One-pot access to new tetrahydrobenzo[a]xanthen-11-ones and naphthopyranopyrimidines using 2,3-dihydroxynaphthalene

References

• (a) Zhu, J.; Bienayme, H. (Eds.). Multicomponent Reactions; Wiley-VCH: Weinheim, 2005; (b) Ganem, B. Acc. Chem. Res. 2009, 42, 463–472 (c) Domling, A.; Ugi, I. Angew. Chem. Int. Ed. 2000, 39, 3169–3210.
   Google Scholar
• (a) Shaabani, A.; Maleki, A.; Rezayan, A. H.; Sarvary, A. J. Mol. Divers. 2011, 15, 41–68; (b) Altug, C.; Burnett, A. K.; Caner, E.; Durust, Y.; Elliott, M. C.; Glanville, R. P. J.; Guy, C.; Westwell, A. D. Tetrahedron 2011, 67, 9522–9528.
   PubMed Web of Science ®Google Scholar
• (a) Elinson, M. N.; Ilovaisky, A. I.; Merkulova, V. M.; Belyakov, P. A.; Chizhov, A. O. Tetrahedron 2010, 66, 4043–4048; (b) Dekamin, M. G.; Mokhtari, Z. Tetrahedron 2012, 68, 922–930; (c) Dekamin, M. G.; Mokhtari, Z.; Karimi, Z. Sci. Iran. Trans. C: Chem. Chem. Eng. 2011, 18, 1356–1364.
   Web of Science ®Google Scholar
• Wang, H.; Lu, L.; Zhu, S.; Li, Y. Cai, W. Curr. Microbiol. 2006, 52, 1–5.
   PubMed Web of Science ®Google Scholar
• Vennerstrom, J. L.; Makler, M. T.; Angerhofer, C. K.; Williams, J. A. Antimicrob. Agents Chemother. 1995, 39, 2671–2677.
   PubMed Web of Science ®Google Scholar
• Giri, R.; Goodell, J. R.; Xing, C. G. Bioorg. Med. Chem. 2000, 18, 1456–1463.
   Web of Science ®Google Scholar
• Chibale, K.; Visser, M.; Schalkwyk, D. V. Tetrahedron 2003, 59, 2289–2296.
   Web of Science ®Google Scholar
• Ahmad, M.; King, T. A.; Cha, B. H.; Lee, J. J. Phys. D: Appl. Phys. 2002, 35, 1473–1476.
   Web of Science ®Google Scholar
• Bhowmik, B. B.; Ganguly, P. Spectrochim. Acta A 2005, 61, 1997–2003.
   PubMed Web of Science ®Google Scholar
• Knight, C. G.; Stephens, T. Biochem. J. 1989, 258, 683–687.
   PubMed Web of Science ®Google Scholar
• (a) Wu, L.; Wu, Y.; Yan, F.; Fang, L. Monatsh. Chem. 2010, 141, 871–875; (b) Li, J.; Lu, L.; Su, W. Tetrahedron Lett. 2010, 51, 2434–2437; (c) Yadav, S.; Nand, B.; Khurana, J. M. Can. J. Chem. 2013, 91, 698–703; (d) Fatma, S.; Singh, P. K.; Ankit, P.; Shireen, M.; Singh, J. Tetrahedron Lett. 2013, 54, 6732–6736 (e) Amoozadeh, A.; Rahmani, S. J. Mol. Catal. A: Chem. 2015, 396, 96–107; (f) Moosavi-Zare, A. R.; Zolfigol, M. A.; Zarei, Zare, M.; Khakyzadeh, A. V. J. Mol. Liquids 2015, 211, 373–380; (g) Maleki, B.; Akbarzadeh, E.; Babaee, S. Dyes Pigm. 2015, 123, 222–234; (h) Habibi, D.; Kaamyabi, S.; Hazarkhani, H. Chin. J. Catal. 2015, 36, 362–366; (i) Singh, H.; Kumari, S.; Khurana, J. M. Chin. Chem. Lett. 2014, 25, 1336–1340; (j) Kour, M.; Paul, S.; Clark, J. H.; Gupta, V. K.; Kant, R. J. Mol. Catal. A: Chem. 2016, 411, 299–310.
   Web of Science ®Google Scholar
• Kuo, S. C.; Huang, L. J.; Nakamura, H. J. Med. Chem. 1984, 27, 539–544.
   PubMed Web of Science ®Google Scholar
• Radi, M.; Schenone, S.; Botta, M. Org. Biomol. Chem. 2009, 7, 2841–2847.
   PubMed Web of Science ®Google Scholar
• Banzatti, C.; Branzoli, U.; Lovisolo, P. P.; Melloni, P.; Salvadori, P. Arzneim Forsch 1984, 34, 864–869.
   PubMed Web of Science ®Google Scholar
• Nawwar, G. A.; Abdelrazek, F. M.; Swellam, R. H. Arch. Pharm. 1991, 324, 875–877.
   PubMed Web of Science ®Google Scholar
• Regnier, G. L.; Canevari, R. J.; Le Douarec, J. C.; Holstorp, S.; Daussy, J. J. Med. Chem. 1972, 15, 295–301.
   PubMed Web of Science ®Google Scholar
• Pershin, G. N.; Shcherbakova, L. I.; Zykova, T. N.; Sokolova, V. N. Farmakol Toksikol 1972, 35, 466–471.
   PubMedGoogle Scholar
• Mohr, S. J.; Chirigos, M. A.; Fuhrman, F. S.; Pryor, J. W. Cancer Res. 1975, 35, 3750–3754.
   PubMed Web of Science ®Google Scholar
• Bedair, A. H.; El-Hady, N. A.; El-Latif, M. S. A.; Fakery, A. H.; El-Agrody, A. M. Farmaco 2000, 55, 708–714.
   PubMedGoogle Scholar
• Heckler, R. E.; Jourdan, G. P. European Patent EP 414386, 1991.
   Google Scholar
• Bedair, A. H.; Emam, H. A.; El-Hady, N. A. Ahmed, K. A. R.; El-Agrody, A. M. Farmaco 2001, 56, 965–973.
   PubMedGoogle Scholar
• Nandi, G. C.; Samai, S.; Kumar, R.; Singh, M. S. Tetrahedron 2009, 65, 7129–7134.
   Web of Science ®Google Scholar
• Kumar, K. P.; Satyanarayana, S.; Lakshmi Reddy, P.; Nara-simhulu, G.; Ravirala, N.; Subba Reddy, B. V. Tetrahedron Lett. 2012, 53, 1738–1741.
   Web of Science ®Google Scholar
• Mohaqeq, M.; Safaei-Ghomi, J. Monatsh. Chem. 2015, 146, 1581–1586.
   Web of Science ®Google Scholar
• Kefayati, H.; Golshekan, M.; Shariati, S.; Ba, M. Chin. J. Catal. 2015, 36, 572–575.
   Web of Science ®Google Scholar
• Jalde, S. S.; Chavan, H. V.; Adsul, L. K.; Dhakane, V. D.; Bandgar, B. P. Synth. React. Inorg. Met. Org. Chem. 2014, 44, 623–626.
   Web of Science ®Google Scholar
• Azimi, S. C. Iranian J. Catal. 2015, 5, 41–48.
   Web of Science ®Google Scholar
• Khurana, J. M.; Lumb, A.; Chaudhary, A.; Nand, B. RSC Adv. 2013, 3, 1844–1854.
   Web of Science ®Google Scholar
• Sajadikhah, S. S. RSC Adv. 2015, 5, 28038–28043.
   Web of Science ®Google Scholar
• Maleki, B.; Barzegar, S.; Sepehr, Z.; Kermanian, M. Tayebee, R. J. Iran Chem. Soc. 2012, 9, 757–765.
   Web of Science ®Google Scholar
• Maleki, B.; Akbarzadeh, E.; Babaee, S. Dyes Pigm. 2015, 123, 222–234.
   Web of Science ®Google Scholar
• Maleki, B.; Gholizadeh, M.; Sepehr, Z. Bull. Korean Chem. Soc. 2011, 32, 1697–1702.
   Web of Science ®Google Scholar
• (a) Olyaei, A.; Ghodrat Alidoust, M. Synth. Commun. 2015, 45, 95–104; (b) Sadeghpour, M.; Olyaei, A.; Lotfiyan, J.; Rajabi, F. Synth. Commun. 2015, 45, 1311–1320; (c) Olyaei, A.; Gesmati, F.; Sadeghpour, M.; Shams, B.; Alizadeh, M. Synth. Commun. 2012, 42, 1650–1660; (d) Olyaei, A.; Rahbarian, F.; Sadeghpour, M. Chem. Heterocycl. Compd. 2015, 51, 899–902; (e) Sadeghpour, M.; Olyaei, A.; Rezaei, M. J. Heterocycl. Chem. 2016, 53, 981–988.
   Web of Science ®Google Scholar