[1]
Arora, P.; Arora, V.; Lamba, H.S.; Wadhwa, D. Importance of heterocyclic chemistry: A review. IJPSR, 2012, 3, 2947-2954.
[3]
Kaur, R.; Rani, V.; Abbot, V.; Kapoor, Y.; Konar, D.; Kumar, K. Recent synthetic and medicinal perspectives of pyrroles: An overview. J. Pharm. Chem. Chem. Sci., 2017, 1, 17-32.
[14]
Sundberg, R.J. In Comprehensive Heterocyclic Chemistry; II; Katritzky,
A. R.; Rees, C. W.; Scriven, E. F. V.; Eds.. Pergamon Press:
Oxford, 1996. 2, p. 119.
[17]
Mal, D.; Shome, B.; Dinda, B.K. Pyrrole and Its Derivatives;, Heterocycles
in natural product synthesis. 2011, 187-220.
[28]
For a symposium in print on MCRs, see: Tetrahedron Symposia-in-
Print, ed. I. Marek 2005, vol. 67 p. 11299. Tejedor, D.; Garcia-Tellado, F. Chemo-Differentiating ABB' multicomponent reactions. privileged building blocks.. Chem. Soc. Rev , 2007, 36, 484-491.
[49]
Mashkovskii, M.D. Drugs [in Russian]; Kharkov, 1997, 2, p. 331, , 375-422.
[53]
Mohammat, M.F.; Najim, N.; Mansor, N.S.; Sarman, S.; Shaameri, Z.; Zain, M.M.; Hamzan, A.S. Synthesis and bioactivity of some 2-oxo-5-aryl-3-hydrazone and 2-oxo-5-aryl-4-hydrazone pyrrolidine derivatives. ARKIVOC, 2011, 429-438.
[55]
Manta, S.; Tzioumaki, N.; Kollatos, N.; Andrea, P.; Panagiotopoulou, P.; Papanastasiou, I.; Mitsos, C.; Tsotinis, A.; Schols, D.; Komiotis, D. A novel and easy two-step, microwave-assisted method for the synthesis of halophenyl pyrrolo quinoxalines via their pyrrolo precursors evaluation of their bioactivity. Curr. Microw. Chem., 2018, 5, 1873-1876.
[62]
Mashkovskii, M.D. ekarstvennye sredstva (Drugs), Moscow: RIA ; Novaya Volna. , 2012.
[63]
Gein, V.L.; Kasimova, N.N.; Aliev, Z.G.; Vakhrin, M.I. Three-component reaction of methyl 2,4-dioxo-4-phenylbutanoate and methyl 2,4-dioxopentanoate with aromatic aldehydes and propane-1,2-diamine and chemical properties of the products. Russ. J. Gen. Chem., 2010, 46, 875-883.
[64]
Khan, M.S.Y.; Gupta, M. Synthesis, antiinflammatory and analgesic activity of new hexahydropyrimidine derivatives. Pharmazie, 2002, 57, 377-383.