References
- Suslick, K. S.; Hammerton, D. A.; Cline, R. E. J. Am. Chem. Soc. 1986, 108, 5641–5642. DOI: https://doi.org/10.1021/ja00278a055.
- (a) Singh, B. S.; Lobo, H. R.; Pinjari, D. V.; Jarag, K. J.; Pandit, A. B.; Shankarling, G. S. Ultrason. Sonochem. 2013, 20, 287–293. DOI: https://doi.org/10.1016/j.ultsonch.2012.06.003. (b) Puri, S.; Kaur, B.; Parmar, A.; Kumar, H. COC 2013, 17, 1790–1828. DOI: https://doi.org/10.2174/13852728113179990018.
- Cintas, P.; Luche, J. L. Green Chem. 1999, 1, 115–125. DOI: https://doi.org/10.1039/a900593e.
- (a) Machado, P.; Lima, G. R.; Rotta, M.; Bonacorso, H. G.; Zanatta, N.; Martins, M. A. P. Ultrason. Sonochem. 2011, 18, 293–299. DOI: https://doi.org/10.1016/j.ultsonch.2010.06.009. (b) Santos, C. R.; Echevarria, A. Tetrahedron. Lett. 2011, 52, 336–340. DOI: https://doi.org/10.1016/j.tetlet.2010.11.054. (c) Gouvea, D. P.; Duval, A. R.; Drawanz, B. B.; Rosales, P. F.; Gomes, C. R. B.; Pereira, C. M. P.; Cunico, W. Ultrason. Sonochem. 2011, 18, 65. (d) Bretanha, L. C.; Teixeira, V. E.; Ritter, M.; Siqueira, G. M.; Cunico, W.; Pereira, C. P. M.; Freitag, R. A. Ultrason. Sonochem. 2011, 18, 704–707. DOI: https://doi.org/10.1016/j.ultsonch.2010.09.016. (e) Buriol, L.; Munchen, T. S.; Frizzo, C. P.; Marzari, M. R. B.; Zanatta, N.; Bonacorso, H. G.; Martins, M. A. P. Ultrason. Sonochem. 2013, 20, 1139–1143. DOI: https://doi.org/10.1016/j.ultsonch.2013.02.006. (f) Li, D.; Zang, H.; Changchun, W.; Nianqin, Y. Ultrason. Sonochem. 2013, 20, 1144–1148. DOI: https://doi.org/10.1016/j.ultsonch.2013.01.019. (g) Safari, J.; Zarnegar, Z. Ultrason. Sonochem. 2013, 20, 740–746. DOI: https://doi.org/10.1016/j.ultsonch.2012.10.004.
- (a) Masters, J. J.; Link, J. T.; Snyder, L. B.; Young, W. B.; Danishefsky, S. J. Angew. Chem. 1995, 107, 1886–1888. DOI: https://doi.org/10.1002/ange.19951071617. (b) Masters, J. J.; Link, J. T.; Snyder, L. B.; Young, W. B.; Danishefsky, S. J. Angew. Chem. Int. Ed. Engl. 1995, 34, 1723–1726. DOI: https://doi.org/10.1002/anie.199517231.
- (a) Organic Synthesis, John Wiley and Sons: New York, 1999. (b) Kocienski, P. J. In Protecting Groups, Georg Thieme: New York, 2000. (c) Schelhaas, M.; Waldmann, H. Angew. Chem. Int. Ed. Engl. 1996, 35, 2056–2083. DOI: https://doi.org/10.1002/anie.199620561. (d) Wuts, P. G. M.; Greene, T. W. Greene’s Protective Groups in Organic Synthesis, John Wiley and Sons, NewYork, NY, USA, 4th edition, 2007. (e) Isidro-Llobet, A.; Alvarez, M.; Albericio, F. Chem. Rev. 2009, 109, 2455–2504.
- Sartori, G.; Ballini, R.; Bigi, F.; Bosica, G.; Maggi, R.; Righi, P. Chem. Rev. 2004, 104, 199–250. DOI: https://doi.org/10.1021/cr0200769.
- (a) Carpino, L. A.; Parameswaran, K. N.; Kirkley, R. K.; Spiewak, J. W.; Schmitz, E. J. Org. Chem. 1970, 35, 3291–3295. DOI: https://doi.org/10.1021/jo00835a025. (b) Dieter, R. K.; Dieter, J. W.; Alexander, C. W.; Bhinderwala, N. S. J. Org. Chem. 1996, 61, 2930–2931. DOI: https://doi.org/10.1021/jo960272d. (c) Burkhart, F.; Hoffmann, M.; Kessler, H. Angew. Chem. Int. Ed. Engl. 1997, 36, 1191–1192. DOI: https://doi.org/10.1002/anie.199711911. (d) Kaiser, E. S.; Picart, F.; Kubiak, T.; Tam, J. P.; Merrifield, R. B. J. Org. Chem. 1993, 58, 5167–5175. DOI: https://doi.org/10.1021/jo00071a028. (e) Xiao, X. Y.; Ngu, K.; Chao, C.; Petal, D. V. J. Org. Chem. 1997, 62, 6968. DOI: https://doi.org/10.1021/jo971087i.
- (a) Burk, M. J.; Allen, J. G. J. Org. Chem. 1997, 62, 7054–7057. DOI: https://doi.org/10.1021/jo970903j. (b) Basel, Y.; Hassner, A. J. Org. Chem. 2000, 65, 6368–6380. DOI: https://doi.org/10.1021/jo000257f. (c) Kelly, T. A.; McNeil, D. W. A. Tetrahedron Lett. 1994, 35, 9003–9006. DOI: https://doi.org/10.1016/0040-4039(94)88411-0. (d) Barcelo, G.; Senet, J.-P.; Sennyey, G.; Bensoam, J.; Loffet, A. Synthesis 1986, 1986, 627–632. DOI: https://doi.org/10.1055/s-1986-31724. (e) Lutz, C.; Lutz, V.; Knochel, P. Tetrahedron 1998, 54, 6385–6402. DOI: https://doi.org/10.1016/S0040-4020(98)00297-X. (f) Bailey, S. W.; Chandrasekaran, R. Y.; Ayling, J. E. J. Org. Chem. 1992, 57, 4470–4477. DOI: https://doi.org/10.1021/jo00042a030. (g) Itoh, M.; Hagiwara, D.; Kamiya, T. Tetrahedron Lett. 1975, 16, 4390. (h) Kelly, T. A.; McNeil, D. W. Tetrahedron Lett. 1994, 35, 9003–9006. DOI: https://doi.org/10.1016/0040-4039(94)88411-0. (i) Khaligh, N. G. RSC Adv. 2012, 2, 12364. DOI: https://doi.org/10.1039/c2ra20905e. (j) Feldman, K. S.; Ngernmeesri, P. Org. Lett. 2010, 12, 4502–4505. DOI: https://doi.org/10.1021/ol1018008. (k) Rahman, M. M.; Li, G.; Szostak, M. J. Org. Chem. 2019, 84, 12091–12100. DOI: https://doi.org/10.1021/acs.joc.9b02013.
- (a) Sharma, G. V. M.; Reddy, J. J.; Lakshmi, P. S.; Krishna, P. R. Tetrahedron Lett. 2004, 45, 6963–6965. DOI: https://doi.org/10.1016/j.tetlet.2004.07.072. (b) Bartoli, G.; Bosco, M.; Locatelli, M.; Marcantoni, E.; Massaccesi, M.; Melchiorre, P.; Sambri, L. Synlett 2004, 2004, 1794–1798. DOI: https://doi.org/10.1055/s-2004-829059. (c) Heydari, A.; Hosseini, S. E. Adv. Synth. Catal. 2005, 347, 1929–1932. DOI: https://doi.org/10.1002/adsc.200505218. (d) Rajanna, K. C. Synth. Commun. 2011, 41, 715. (e) Chankeshwara, S. V.; Chakraborti, A. K. Tetrahedron Lett. 2006, 47, 1087–1091. DOI: https://doi.org/10.1016/j.tetlet.2005.12.044. (f) Suryakiran, N.; Prabhakar, P.; Reddy, T. S.; Rajesh, K.; Venkateswarlu, Y. Tetrahedron Lett. 2006, 47, 8039–8042. DOI: https://doi.org/10.1016/j.tetlet.2006.09.081. (g) Suryakiran, N.; Prabhakar, P.; Reddy, T. S.; Srinivasulu, M.; Swamy, N. R.; Venkateswarlu, Y. J. Mol. Catal. A: Chem. 2007, 264, 40–43. DOI: https://doi.org/10.1016/j.molcata.2006.09.005. (h) Chankeshwara, S. V.; Chakraborti, A. K. Synthesis 2006, 2006, 2784–2788. DOI: https://doi.org/10.1055/s-2006-942492. (i) Inahashi, N.; Matsumiya, A.; Sato, T. Synlett 2008, 2008, 294–296. DOI: https://doi.org/10.1055/s-2007-1000869. (j) Varala, R.; Nuvula, S.; Adapa, S. R. J. Org. Chem. 2006, 71, 8283–8286. DOI: https://doi.org/10.1021/jo0612473. (k) Shailaja, M.; Manjula, A.; Rao, B. V. Synth. Commun. 2011, 41, 2073–2080. DOI: https://doi.org/10.1080/00397911.2010.497592. (l) Heydari, A.; Khaksar, S.; Tajbakhsh, M.Synthesis 2008, 2008, 3126–3130. DOI: https://doi.org/10.1055/s-2008-1067272. (m) Shirini, F.; Zolfigol, M. A.; Abedini, M. JICS 2010, 7, 603–607. DOI: https://doi.org/10.1007/BF03246047. (n) Shirini, F.; Khaligh, N. G. Monatsh. Chem. 2012, 143, 631–635. DOI: https://doi.org/10.1007/s00706-011-0612-5. (o) Schechter, A.; Doldrich, D.; Chapman, J. R.; Uberheide, B. M.; Lim, D. Synth. Commun. 2015, 43, 643.
- (a) Knolker, H. J.; Braxmeier, T.; Schlechtingen, G. Synlett 1996, 1996, 502–504. DOI: https://doi.org/10.1055/s-1996-5472. (b) Knolker, H. J.; Braxmeier, T. Tetrahedron Lett. 1996, 37, 5861–5864. DOI: https://doi.org/10.1016/0040-4039(96)01248-8. (c) Knolker, H. J.; Braxmeier, T.; Schlechtingen, G. Angew. Chem. Int. Ed. Engl. 1995, 34, 2497–2500. DOI: https://doi.org/10.1002/anie.199524971. (d) Darnbrough, S.; Mervic, M.; Condon, S. M.; Burns, C. J. Synth. Commun. 2001, 31, 3273–3280. DOI: https://doi.org/10.1081/SCC-100106036.
- (a) Zolfigol, M. A.; Khakyzadeh, V.; Moosavi-Zare, A. R.; Chehardoli, G.; Derakhshan-Panah, F.; Zare, A.; Khaledian, O. ScientiaIranica 2012, 19, 1584. (b) Chinnappan, A.; La, D.; Kim, H. RSC Adv. 2013, 3, 13324. DOI: https://doi.org/10.1039/c3ra40778k. (c) Karimian, S.; Tajik, H. Chinese Chemical Lett. 2014, 25, 218–220. DOI: https://doi.org/10.1016/j.cclet.2013.11.052. (d) Majumdar, S.; De, J.; Chakraborty, A.; Maiti, D. K. RSC Adv. 2014, 4, 24544. DOI: https://doi.org/10.1039/c4ra02670e. (e) Shirini, F.; Jolodar, O. G.; Seddighi, M.; Borujeni, H. T. RSC Adv. 2015, 5, 19790–19798. DOI: https://doi.org/10.1039/C4RA14130J. (f) Koodehi, T. G.; Shirini, F.; Goli-Jolodar, O. J. Iran. Chem. Soc. 2017, 14, 443–456. DOI: https://doi.org/10.1007/s13738-016-0992-x. (g) Azizi, N.; Shirdel, F. Monatsh. Chem. 2017, 148, 1069–1074. 6, DOI: https://doi.org/10.1007/s00706-016-1856-x. (h) Reddy, M. S.; Narender, M.; Nageswar, Y. V. D.; Rao, K. R. Synlett 2006, 2006, 1110–1112. DOI: https://doi.org/10.1055/s-2006-939689.
- (a) Chantarasriwong, O.; Jiangchareon, B.; Putra, C. K.; Suwankrua, W.; Chavasiri, W. Tetrahedron Lett. 2016, 57, 4807–4811. DOI: https://doi.org/10.1016/j.tetlet.2016.09.052. (b) Kumar, K. S.; Iqbal, J.; Pal, M. Tetrahedron Lett. 2009, 50, 6244–6246. DOI: https://doi.org/10.1016/j.tetlet.2009.09.018. (c) Das, B.; Venkateswarlu, K.; Krishnaiah, M.; Holla, H. Tetrahedron Lett. 2006, 47, 7551–7556. DOI: https://doi.org/10.1016/j.tetlet.2006.08.093. (d) Atghia, S. V.; SarviBeigbaghlou, S. J. Organomet. Chem. 2013, 745, 42. (e) Shirini, F.; Mamaghani, M.; Atghia, S. V. Catal. Commun. 2011, 12, 1088–1094. DOI: https://doi.org/10.1016/j.catcom.2011.03.030. (f) Heydari, A.; Shiroodi, R. K.; Hamadi, H.; Esfandyari, M.; Pourayoubi, M. Tetrahedron Lett. 2007, 48, 5865–5868. DOI: https://doi.org/10.1016/j.tetlet.2007.06.064. (g) Chankeshwara, S. V.; Chakraborti, A. K. J. Mol. Catal. A: Chem. 2006, 253, 198–202. DOI: https://doi.org/10.1016/j.molcata.2006.03.042. (h) Veisi, H.; Sedrpoushan, A.; Ghazizadeh, H.; Hemmati, S. Res. Chem. Intermed. 2016, 42, 1451–1461. DOI: https://doi.org/10.1007/s11164-015-2096-0. (i) Karmakar, B.; Banerji, J. Tetrahedron Lett. 2010, 51, 3855–3858. DOI: https://doi.org/10.1016/j.tetlet.2010.05.080. (j) Chakraborti, A. K.; Chankeshwara, S. V. Org. Biomol. Chem. 2006, 4, 2769–2771. DOI: https://doi.org/10.1039/b605074c. (k) Khaligh, N. G.; Hazarkhani, H. Monatsh. Chem. 2014, 145, 1975–1980. DOI: https://doi.org/10.1007/s00706-014-1274-x. (l) Shirini, F.; Atghia, S. V.; Jirdehi, M. G. Chin. Chem. Lett. 2013, 24, 34. (m) Zolfigol, M. A.; Moosavi-Zare, A. R.; Moosavi, P.; Khakyzadeh, V.; Zare, A. C. R. Chim. 2013, 16, 962–966. DOI: https://doi.org/10.1016/j.crci.2013.05.010. (n) Chaskar, A.; Yewale, S.; Langi, B.; Deokar, H. J. Korean Chem. Soc. 2009, 53, 422. (o) Khaksar, S.; Vahdat, S. M.; Tajbakhsh, M.; Jahani, F.; Heydari, A. Tetrahedron Lett. 2010, 51, 6388–6391. DOI: https://doi.org/10.1016/j.tetlet.2010.09.096. (p) Jahani, F.; Tajbakhsh, M.; Golchoubian, H.; Khaksar, S. Tetrahedron Lett. 2011, 52, 1260–1264. DOI: https://doi.org/10.1016/j.tetlet.2011.01.023. (q) Upadhyaya, D. J.; Barge, A.; Stefania, R.; Cravotto, G. Tetrahedron Lett. 2007, 48, 8318–8322. DOI: https://doi.org/10.1016/j.tetlet.2007.09.126. (r) Sunitha, S.; Kanjilal, S.; Reddy, P. S.; Prasad, R. B. N. Tetrahedron Lett. 2008, 49, 2527–2532. DOI: https://doi.org/10.1016/j.tetlet.2008.02.126. (s) Ingale, A. P.; Ukale, D.; Garad, D. N.; Shinde, S. V. Synth. Commun. 2021, 51, 1656. (t) Ingale, A. P.; Shinde, S. V.; Thorat, N. M. Synth. Commun. 2021, 51, 2528–2543. DOI: https://doi.org/10.1080/00397911.2021.1942060.
- (a) Chankeshwara, S. V.; Chakraborti, A. K. Org. Lett. 2006, 8, 3259–3262. DOI: https://doi.org/10.1021/ol0611191. (b) Vilaivan, T. Tetrahedron Lett. 2006, 47, 6739–6742. DOI: https://doi.org/10.1016/j.tetlet.2006.07.097. (c) Siddaiah, V.; Basha, G. M.; Rao, G. P.; Prasad, U. V.; Rao, R. S. Chem. Lett. 2010, 39, 1127–1129. DOI: https://doi.org/10.1246/cl.2010.1127. (d) Zeng, H.; Li, Y.; Shao, H. Synth. Commun. 2012, 42, 25–32. DOI: https://doi.org/10.1080/00397911.2010.520831. (e) Jia, X.; Huang, Q.; Li, J.; Li, S.; Yang, Q. Synlett 2007, 2007, 0806–0808. DOI: https://doi.org/10.1055/s-2007-970755. (f) Dighe, S. N.; Jadhav, H. R. Tetrahedron Lett. 2012, 53, 5803–5806. DOI: https://doi.org/10.1016/j.tetlet.2012.08.089. (g) Nardi, M.; Cano, N. H.; Costanzo, P.; Oliverio, M.; Sindona, G.; Procopio, A. RSC Adv. 2015, 5, 18751–18760. DOI: https://doi.org/10.1039/C4RA16683C. (h) Khaksar, S.; Heydari, A.; Tajbakhsh, M.; Vahdat, S. M. Tetrahedron Lett. 2008, 49, 3527–3529. DOI: https://doi.org/10.1016/j.tetlet.2008.03.138. (i) Ingale, A. P.; More, V. K.; Gangarde, U. S.; Shinde, S. V. New J. Chem. 2018, 42, 10142–10147.
- (a) Khatri, C. K.; Rekunge, D. S.; Chaturbhuj, G. U. New J. Chem. 2016, 40, 10412–10417. DOI: https://doi.org/10.1039/C6NJ03120J. (b) Khatri, C. K.; Satalkar, V. B.; Chaturbhuj, G. U. Tetrahedron Lett. 2017, 58, 694–698. DOI: https://doi.org/10.1016/j.tetlet.2017.01.022. (c) Rekunge, D. S.; Khatri, C. K.; Chaturbhuj, G. U. Tetrahedron Lett. 2017, 58, 1240–1244. DOI: https://doi.org/10.1016/j.tetlet.2017.02.038. (d) Indalkar, K. S.; Khatri, C. K.; Chaturbhuj, G. U. J. Chem. Sci. 2017, 129, 141–148. DOI: https://doi.org/10.1007/s12039-017-1235-0. (e) Indalkar, K. S.; Khatri, C. K.; Chaturbhuj, G. U. J. Chem. Sci. 2017, 129, 415–420. DOI: https://doi.org/10.1007/s12039-017-1257-7. (f) Khatri, C. K.; Patil, M. S.; Chaturbhuj, G. U. J. Iran. Chem. Soc. 2017, 14, 1683–1689. DOI: https://doi.org/10.1007/s13738-017-1109-x. (g) Khatri, C. K.; Mali, A. S.; Chaturbhuj, G. U. Monatsh. Chem. 2017, 148, 1463–1468. DOI: https://doi.org/10.1007/s00706-017-1944-6. (h) Indalkar, K. S.; Khatri, C. K.; Chaturbhuj, G. U. Tetrahedron Lett. 2017, 58, 2144–2148. DOI: https://doi.org/10.1016/j.tetlet.2017.04.058. (i) Patil, M. S.; Palav, A. V.; Khatri, C. K.; Chaturbhuj, G. U. Tetrahedron Lett. 2017, 58, 2859–2864. DOI: https://doi.org/10.1016/j.tetlet.2017.06.027. (j) Patil, M. S.; Mudaliar, C.; Chaturbhuj, G. U. Tetrahedron Lett. 2017, 58, 3256–3261. DOI: https://doi.org/10.1016/j.tetlet.2017.07.019. (k) Rekunge, D. S.; Khatri, C. K.; Chaturbhuj, G. U. Monatsh. Chem. 2017, 148, 2091–2095. DOI: https://doi.org/10.1007/s00706-017-2013-x. (l) Khatri, C. K.; Chaturbhuj, G. U.; Iran, J. Chem. Soc. 2017, 14, 2513. (m) Rekunge, D. S.; Khatri, C. K.; Chaturbhuj, G. U. Tetrahedron Lett. 2017, 58, 4304–4307. DOI: https://doi.org/10.1016/j.tetlet.2017.10.001.