Three-component synthesis of trisubstituted pyridin-2(1H)-ones
- Autores: Talybov G.M.1
-
Afiliações:
- Azerbaijan Technical University
- Edição: Volume 60, Nº 5 (2024)
- Páginas: 683-687
- Seção: Articles
- URL: https://rjonco.com/0514-7492/article/view/685348
- DOI: https://doi.org/10.31857/S0514749224050127
- EDN: https://elibrary.ru/RCQTLW
- ID: 685348
Citar
Resumo
Condensation of aryl cyanides with chloromethylpropargyl(allyl) ethers and ethylphenylpropiolate in the presence of pyridine leads to trisubstituted pyridin-2(1H)-ones.
Palavras-chave
Texto integral

Sobre autores
G. Talybov
Azerbaijan Technical University
Autor responsável pela correspondência
Email: gtalibov61@gmail.com
ORCID ID: 0000-0001-6251-2974
Azerbaijão, prosp. G. Javida, 25, Baku, AZ 1073
Bibliografia
- Dean A. Wacker,Ying Wang, Matthias Broekema, Karen Rossi, Steven O’Connor,Zhenqiu Hong, Ginger Wu, Sarah E. Malmstrom, Chen-Pin Hung, Linda LaMarre. Anjaneya Chimalakonda, Lisa Zhang, Li Xin, Hong Cai, Cuixia Chu, Stephanie Boehm, Jacob Zalaznick, Randolph Ponticiello, Larisa Sereda, Song-Ping Han, Rachel Zebo, Bradley Zinker, Chiuwa Emily Luk, Richard Wong, Gerry Everlof, Yi-Xin Li, Chunyu K. Wu, Michelle Lee, Steven Griffen, Keith J. Miller, John Krupinski, Jeffrey A. Robl. J. Med. Chem. 2014, 57, 7499–7508. https://doi.org/10.1021/jm501175v
- V.S. Prasadarao Lingam, Dnyaneshwar H. Dahale, Vijay E. Rathi, Yogesh B. Shingote, Rajni R. Thakur, Ajit S. Mindhe, Srinivas Kummari, Neelima Khairatkar-Joshi, Malini Bajpai, Daisy M. Shah, Ratika S. Sapalya, Srinivas Gullapalli, Praveen K. Gupta, Girish S. Gudi, Satyawan B. Jadhav, Rambabu Pattem, Abraham Thomas. J. of Med. Chem. 2015, 58, 8292–8308. https://doi.org/10.1021/acs.jmedchem.5b01240
- James F. Blake, Michael Burkard, Jocelyn Chan, Huifen Chen, Kang-Jye Chou, Dolores Diaz, Danette A. Dudley, John J. Gaudino, Stephen E. Gould, Jonas Grina, Thomas Hunsaker, Lichuan Liu, Matthew Martinson, David Moreno, Lars Mueller, Christine Orr, Patricia Pacheco, Ann Qin, Kevin Rasor, Li Ren, Kirk Robarge, Sheerin Shahidi-Latham, Jeffrey Stults, Francis Sullivan, Weiru Wang, Jianping Yin, Aihe Zhou, Marcia Belvin, Mark Merchant, John Moffat,Jacob B. Schwarz. J. Med. Chem. 2016, 59, 5650–5660. https://doi.org/10.1021/acs.jmedchem.6b00389
- Alvarez S., Medina S., Domínguez G., Perez-Castells J. J. Org. Chem. 2013, 78, 9995. https://doi.org/10.1021/jo401538p
- Kiet Le Van, Christine Cauvin, Ste phane de Walque,| Benoıˆt Georges Sandro Boland, Vale rie Martinelli, Dominique Demonte, Franc ois Durant, La ´szlo ´ Hevesi,and Carine Van Lint. J. Med. Chem. 2009, 52, 3636. https://doi.org/10.1021/jm801438e
- Tushar Apsunde, Ryan P. Wurz. J. Org. Chem. 2014, 79, 3260. https://doi.org/ 10.1021/jo400541s
- Hartmut Schirok, Cristina Alonso-Alija, Jordi Benet-Buchholz, Andreas H. Go ¨ller, Rolf Grosser, Martin Michels, and Holger Paulsen. J. Org. Chem. 2005, 70, 9463.
- Wei Pan, Dewen Dong, Kewei Wang, Jie Zhang, Rigenhada Wu, Dexuan Xiang,Qun Liu. Organic Letters 2007, 9, 2421–2423. https://doi.org/10.1021/ol070905i
- Sandip Chikhalikar, Vijay Bhawe, Bhausaheb Ghotekar, Madhukar Jachak,Maruti Ghagare. J. Org. Chem. 2011, 76, 10, 3829–3836. doi: 10.1021/jo200197g.
- Cécile Croix, Gildas Prié, Charlotte Chaulet, Marie-Claude Viaud-Massuard. J. Org. Chem. 2015, 80, 3264–3269. https://doi.org/ 10.1021/jo502784.
- Dexuan Xiang, Kewei Wang, Yongjiu Liang, Guangyuan Zhou, Dewen Dong. Org. Let. 2008, 10, 2, 345–348. https://doi.org/10.1021/ol702846t
- Талыбов Г.М. ЖОрХ, 2017, 53, 124–125. (Talybov G.M. New synthesis of 1,2-diol monopropargyl ethers. Russ. J. Org. Chem. 2017, 53, 123–124. https://doi.org/10.1134/S1070428017010225
- Blaise, E.E. C. R. Hebd. Seances Acad. Sci. 1901, 132, 478–480.
Arquivos suplementares
