References
- Vita-Finzi, P. The Chemistry of Heterocyclic Compounds; Wiley and Sons: New York, 1991; 4, part-1, p 417.
- Nauduri, D.; Reddy, G. B. Chem. Pharma. Bull. 1998, 46, 1254. https://doi.org/10.1248/cpb.46.1254
- Hoffer, M., US Patent, 2721200, 1995.
- Havrylyuk, D.; Zimenkovsky, B.; Vasylenko, O.; Zaprutko, L.; Lesyk, R. Eur. J. Med. Chem. 2009, 44, 1396. https://doi.org/10.1016/j.ejmech.2008.09.032
- Chiminchi, S.; Boccalini, M.; Hassan, M. M.; Viola, G.; Dall, A. F.; Curini, M. Tetrahedron 2006, 62, 90. https://doi.org/10.1016/j.tet.2005.09.135
- Korgaokar, S. S.; Patil, P. H.; Shah, M. J.; Parekh, H. H. Indian J. Pharm. Sci. 1996, 58, 222-225.
- Abid, M.; Bhat, A. R.; Athar, F.; Azam, A. Eur. J. Med. Chem. 2009, 44, 417. https://doi.org/10.1016/j.ejmech.2007.10.032
- Nugent, R. A.; Murphy, M.; Schlachter, S. T.; Dunn, C. J.; Smith, J. R.; Staite, N. D.; Galinet, A. L.; Asar, D. G.; Richard, K. A. J. Med. Chem. 1993, 36, 134. https://doi.org/10.1021/jm00053a017
- Manna, F.; Chimenti, F.; Balasco, A.; Cenicola, M. L.; Amico, M.; Parrilo, C.; Rossi, F.; Marmo, E. Eur. J. Med. Chem. 1992, 27, 633. https://doi.org/10.1016/0223-5234(92)90142-N
- Taylor, J.; Chandler, R.; Stauffer, J.; Harold, F., US Patent 4871737, 1989.
- Uno, H.; Kurokawa, M.; Masuda, Y.; Nishimura, H. J. Med. Chem. 1979, 22, 180. https://doi.org/10.1021/jm00188a011
- Taylor, E. S.; Patel, H. H. Tetrahedron 1992, 48, 8089. https://doi.org/10.1016/S0040-4020(01)80479-8
- Palaska, E.; Aytemir, M.; Uzbay, I. T.; Erol, D. Eur. J. Med. Chem. 2001, 36, 539. https://doi.org/10.1016/S0223-5234(01)01243-0
- Soliman, R.; Suzan, A. S.; Darwish, O. J. Med. Chem. 1983, 26(11), 1659. https://doi.org/10.1021/jm00365a023
- Hong, W. L.; Joong, B. A.; Sung, K. K.; Soon, K. A.; Deok, C. H. Org. Proc. Res. & Dev. 2007, 11, 190. https://doi.org/10.1021/op060087u
- Momura, M.; Kinoshita, S.; Satoh, H.; Maeda, T.; Murakami, K.; Tsunodam, M.; Miyachi, H.; Awano, K. Bioorg. Med. Chem. Lett. 1999, 9, 533. https://doi.org/10.1016/S0960-894X(99)00039-6
- Lewis, J. R. Nat. Prod. Rep. 1999, 16, 389. https://doi.org/10.1039/a802500b
- Breslow, R. J. Am. Chem. Soc. 1958, 80, 3719. https://doi.org/10.1021/ja01547a064
- Youssef, M. S.; Ahmed, R. A.; Abbady, M. S.; Abdel-Mohsen, S. A. Monatsh Chem. 2008, 139, 553. https://doi.org/10.1007/s00706-007-0817-9
- Clemence, F.; Marter, O. L.; Delevalle, F., Benzoni, J.; Jouanen, A.; Jouquey, S.; Deraedt, M. R. J. Med. Chem. 1988, 31, 1453. https://doi.org/10.1021/jm00402a034
- Tsuji, K., Ishikawa, H. Bioorg. Med. Chem. Lett. 1994, 4, 1601. https://doi.org/10.1016/S0960-894X(01)80574-6
- Li, J. T.; Zhang, X. H.; Lin, Z. P. Beilst. J. Org. Chem. 2007, 3, 13. https://doi.org/10.1186/1860-5397-3-13
- Molteni, V.; Hamilton, M. M.; Mao, L.; Crane, C. M.; Termin, A. P.; Wilson, D. M. Synthesis 2002, 12, 1669.
- Rajora, J.; Yadav, J.; Kumar, R.; Srivastava, Y. K. Indian J. Chem. 2010, 49, 989. https://doi.org/10.1021/ie900675d
- Kidwai, M.; Kukreja, S.; Thakur, R. Lett. Org. Chem. 2006, 3, 135. https://doi.org/10.2174/157017806775224170
- H3PW12Fazaeli, R.; Aliyan, H.; Bordbar, M.; Mohammadi, E. The Open Catly. J. 2010, 3, 79. https://doi.org/10.2174/1876214X01003010079
- Fringuelli, F.; Piermatti, O.; Pizzo, F. J. Chem. Educ. 2004, 81, 874. https://doi.org/10.1021/ed081p874
- Anastas, P. T.; Warner, J. C. Green Chem. Theory and Practice; Oxford University Press: New York, 1998.
- Heravi, M. M.; Baghernejad, B.; Oskooie, H. A. Mol. Diversity 2009, 13, 385. https://doi.org/10.1007/s11030-009-9122-3
- Grieco, P. A. Org. Synthes. In Water, Blackie Academic & Professional; London, 1998.
- Li, C. J.; Chang, T. H. Organic Reactions in Aqueous Media; Wiley: New York, 1997.
- Matlack, A. S. Introduction to Green Chem.; Marcel Dekker, Inc.: New York, 2001.
- Dallinger, D.; Kappe, C. O. Chem. Rev. 2007, 107, 2563. https://doi.org/10.1021/cr0509410
- Grieco, P. A. Organic Synthesis in Water; Blackie: London, 1998.
- Breslow, R. Acc. Chem. Res. 2004, 37, 471. https://doi.org/10.1021/ar040001m
- Azizi, N.; Aryanasab, F.; Torkiyan, L.; Ziyaei, A.; Saidi, M. R. J. Org. Chem. 2006, 71, 3634. https://doi.org/10.1021/jo060048g
- Tiwari, S.; Kumar, A. Angew. Chem. 2006, 118, 4942. Angew. Chem. Int. Ed. 2006, 45, 4824. https://doi.org/10.1002/anie.200600426
- Jung, Y.; Marcus, R. A. J. Am. Chem. Soc. 2007, 129, 5492. https://doi.org/10.1021/ja068120f
- Fendler, J. H.; Fendler, E. J. Catalysis in Micellar and Macromolecular Systeams; Academic Press: London, 1975.
- Manabe, K.; Sun, X. M.; Kobayashi, S. J. Am. Chem. Soc. 2001, 123, 10101. https://doi.org/10.1021/ja016338q
- Shinde, P. V.; Kategaonkar, A. H.; Shingate, B. B.; Shingare, M. S. Beilst. J. Org. Chem. 2011, 7, 53. https://doi.org/10.3762/bjoc.7.9
- Shiri, M.; Zolfigol, M. A. Tetrahedron 2009, 65, 587. https://doi.org/10.1016/j.tet.2008.09.085
- Dandia, A.; Singh, R.; Bhaskaran, S.; Sarriant, S. D. Green Chem. 2011, DOI: 10.1039/c0gc00863.
- Jawale, D. V.; Pratap, U. R.; Rahuja, N.; Srivastava, A. K.; Mane, R. A. Bioorg. Med. Chem. Lett. 2012, 22, 436-439. https://doi.org/10.1016/j.bmcl.2011.10.110
- Pratap, U. R.; Jawale, D. V.; Waghmare, R. A.; Lingampalle, D. L.; Mane, R. A. New J. Chem. 2011, 35, 49. https://doi.org/10.1039/c0nj00691b
- Mali, J. R.; Bhosle, M. R.; Mahalle, S. R.; Mane, R. A. Bull. Korean Chem. Soc. 2010, 31, 1859. https://doi.org/10.5012/bkcs.2010.31.7.1859
- Bazargan, L.; Shafiee, A.; Amini, M.; Defouli, E. B.; Azizi, E.; Ghaffari, S. M. Phosph, Sulf. & Silicon 2009, 184, 602. https://doi.org/10.1080/10426500802239529
- Mahmoodi, M.; Aliabadi, A.; Emami, S.; Safavi, M.; Rajabalian, S.; Mohagheghi, M. A.; Khoshzaban, A.; Kermani, A. S.; Lamei, N.; Shafiee, A.; Foroumadi, A. Arch. Pharm. Chem. Life. Sci. 2010, 343, 411. https://doi.org/10.1002/ardp.200900198
- Wang, L. M.; Jiao, N.; Qiu, J.; Yu, J. J.; Liu, J. Q.; Guo, F. L.; Liu, Y. Tetrahedron 2010, 1, 339.
- Watanabe, Y.; Sawada, K.; Hayashi, M. Green Chem. 2010, 12, 384. https://doi.org/10.1039/b918349c
- Firouzabadi, H.; Iranpoor, N.; Garzan, A. Adv. Synth. Catal. 2005, 347, 1925. https://doi.org/10.1002/adsc.200505222
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