Diastereoselective green synthesis of pyrrolo[1,2-a]quinolines via [3+2] cycloaddition reaction: insights from molecular electron density theory
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry
Link
https://link.springer.com/content/pdf/10.1007/s00214-023-03068-8.pdf
Reference86 articles.
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2. Carbone A, Pennati M, Parrino B, Lopergolo A, Barraja P, Montalbano A, Spanò V, Sbarra S, Doldi V, De Cesare M (2013) Novel 1 H-pyrrolo [2, 3-b] pyridine derivative nortopsentin analogues: synthesis and antitumor activity in peritoneal mesothelioma experimental models. J Med Chem 56:7060–7072. https://doi.org/10.1021/jm400842x
3. Al-Matarneh MC, Amărandi R-M, Mangalagiu II, Danac R (2021) Synthesis and biological screening of new cyano-substituted pyrrole fused (iso) quinoline derivatives. Molecules 26:2066. https://doi.org/10.3390/2Fmolecules26072066
4. Hosseyni Largani T, Imanzadeh G, Zahri S, Noroozi Pesyan N, Şahin E (2017) A facile synthesis and antibacterial activity of novel pyrrolo [3, 4-b] quinolin-2 (3H)-yl) benzamides. Green Chem Lett Rev 10:387–392. https://doi.org/10.1080/17518253.2017.1380233
5. Mondal A, Gandhi A, Fimognari C, Atanasov AG, Bishayee A (2019) Alkaloids for cancer prevention and therapy: current progress and future perspectives. Eur J Pharmacol 858:172472. https://doi.org/10.1016/j.ejphar.2019.172472
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