Three-component synthesis of new C3-substituted 5,6-dihydropyrrolo[2,1-a]isoquinolines
- Authors: Miftyakhova A.R.1, Sidakov M.B.1, Borisova T.N.1, Fakhrutdinov A.N.2, Titov A.A.1, Sorokina E.A.1, Varlamov A.V.1
- 
							Affiliations: 
							- Peoples’ Friendship University of Russia (RUDN University)
- N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
 
- Issue: Vol 59, No 9 (2023)
- Pages: 1131-1141
- Section: Articles
- URL: https://ruspoj.com/0514-7492/article/view/666184
- DOI: https://doi.org/10.31857/S0514749223090033
- EDN: https://elibrary.ru/XTXEVI
- ID: 666184
Cite item
Abstract
About the authors
A. R. Miftyakhova
Peoples’ Friendship University of Russia (RUDN University)
														Email: almira244@gmail.com
				                					                																			                												                														
M. B. Sidakov
Peoples’ Friendship University of Russia (RUDN University)
T. N. Borisova
Peoples’ Friendship University of Russia (RUDN University)
A. N. Fakhrutdinov
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
A. A. Titov
Peoples’ Friendship University of Russia (RUDN University)
E. A. Sorokina
Peoples’ Friendship University of Russia (RUDN University)
A. V. Varlamov
Peoples’ Friendship University of Russia (RUDN University)
References
- Xiang L., Xing D., Wang W., Wang R., Ding Y., Du L. Phytochemistry. 2005, 66, 2595-2601. doi: 10.1016/j.phytochem.2005.08.011
- Ballot C., Martoriati A., Jendoubi M., Buche S., Formstecher P., Mortier L., Kluza J., Marchetti P. Mar. Drugs. 2014, 12, 779-798. doi: 10.3390/md12020779
- Reyes-Gutiérrez P.E., Camacho J.R., Ramírez--Apan M.T., Osornio Y.M., Martínez R. Org. Biomol. Chem. 2010, 8, 4374-4382. doi: 10.1039/C004399K
- Fukuda T., Ishibashi F., Iwao M. Chem. Biol. 2020, 83, 1-112. doi: 10.1016/bs.alkal.2019.10.001
- Nevskaya A.A., Anikina L.V., Purgatorio R., Catto M., Nicolotti O., de Candia M., Pisani L., Borisova T.N., Miftyakhova A.R., Varlamov A.V., Nevskaya E.Y., Borisov R.S., Voskressensky L.G., Altomare C.D. Molecules. 2021, 26, 359. doi: 10.3390/molecules26020359
- Tangdenpaisal K., Worayuthakarn R., Karnkla S., Ploypradith P., Intachote P., Sengsai S., Saimanee B., Ruchirawat S., Chittchang M. Chem. Asian J. 2015, 10, 925-937. doi: 10.1002/asia.201403361
- Reddy M.V.R., Rao M.R., Rhodes D., Hansen M.S.T., Rubins K., Bushman F.D., Venkateswarlu Y., Faulkner D.J. J. Med. Chem. 1999, 42, 1901-1907. doi: 10.1021/jm9806650
- Su B., Cai C., Deng M., Liang D., Wang L., Wang Q. Bioorg. Med. Chem. Lett. 2014, 24, 2881-2884. doi: 10.1016/j.bmcl.2014.04.101
- Fukuda T., Ishibashi F., Iwao M. Heterocycles. 2011, 83, 491. doi: 10.3987/REV-10-686
- Maryanoff B.E., Vaught J.L., Shank R.P., McComsey D.F., Costanzo M.J., Nortey S.O. J. Med. Chem. 1990, 33, 2793-2797. doi: 10.1021/jm00172a018
- Shang Z.H., Zhang X.J., Li Y.M., Wu R.X., Zhang H.R., Qin L.Y., Ni X., Yan Y., Wu A.X., Zhu Y.P. J. Org. Chem. 2021, 86, 15733-15742. doi: 10.1021/acs.joc.1c01682
- Yue Y., Sun Y., Zhao S., Yan X., Li R., Shi Y., Zhuo K., Liu J. Chem. Asian J. 2016, 11, 3339-3344. doi: 10.1002/asia.201601233
- Alizadeh A., Rostampoor A. ChemistrySelect. 2021, 6, 12960-12964. doi: 10.1002/slct.202103675
- Tao L., Xu Z., Han J., Deng H., Shao M., Chen J., Zhang H., Cao W. Synthesis. 2016, 48, 4228-4236. doi: 10.1055/s-0035-1562624
- Wu F.S., Zhao H.Y., Xu Y.L., Hu K., Pan Y.M., Ma X.L., J. Org. Chem. 2017, 82, 4289-4296. doi: 10.1021/acs.joc.7b00280
- Ghosh A., Kolle S., Barak D.S., Kant R., Batra S. ACS Omega. 2019, 24, 20854-20867. doi: 10.1021/acsomega.9b03546
- Dumitrascu F., Georgescu E., Georgescu F., Popa M.M., Dumitrescu D. Molecules. 2013, 18, 2635-2645. doi: 10.3390/molecules18032635
- Zhou W., Liu H., Guo Y., Gu Y., Han J., Chen J., Deng H., Shao M., Zhang H., Cao W. J. Fluor. Chem. 2019, 222, 51-58. doi: 10.1016/j.jfluchem.2019.04.015
- Tang E., Mao D., Sun Q., Liao M., Li Y., Liu S. Heterocycles. 2019, 98, 1563-1573. doi: 10.3987/COM-19-14162
- Wang W., Sun J., Hu H., Liu Y. Org. Biomol. Chem. 2018, 16, 1651-1658. doi: 10.1039/C7OB03048G
- Miftyakhova A.R., Borisova T.N., Titov A.A., Sidakov M.B., Novikov R.A., Efimov I.V., Varlamov A.V., Voskressensky L.G. Chem. Biodivers. 2022, 19, e202100584. doi: 10.1002/cbdv.202100584
- Miftyakhova A.R., Sidakov M.B., Borisova T.N., Ilyushenkova V.V., Fakhrutdinov A.N., Sorokina E.A., Varlamov A.V., Voskressensky L.G. Tetrahedron Lett. 2022, 103, 153991. doi: 10.1016/j.tetlet.2022.153991
- Voskressensky L.G., Borisova T.N., Matveeva M.D., Khrustalev V.N., Titov A.A., Aksenov A.V., Dyachenko S.V., Varlamov A.V. Tetrahedron Lett. 2017, 58, 877-879. doi: 10.1016/j.tetlet.2017.01.061
- Matveeva M., Golovanov A., Borisova T., Titov A., Varlamov A., Shaabani A., Obydennik A., Voskressensky L. Mol. Catal. 2018, 461, 67-72. doi: 10.1016/j.mcat.2018.09.020
Supplementary files
 
				
			 
					 
						 
						 
						 
						 
									

 
  
  
  Email this article
			Email this article 
 Open Access
		                                Open Access Access granted
						Access granted Subscription or Fee Access
		                                							Subscription or Fee Access
		                                					