References
- J. H. Lee and J. Lee, FEMS Microbiol. Rev., 34, 426 (2010).
- N. K. Kaushik, N. Kaushik, P. Attri, N. Kumar, C. H. Kim, A. K. Verma, and E. H. Choi, Molecules, 18, 6620 (2013).
- M. Colella, L. Degennaro, and R. Luisi, Molecules, 25, 3242 (2020).
- V. Sravanthi and S. L. Manju, Eur. J. Pharma. Sci., 91, 1 (2016).
- S. M. Basavarajaiah and B. H. M. Mruthyunjayaswamy, Indian J. Chem., 57B, 390–399 (2018).
- A. Kumari and R. K. Singh, Bioorg. Chem., 89, 103021 (2019).
- D. F. Taber and P. K. Tirunahari, Tetrahedron, 67, 7195 (2011).
- S. M. Basavarajaiah, G. Y. Nagesh, N. B. Jeelan, and B. Jaishree, Tet. Lett., 85, 153458 (2021).
- R. Mancuso and R. Dalpozzo, Catalysts, 8, 458 (2018).
- R. Vicente, Org. Biomol. Chem., 9, 6469 (2011).
- S. M. Basavarajaiahand and B. S. Sasidhar, J. Mol. Struct., 1261, 132808 (2022).
- S. Kumar and Ritika, Future J. Pharm Sci., 6, 121 (2020).
- V. T. Punniyakoti, K. M. Rahul, G. Vishali, and M. Vikramdeep, Eur. J. Med. Chem., 180, 562 (2019).
- B. S. Matada, R. Pattanashettar, and N. G. Yernale, Bioorg. Med. Chem., 32, 115973 (2021).
- B. S. Matada and N. G. Yernale, Synth. Commun., 51, 1133(2021).
- B. S. Matada and N. G. Yernale, J. Indian Chem. Soc., 98, 100174 (2021).
- a) B. S. Matada, N. G. Yernale, and M. Javeed, Polycycl. Aromat. Compd, DOI: 10.1080/10406638.2021.2019062. b). B. S. Mathada (2022) Polycycl. Aromatic Compd., DOI: 10.1080/10406638.2022.2089177. c) N. J. Basha, S. M. Basavarajaiah, Polycycl. Aromat. Compd., DOI: 10.1080/10406638.2022.2080728.
- S. M. Basavarajaiah, G. Y. Nagesh, and B. Jeelan N, vol. 1, Phys. Sci. Rev., DOI: 10.1515/psr-2021-0040
- a) N. J. Basha, S. M. Basavarajaiah, and K. Shyamsunder, Mol. Divers., DOI: 10.1007/s11030-022-10387-8. b) S. M. Basavarajaiah, G. Y. Nagesh, M. Javeed, R. Bhat, S. Nethravathi, J. Basha, K. Ramakrishna Reddy, C. Nisarga, and P. Srinivas, Mol Divers., DOI: 10.1007/s11030-022-10448-y.
- N. J Basha, S. M. Basavarajaiah, B. Swathi, and K. Prasanna, Nat. Prod. Res., DOI: 10.1080/14786419.2021.1955361.
- R. Nalini, S. M. Basavarajaiah, G. Y. Nagesh, and R. K. Ramakrishna, Asian J. Chem., 34, 389 (2022).
- G. Y. Nagesh, M. Javeed, J. N. Basha, K. Prashantha, R. Nithin, P. R. Thanushree, S. Vivekananda, S. S. Gowda, H. B. Punarva, and S. M. Basavarajaiah, J. Mol. Struct., 1262, 132977 (2022).
- K. N. Sheshandrakumar, J. Srividya, B. J. Narayanaswamy, K. Umesha, and S. M. Basavarajaiah, Indian J. Heterocycl. Chem., 27, 281(2017).
- B. H. M. Mruthyunjayaswamy, B. K. Shanthaveerappa, and S. M. Basavarjaiah, J. Indian Chem. Soc., 87, 1109 (2010).
- Z. Wang, “Comprehensive Organic Name Reactions and Reagents”, vol. 1-3, pp. 10–102, New York, Wiley Online Library, 2010.
- E. Fischer and F. Jourdan, Ber. Dtsch. Chem. Ges., 16, 2241 (1883).
- E. Fischer and O. Hess, Ber. Dtsch. Chem. Ges., 17, 559 (1884).
- P. G. Gassman, T. J. van Bergen, D. P. Gilbert, and W. Cue. Jr.Berkeley, J. Am. Chem. Soc., 96, 5495 (1974).
- J. J. Li,“Bischler-Mohlau Indole Synthesis,” in “Name Reactions,” Berlin, Springer, 2009.
- T. Sugasawa, M. Adachi, K. Sasakura, and A. Kitagawa, J. Org. Chem., 44, 578 (1979).
- “Buchwald Indoline Synthesis,” in “Comprehensive Organic Name Reactions and Reagents,” New York, Wiley Online Library, DOI: 10.1002/9780470638859.conrr125.
- G. Bartoli, R. Leardini, A. Medici, and G.J. Rosini, Chem. Soc. Perkin Trans., 1, 692 (1978).
- W. Madelung, Ber. Dtsch. Chem. Ges., 45, 1281 (1912).
- C. D. Nenitzescu, Bull. Soc. Chim. Romania, 11, 37 (1929).
- T. Fukuyama, X. Chen, and G. Peng, J. Am. Chem. Soc., 116, 3127 (1994).
- L. Fra, A. Millán, J. A. Souto, and K. Muñiz, Angew. Chem. Int. Ed. Engl., 53, 7349 (2014).
- Y. H. Jang and S. W. Youn, Org. Lett., 16, 3720 (2014).
- Y. -L. Li, J. Li, A.-L. Ma, Y.-N. Huang, and J. Deng, J. Org. Chem., 80, 3841 (2015).
- S. Ortgies and A. Breder, Org. Lett., 17, 2748 (2015).
- M. Wu and R. Yan, Synlett., 28, 729 (2017).
- A. Andries-Ulmer, C. Brunner, J. Rehbein, and T. Gulder, J. Am. Chem. Soc., 140, 13034 (2018).
- H.D. Xia, Y.D. Zhang, Y.-H. Wang, and C. Zhang, Org. Lett.,20, 4052 (2018).
- J. Ni, Y. Jiang, Z. An, and R. Yan, Org. Lett., 20, 1534 (2018).
- K. Hu, Y. Zhang, Z. Zhou, Y. Yang, Z. Zha, and Z. Wang, Org. Lett., 22, 5773 (2020).
- A. Kutznetsov, A. Makarov, A. E. Rubtsov, A. V. Butin, and V. Gevorgyan, J. Org. Chem., 78, 12144 (2013).
- E. Boess, S. Karanestora, A.-E. Bosnidou, B. Schweitzer-Chaput, M. Hasenbeck, and M. Klussmann, Synlett., 26, 1973 (2015).
- J. Panther, J. Rechmann, and T. Müller, Chem. Heterocycl. Comp., 52, 897 (2016).
- Y. Qiu, K. T. Puni, C. C. Duplan, A. C. Lindsay, and J. Sperry, Tetrahedron Lett., 72, 153068 (2021).
- S. Gore, S. Baskaran, and B. König, Org. Lett., 14, 4568 (2012).
- G. Satta, E. Usala, A. Solinas, M. Römer, M. Livesi, G. M. Pira, A. Beccu, S. Carboni, S. Gaspa, L. D. Luca, L Pisano, U. Azzena, and M. Carraro, Eur. J. Org. Chem., 2021, 5835 (2021).
- J. Yao, Y. Xie, L. Zhang, Y. Li, and H. Zhou, Beilstein J. Org. Chem., 13, 1866 (2017).
- D. I. Bugaenko, A. A. Dubrovina, M. A. Yurovskaya, and A.V. Karchava, Org. Lett., 20, 7358 (2018).
- D. Tejedor, R. Diana-Rivero, and F. A. García-Tellado, Molecules, 25, 5595 (2020).
- J. Mao, Z. Wang, X. Xu, G. Liu, R. Jiang, H. Guan, Z. Zheng, and P. J. Walsh, Angew. Chem.Int. Ed., 58, 11033 (2019).
- A. R. Raju, R. V. Reddy, V. M. Rao, V. V. Naresh, and A. V. Rao, Tetrahedron Lett., 57, 2838 (2016).
- G. A. Chesnokov, A. A. Ageshina, M. A. Topchiy, M. S. Nechaev, and A. F. Asachenko, Eur. J. Org. Chem., 30, 4844 (2019).
- Y.-W. Li, H.-X. Zheng, B. Yang, X.-H. Shan, J. -P. Qu, and Y.-B. Kang, Org. Lett., 22, 4553 (2020).
- H. Chung, J. Kim, G. A. G.-Montiel, P. H.-Y. Cheong, and H. G. Lee, Org. Lett., 23, 1096 (2021).
- P. Yang, W. Xu, R. Wang, M. Zhang, C. Xie, X. Zeng, and M. Wang, Org. Lett., 21, 3658 (2019).
- Y. Zhao, D. Li, L. Zhao, and J. Zhang, Synthesis, 6, 873 (2011).
- R. Reddy, K. Adlak, and P. Ghorai, J. Org. Chem., 82, 8426 (2017).
- P. Jiang, S. Chen, H. Huang, K. Hu, Y. Xia, and G.-J. Deng, Green Synth. Catal., 2, 78 (2021).
- B. Zhang, X. Li, X. Li, Z. Yu, B. Zhao, X. Wang, Y. Du, and K. Zhao, J. Org. Chem., 86, 17274 (2021).
- N. Yadav, M. D. Ansari, V. B. Yadav, A. Verma, S. K. Tiwari, S, Ansari, and I. R. Siddiqui, Mol. Divers., 25, 1103 (2021)
- S. Das, A. Azim, S. K. Hota, S. P. Panda, S. Murarka, and S. D. Sarkar, Chem. Commun., 57, 13130 (2021).
- W. Sun, W. A. T. Raimbach, L. D. Elliott, K. I. Booker-Milburn, and D. C. Harrowven, Chem. Commun., 58, 383 (2022).
- T. -L. Wang, B. -S. Zhang, J. -J. Liu, X. -J. Liu, X. -C. Wang, and Z. -J. Quan, Org. Chem., Front., 4, 1004 (2022).
- Q. Huang, M. Zhao, Y. Yang, Y.-N. Niu, and X.-F. Xia, Org. Chem. Front., 8, 5988 (2021).
- M. Ebrahimi, D. Arefi, and R. S. Khoshnood, Moroc. J. Chem., 8, 218 (2020).
- T.-H. Ding, Z.-F. Xiao, J.-P. Qu, and Y.-B. Kang, J. Org. Chem., 83, 2467 (2018).
- A. C. Lindsay, P. A. Kilmartin, and J. Sperry, Org. Biomol. Chem., 19, 7903 (2021).