Recent advances in the synthesis and biological activities of 3-aminoalkyl/3-amidoalkyl-4-hydroxycoumarin derivatives

References

• Irena, K. Curr. Med. Chem. Anti Cancer Agents 2005, 5, 29–46.
   PubMedGoogle Scholar
• Milenkovic, D. A.; Dimic, D. S.; Avdovic, E. H.; Markovic, Z. S. RSC Adv. 2020, 10, 35099–35108. DOI: 10.1039/D0RA07062A.
   PubMed Web of Science ®Google Scholar
• Mayekar, S. A.; Chaskar, A. C.; Mulwad, V. V. Synth. Commun. 2009, 40, 46–51. DOI: 10.1080/00397910902916080.
   Web of Science ®Google Scholar
• Razavi, S. M. Int. J. Biol. Chem. 2011, 51, 86–90.
   Google Scholar
• Abdel-Aziem, A.; Baaiu, B. S.; Elbazzar, A. W.; Elabbar, F. Synth. Commun. 2020, 50, 2522–2530. DOI: 10.1080/00397911.2020.1782431.
   Web of Science ®Google Scholar
• Kumar, S.; Aggarwal, R.; Sharma, C. Synth. Commun. 2015, 45, 2022–2029. DOI: 10.1080/00397911.2015.1062986.
   Web of Science ®Google Scholar
• Kasabe, A.; Mohite, V.; Ghodake, J.; Vidhate, J. Eur. J. Chem. 2010, 7, 377–382.
   Google Scholar
• Sanad, S. M. H.; Mekky, A. E. M. Synth. Commun. 2020, 50, 1468–1485. DOI: 10.1080/00397911.2020.1743318.
   Web of Science ®Google Scholar
• Zhang, W.; Li, Z.; Zhou, M.; Wu, F.; Hou, X.; Luo, H.; Liu, H.; Han, X.; Yan, G.; Ding, Z.; Li, R. Bioorg. Med. Chem. Lett. 2014, 24, 799–807. DOI: 10.1016/j.bmcl.2013.12.095.
   PubMed Web of Science ®Google Scholar
• Khoobi, M.; Alipour, M.; Sakhteman, A.; Nadri, H.; Moradi, A.; Ghandi, M.; Emami, S.; Foroumadi, A.; Shafiee, A. Eur. J. Med. Chem. 2013, 68, 260–269. DOI: 10.1016/j.ejmech.2013.07.038.
   PubMed Web of Science ®Google Scholar
• Završnik, D.; Muratović, S.; Makuc, D.; Plavec, J.; Cetina, M.; Nagl, A.; Clercq, E. D.; Balzarini, J.; Mintas, M. Molecules 2011, 16, 6023–6040. DOI: 10.3390/molecules16076023.
   PubMed Web of Science ®Google Scholar
• Arya, A. K.; Rana, K.; Kumar, M. LDDD 2013, 11, 594–600. DOI: 10.2174/1570180811666131210000903.
   Google Scholar
• Tasdemir, D.; Kaiser, M.; Brun, R.; Yardley, V.; Schmidt, T. J.; Tosun, F.; Rüedi, P. Antimicrob Agents Chemother. 2006, 50, 1352–1364. DOI: 10.1128/AAC.50.4.1352-1364.2006.
   PubMed Web of Science ®Google Scholar
• Tiwari, N.; Kumari, A.; Uttam, G.; Singh, V.; Singh, K.; Katiyar, D. ChemistrySelect 2022, 7, e202201299. DOI: 10.1002/slct.202201299.
   Web of Science ®Google Scholar
• Wang, M.; Chen, F.; Guan, J.; Zhao, J.; Zhang, J.; Zhao, R. Appl. Biochem. Biotechnol. 2009, 159, 768–777. DOI: 10.1007/s12010-009-8619-7.
   PubMed Web of Science ®Google Scholar
• Oliva, A.; Meepagala, K. M.; Wedge, D. E.; Harries, D.; Hale, A. L.; Aliotta, G.; Duke, S. O. J. Agric. Food Chem. 2003, 51, 890–896. DOI: 10.1021/jf0259361.
   PubMed Web of Science ®Google Scholar
• Abdou, M. M.; El-Saeed, R. A.; Bondock, S. Arab. J. Chem. 2019, 12, 88–121. DOI: 10.1016/j.arabjc.2015.06.012.
   Web of Science ®Google Scholar
• Robertson, D. N.; Link, K. P. J. Am. Chem. Soc. 1953, 75, 1883–1885. DOI: 10.1021/ja01104a031.
   Web of Science ®Google Scholar
• Savel’ev, V. L.; Artamonova, O. S.; Troitskaya, V. S.; Shavyrina, V. V.; Afanas’eva, T. G.; Zagorevskii, V. A. Chem. Heterocycl. Compd. 1982, 18, 676–679. DOI: 10.1007/BF00568940.
   Google Scholar
• Mukhopadhyay, C.; Rana, S.; Butcher, R. J. Synth. Commun. 2012, 42, 3077–3088. DOI: 10.1080/00397911.2011.575524.
   Web of Science ®Google Scholar
• Borah, P.; Naidu, P. S.; Bhuyan, P. J. Synth. Commun. 2015, 45, 1533–1540. DOI: 10.1080/00397911.2015.1027405.
   Web of Science ®Google Scholar
• Milevskii, B. G.; Chibisova, T. A.; Solov´eva, N. P.; Sukhorukov, A. Y.; Traven, V. F. Russ Chem. Bull. 2015, 64, 423–428. DOI: 10.1007/s11172-015-0879-5.
   Web of Science ®Google Scholar
• Montagut-Romans, A.; Boulven, M.; Lemaire, M.; Popowycz, F. RSC Adv. 2016, 6, 4540–4544. DOI: 10.1039/C5RA22440C.
   Web of Science ®Google Scholar
• Kiani, A.; Jalili-Baleh, L.; Abdolahi, Z.; Nadri, H.; Foroumadi, A.; Ebrahimi, S. E. S.; Khoobi, M. J. Sci. I. R. I. 2019, 30, 5–12.
   Google Scholar
• Vukovic, N.; Sukdolak, S.; Solujic, S.; Niciforovic, N. Arch. Pharm. Res. 2010, 33, 5–15. DOI: 10.1007/s12272-010-2220-z.
   PubMed Web of Science ®Google Scholar
• Kumar, A.; Gupta, M. K.; Kumar, M. Tetrahedron Lett. 2011, 52, 4521–4525. DOI: 10.1016/j.tetlet.2011.06.040.
   Web of Science ®Google Scholar
• Rao, P.; Konda, S.; Iqbal, J.; Oruganti, S. Tetrahedron Lett. 2012, 53, 5314–5317. DOI: 10.1016/j.tetlet.2012.07.098.
   Web of Science ®Google Scholar
• Alagiri, K.; Devadig, P.; Prabhu, K. R. Chemistry 2012, 18, 5160–5164. DOI: 10.1002/chem.201200100.
   PubMed Web of Science ®Google Scholar
• Onkara, P.; Sunil Kumar, A.; Kanakaraju, S.; Prasanna, B.; Pydisetty, Y.; Chandramouli, G. V. P. Int. J. Pharm. Bio. Sci. 2013, 4, 263–270.
   Google Scholar
• Viradiya, D. J.; Kotadiya, V. C.; Khunt, M. D.; Baria, B. H.; Bhoya, U. C. ILCPA 2014, 30, 177–184. DOI: 10.56431/p-v4vn9w.
   Google Scholar
• Zahiri, S.; Mokhtary, M. J. Taibah Univ. Sci. 2015, 9, 89–94. DOI: 10.1016/j.jtusci.2014.09.006.
   Web of Science ®Google Scholar
• Ghandi, M.; Babazadeh, E. J. Iran Chem. Soc. 2015, 12, 379–387. DOI: 10.1007/s13738-014-0494-7.
   Web of Science ®Google Scholar
• Lin, H.; Tan, Y.; Wu, J.-M.; Yang, X.-D.; Chen, J.-H.; Sun, X.-W. Tetrahedron Lett. 2015, 56, 913–917. DOI: 10.1016/j.tetlet.2014.12.138.
   Web of Science ®Google Scholar
• Ghashang, M.; Shafiee, M. R. M.; Delzendeh, S.; Fazlinia, A.; Esfandiari, H.; Biregan, M. N.; Heydari, N. Bulg. Chem. Commun 2016, 48, 694–697.
   Web of Science ®Google Scholar
• Zaheer, Z.; Kalam Khan, F. A.; Sangshetti, J. N.; Patil, R. H. Chin. Chem. Lett. 2016, 27, 287–294. DOI: 10.1016/j.cclet.2015.10.028.
   Web of Science ®Google Scholar
• Baghery, S.; Zolfigol, M. A.; Schirhagl, R.; Hasani, M. Catal Lett. 2017, 147, 2083–2099. DOI: 10.1007/s10562-017-2096-3.
   Web of Science ®Google Scholar
• Olyaei, A.; Dortaj, E.; Khoeiniha, R.; Rajabi, F. J. J. Heterocyclic Chem. 2018, 55, 2971–2976. DOI: 10.1002/jhet.3379.
   Web of Science ®Google Scholar
• Olyaei, A.; Ghahremany, Z.; Sadeghpour, M. LOC 2022, 19, 208–213. DOI: 10.2174/1570178618666210615101248.
   Web of Science ®Google Scholar
• Ghosh, P. P.; Das, A. R. Tetrahedron Lett 2012, 53, 3140–3143. DOI: 10.1016/j.tetlet.2012.04.033.
   Web of Science ®Google Scholar
• Anaraki-Ardakani, H.; Mirza, B.; Mokhtarian, N. J. Appl. Chem. Res. 2015, 9, 103–110.
   Google Scholar
• Sangshetti, J. N.; Khan, F. A. K.; Kute, C. S.; Zaheer, Z.; Ahmed, R. Z. Russ. J. Org. Chem. 2015, 51, 69–73. DOI: 10.1134/S107042801501011X.
   Web of Science ®Google Scholar
• Dehghan, A.; Shams, N. Indian J. Fundam. Appl. Life Sci. 2015, 5, 5288–5293.
   Google Scholar
• Pournajaf, R.; Hassanzadeh-Tabrizi, S. A. J. Sol-Gel Sci. Technol. 2015, 75, 360–365. DOI: 10.1007/s10971-015-3708-2.
   Web of Science ®Google Scholar
• Ghafuri, H.; Ghorbani, B.; Rashidizadeh, A.; Talebi, M.; Roshani, M. Appl. Organometal Chem. 2018, 32, e4147. DOI: 10.1002/aoc.4147.
   Web of Science ®Google Scholar
• Geetha, S.; Thangamani, A.; Valliappan, R.; Vedanayaki, S.; Ganapathi, A. Chem. Data Collect. 2020, 30, 100589. DOI: 10.1016/j.cdc.2020.100589.
   Google Scholar
• Rabiei, K.; Niyazi, S. Polycycl. Aromat. Compd. 2022. DOI: 10.1080/10406638.2022.2072909.
   Web of Science ®Google Scholar
• Niyazi, S.; Pouramiri, B.; Rabiei, K. J. Mol. Struct. 2022, 1250, 131908. DOI: 10.1016/j.molstruc.2021.131908.
   Web of Science ®Google Scholar
• Anary-Abbasinejad, M.; Anaraki-Ardakani, H.; Saidipoor, A.; Shojaee, M. J. Chem. Res. 2007, 535–537.
   Web of Science ®Google Scholar
• Anary-Abbasinejad, M.; Anaraki-Ardakani, H.; Hassanabadi, A. Synth. Commun. 2008, 38, 3706–3716. DOI: 10.1080/00397910802213778.
   Web of Science ®Google Scholar
• Malekpour, M.; Anaraki-Ardakani, H.; Noei, M. J. Chem. Res. 2012, 36, 715–717. DOI: 10.3184/174751912X13518648205073.
   Web of Science ®Google Scholar
• Asadi, H.; Anaraki-Ardakani, H.; Torabi, P.; Taheri, N. Rev. Roum. Chim. 2020, 65, 795–800. DOI: 10.33224/rrch.2020.65.9.05.
   Web of Science ®Google Scholar
• Asadi, H.; Anaraki-Ardakani, H.; Torabi, P.; Taheri, N. J. Appl. Chem. Res. 2022, 16, 48–56.
   Google Scholar
• Khodabakhshi, S.; Karami, B. Tetrahedron Lett. 2014, 55, 7136–7139. DOI: 10.1016/j.tetlet.2014.11.016.
   Web of Science ®Google Scholar
• Anaraki-Ardakani, H.; Charooseai, A. Orient. J. Chem. 2015, 31, 1455–1460. DOI: 10.13005/ojc/310324.
   Google Scholar
• Anaraki-Ardakani, H.; Zaki, E. Indian J. Fundam. Appl. Life Sci 2015, 15, 5421–5427.
   Google Scholar
• Khodabakhshi, S.; Khaleghi Abbasabadi, M.; Baghrnejad, M.; Marahel, F. J. Chin. Chem. Soc. 2015, 62, 9–12. DOI: 10.1002/jccs.201400266.
   Web of Science ®Google Scholar
• Khodabakhshi, S.; Khaleghi Abbasabadi, M.; Heydarian, S.; Gharehzadeh Shirazi, S.; Marahel, F. LOC 2015, 12, 465–470. DOI: 10.2174/1570178612666150331204620.
   Web of Science ®Google Scholar
• Khodabakhshi, S.; Karami, B.; Eskandari, K. Res. Chem. Intermed. 2015, 41, 7263–7272. DOI: 10.1007/s11164-014-1810-7.
   Web of Science ®Google Scholar
• Arfavi-Safari, M.; Anaraki-Ardakani, H.; Badri, R.; Tahanpesar, E. J. Chem. Res. 2017, 41, 321–324. DOI: 10.3184/174751917X14944355549131.
   Web of Science ®Google Scholar
• Arfavi-Safari1, M.; Anaraki-Ardakani, H.; Badri, R.; Tahanpesar, E. J. Appl. Chem. Res. 2019, 13, 27–40.
   Google Scholar
• Kiani, M.; Anaraki-Ardakani, H.; Hasanzadeh, N.; Rayatzadeh, A. Polycycl. Aromat. Compd. 2022. DOI: 10.1080/10406638.2022.2078377.
   Web of Science ®Google Scholar