References
- Anastas, P. T.; Kirchhoff, M. M. Acc. Chem. Res. 2002, 35, 686. https://doi.org/10.1021/ar010065m
- Sheldon, R. A. Green Chem. 2005, 7, 267. https://doi.org/10.1039/b418069k
- Nuchter, M.; Ondruschka, B.; Jungnickel, A.; Muller, U. J. Phys. Org. Chem. 2000, 13, 579. https://doi.org/10.1002/1099-1395(200010)13:10<579::AID-POC272>3.0.CO;2-M
- Varma, R. S. Green Chem. 2008, 10, 1129 https://doi.org/10.1039/b817559b
- Mason, T. J. Chem. Soc. Rev. 1997, 26, 443. https://doi.org/10.1039/cs9972600443
- Luche, J. L. Synthetic Organic Sonochemistry; Plenum Press: New York, 1998.
- Mason, T. J. Advances in Sonochemistry; JAI Press: London and Greenwich, CT, 1990.
- Mason, T. J.; Lorimer, J. P. Chem. Soc. Rev. 1987, 16, 239. https://doi.org/10.1039/cs9871600239
- Li, J. T.; Wang, S. X.; Chen, G. F.; Li, T. S. Curr. Org. Synth. 2005, 2, 415. https://doi.org/10.2174/1570179054368509
- Cravotto, G.; Cintas, P. Chem. Soc. Rev. 2006, 35, 180. https://doi.org/10.1039/b503848k
- Cella, R.; Stefani, H. Tetrahedron 2009, 65, 2619. https://doi.org/10.1016/j.tet.2008.12.027
- Mason, T. J.; Cintas, P. In Handbook of Green Chemistry and Technology; Clark, J., Macquarrie, D., Eds.; Blackwell Science: Oxford, 2002.
- Schutz, H. Benzodiazepines; Springer: Heidelberg, 1982.
- Landquist, J. K. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Rees, C. W., Eds.; Pergamon: Oxford, 1984.
- Randall, L. O.; Kappel, B. In Benzodiazepines; Garattini, S., Mussini, E., Randall, L. O., Eds.; Raven Press: New York, 1973.
- Essaber, M.; Baouid, A.; Hasnaoui, A.; Benharref, A.; Lavergne, J. P. Synth. Commun. 1998, 28, 4097. https://doi.org/10.1080/00397919809458689
- Xu, J. X.; Wu, H. T.; Jin, S. Chin. J. Chem. 1999, 17, 84.
- Zhang, X. Y.; Xu, J. X.; Jin, S. Chin. J. Chem. 1999, 17, 404.
- Reddy, K. V. V.; Rao, P. S.; Ashok, D. Synth. Commun. 2000, 30, 1825. https://doi.org/10.1080/00397910008087228
- Zhang, W.; Williams, J. P.; Lu, Y.; Nagashima, T.; Chu, Q. Tetrahedron Lett. 2007, 48, 563. https://doi.org/10.1016/j.tetlet.2006.11.127
- Ried, W.; Torinus, E. Chem. Ber. 1959, 92, 2902. https://doi.org/10.1002/cber.19590921138
- Herbert, J. A. L.; Suschitzky, H. J. Chem. Soc.: Perkin Trans. 1 1974, 2657. https://doi.org/10.1039/p19740002657
- Jung, D. I.; Choi, T. W.; Kim, Y. Y.; Kim, I. S.; Park, Y. M.; Lee, Y. G.; Jung, D. H. Synth. Commun. 1999, 29, 1941. https://doi.org/10.1080/00397919908086183
- Sabitha, G.; Reddy, G. S.; Reddy, K. B.; Reddy, N. M.; Yadav, J. S. Adv. Synth. Catal. 2004, 346, 921. https://doi.org/10.1002/adsc.200303196
- Bandgar, B. P.; Bettigeri, S. V.; Joshi, N. S. Synth. Commun. 2004, 34, 1447. https://doi.org/10.1081/SCC-120030695
- Chen, W. Y.; Lu, J. Synlett 2005, 8, 1337.
- Pasha, M. A.; Jayashankara, V. P. Heterocycles 2006, 68, 1017. https://doi.org/10.3987/COM-05-10647
- Luo, Y. Q.; Xu, F.; Han, X. Y.; Shen, Q. Chin. J. Chem. 2005, 23, 1417. https://doi.org/10.1002/cjoc.200591417
- Wu, J. T.; Xu, F.; Zhou, Z. Q.; Shen, Q. Synth. Commun. 2006, 36, 457. https://doi.org/10.1080/00397910500383527
- Balakrishna, M. S.; Kaboundin, B. Tetrahedron Lett. 2001, 42, 1127. https://doi.org/10.1016/S0040-4039(00)02168-7
- Yadav, J. S.; Reddy, B. V. S.; Eshwaraian, B.; Anuradha, K. Green Chem. 2002, 4, 592. https://doi.org/10.1039/b206558b
- Curini, M.; Epifano, F.; Marcotullio, M. C.; Rosati, O. Tetrahedron Lett. 2001, 42, 3193. https://doi.org/10.1016/S0040-4039(01)00413-0
- Pan, X. Q.; Zou, J. P.; Huang, Z. H.; Zhang, W. Tetrahedron Lett. 2008, 49, 5302. https://doi.org/10.1016/j.tetlet.2008.06.082
- Jiang, Y. J.; Cai, J. J.; Zou, J. P. Zhang, W. Tetrahedron Lett. 2010, 51, 471. https://doi.org/10.1016/j.tetlet.2009.11.049
- Kaboudin, B.; Navaee, K. Heterocycles 2001, 55, 1443. https://doi.org/10.3987/COM-01-9253
- Pozarentzi, M.; Stephanidou, S. J.; Tsoleridis, C. A. Tetrahedron Lett. 2002, 43, 1755. https://doi.org/10.1016/S0040-4039(02)00115-6
- Reddy, B. M.; Sreekanth, P. M. Tetrahedron Lett. 2003, 44, 4447. https://doi.org/10.1016/S0040-4039(03)01034-7
- Kuo, C. W.; More, S. V.; Yao, C. F. Tetrahedron Lett. 2006, 47, 8523. https://doi.org/10.1016/j.tetlet.2006.09.128
- Varala, R.; Enugala, R.; Nuvula, S.; Adapa, S. R. Synlett 2006, 7, 1009.
- An, L. T.; Ding, F. Q.; Zou, J. P.; Lu, X. H. Synth. Commun. 2008, 38, 1259. https://doi.org/10.1080/00397910701873243
- Yadav, J. S.; Reddy, B. V. S.; Praveenkumar, S.; Nagaiah, K.; Lingaiah, N.; Saiprasad, P. S. Synthesis 2004, 6, 901.
- Yadav, J. S.; Reddy, B. V. S.; Praveenkumar, S.; Nagaiah, K. Synthesis 2005, 3, 480.
- Du, Y. Y.; Tian, F. L.; Zhao, W. Z. Synth. Commun. 2006, 36, 1661. https://doi.org/10.1080/00397910600616602
- Guzen, K. P.; Cella, R.; Stefani, H. A. Tetrahedron Lett. 2006, 47, 8133. https://doi.org/10.1016/j.tetlet.2006.09.043
- Sharma, S. D.; Gogoi, P.; Konwar, D. Green Chem. 2007, 9, 153. https://doi.org/10.1039/b611327c
- Dalko, P. I.; Moisan, L. Angew. Chem. Int. Ed. 2004, 43, 5138. https://doi.org/10.1002/anie.200400650
- Makoto, M.; Yamamoto, H. Bull. Chem. Soc. Jpn. 1995, 68, 2657. https://doi.org/10.1246/bcsj.68.2657
- Gayet, A.; Bolea, C.; Andersson, P. G. Org. Biomol. Chem. 2004, 2, 1887. https://doi.org/10.1039/b402805h
- Gorityala, B. K.; Cai, S.; Ma, J.; Liu, X. W. Bioorg. Med. Chem. Lett. 2009, 19, 3093. https://doi.org/10.1016/j.bmcl.2009.04.003
- Barrett, A. G. M.; Braddock, D. C.; Christian, P. W. N.; Pilipauskas, D.; White, A. J. P.; Williams, D. J. J. Org. Chem. 1998, 63, 5818. https://doi.org/10.1021/jo980582r
- Sejin, O.; Gijung, K.; Narae, K.; Shim, S. E.; Soonja, C. Macromol. Res. 2005, 13, 187. https://doi.org/10.1007/BF03219051
- Sapkal, S. B.; Shelke, K. F.; Shingate, B. B.; Shingare, M. S. Tetrahedron Lett. 2009, 50, 1754. https://doi.org/10.1016/j.tetlet.2009.01.140
- Niralwad, K. S.; Shingate, B. B.; Shingare, M. S. Ultrason. Sonochem. 2010, 17, 760. https://doi.org/10.1016/j.ultsonch.2010.02.002
- Shinde, P. V.; Sonar, S. S.; Shingate, B. B.; Shingare, M. S. Tetrahedron Lett. 2010, 51, 1309. https://doi.org/10.1016/j.tetlet.2009.12.146
- Niralwad, K. S.; Shingate, B. B.; Shingare, M. S. Tetrahedron Lett. 2010, 51, 3616. https://doi.org/10.1016/j.tetlet.2010.04.118
- Loupy, A. Solvent-free Reactions In Modern Solvents In Organic Synthesis; Knochel, P., Ed.; Topics in Current Chemistry 1999, 206, 153.
- De La Guardia, M.; Salvador, A. Analytica Chimica Acta 1989, 224, 123. https://doi.org/10.1016/S0003-2670(00)83451-0
Cited by
- ChemInform Abstract: An Organocatalyzed and Ultrasound Accelerated Expeditious Synthetic Route to 1,5-Benzodiazepines under Solvent-Free Conditions. vol.42, pp.38, 2011, https://doi.org/10.1002/chin.201138169
- Synthesis of some new substituted oxiranes from 4′-hydroxy-3′,5′-dinitrochalcones and their sulfanilic acid-catalyzed aminolysis vol.40, pp.2, 2014, https://doi.org/10.1007/s11164-012-0982-2
- Synthesis of pyrrolidinone derivatives from aniline, an aldehyde and diethyl acetylenedicarboxylate in an ethanolic citric acid solution under ultrasound irradiation vol.18, pp.12, 2016, https://doi.org/10.1039/C6GC00157B
- β-Cyclodextrin as a Biomimetic Catalyst for the Efficient Synthesis of 4-Oxo-pyrido[1,2-a] Pyrimidine-3-Carbonitrile in Aqueous Medium vol.147, pp.3, 2017, https://doi.org/10.1007/s10562-017-1983-y
- Synthesis of six- and seven-membered heterocycles under ultrasound irradiation vol.48, pp.11, 2018, https://doi.org/10.1080/00397911.2018.1434894
- Ultrasound assisted the green synthesis of 2-amino-4H-chromene derivatives catalyzed by Fe3O4-functionalized nanoparticles with chitosan as a novel and reusable magnetic catalyst vol.22, pp.None, 2015, https://doi.org/10.1016/j.ultsonch.2014.02.002
- An efficient contemporary multicomponent synthesis for the facile access to coumarin‐fused new thiazolyl chromeno[4,3‐ b ]quinolones in aqueous micellar medium vol.57, pp.1, 2011, https://doi.org/10.1002/jhet.3802
- Ultrasound for Drug Synthesis: A Green Approach vol.13, pp.2, 2011, https://doi.org/10.3390/ph13020023
- Iodine‐catalyzed ultrasound‐assisted construction of pyridines and their glutamine synthetase molecular docking vol.67, pp.7, 2011, https://doi.org/10.1002/jccs.201900389