez, John A. Joule
, J. Chem. Soc., Perkin Trans. 1
, 2001
, 2012
- Selective synthesis of pyridyl pyridones and oxydipyridines by transition-metal-free hydroxylation and arylation of 2-fluoropyridine derivatives. Chunshu Liao, Jianrong Li, Xiaoqiong Chen, Jingjun Lu, Qiang Liu, Lu Chen, Yubing Huang, Yibiao Li
, Org. Biomol. Chem.
, 2020
, 18
, 1185
- Synthesis of trifluoromethylthiolated pyridinones through the copper-mediated trifluoromethylthiolation of iodopyridinones. Beibei Luo, Yunxiao Zhang, Yi You, Zhiqiang Weng
, Org. Biomol. Chem.
, 2016
, 14
, 8615