Quinoxaline-2,3(1H,4H)-dithione: Synthesis and reactions

References

• Mahesh, R.; Dhar, A. K.; Tara Sasank, T. V. N. V.; Thirunavukkarasu, S.; Devadoss, T. Chin. Chem. Lett. 2011, 22, 389–392. doi:10.1016/j.cclet.2010.11.002.
   Web of Science ®Google Scholar
• Ingle, R. G.; Marathe, R. P. Int. J. Pharm. Res. Allied Sci. 2012, 1, 46–51.
   Google Scholar
• Das, P. J.; Sarkar, S. Int. J. Chem. Res. 2011, 3, 56–60. doi:10.9735/0975-3699.3.2.56-60.
   Google Scholar
• Geethavan, M.; Reddy, J. R; Sathyanarayana, S. V. Int. J. Pharm. Technol. 2012, 4, 4700–4710.
   Google Scholar
• Mohammad, V. S.; Saeed, B. World Appl. Sci. J. 2013, 21, 394–401.
   Google Scholar
• Morales-Castellanos, J. J.; Ramírez-Hernández, K.; Gómez-Flores, N. S.; Rodas-Suárez, O. R.; Peralta-Cruz, J. Molecules. 2012, 17, 5164–5176. doi:10.3390/molecules17055164.
   PubMed Web of Science ®Google Scholar
• Mohammad, R. I.; Hassani, Z. ARKIVOC. 2008, 2008, 280–287. doi:10.3998/ark.5550190.0009.f24.
   Google Scholar
• Khaksar, S.; Rostamnezhad, F. Bull. Korean Chem. Soc. 2012, 33, 2581–2584. doi:10.5012/bkcs.2012.33.8.2581.
   Web of Science ®Google Scholar
• Singh, S.; Mishra, P.; Srivastava, M.; Singh, S. B.; Singh J.; Tiwari, K. P. Green Chem. Lett. Rev. 2012, 5, 587–593. doi:10.1080/17518253.2012.681706.
   Web of Science ®Google Scholar
• Neri, J. M.; Cavalcanti, L. N.; Araújo, R. M.; Menezes, F. G. Arab. J. Chem. 2017, in press. doi:10.1016/j.arabjc.2017.07.012.
   Google Scholar
• Sasse K.; Wegler, H. R.; Unterstenhöfer, G.; Grewe F. Angew. Chem. 1960, 72, 973–981. doi:10.1002/ange.19600722410.
   Web of Science ®Google Scholar
• Chesseman, G. W. H.; Cookson, R. F. The Chemistry of Heterocyclic Compounds: Condensed Pyrazine, vol. 35; John Wiley & Sons: New York, 1979.
   Google Scholar
• Deshpande, S. S.; Kumbhar, H. S.; Shankarling, G. S. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2017, 174, 154–163. doi:10.1016/j.saa.2016.10.045.
   PubMed Web of Science ®Google Scholar
• Baashen, M. A.; Abdel-Wahab, B. F.; El-Hiti, G. A. Heterocycles. 2016, 92, 1931–1952. doi:10.3987/REV-16-847.
   Web of Science ®Google Scholar
• Baashen, M. A.; Abdel-Wahab, B. F.; El-Hiti G. A. Chem. Pap. 2017, 71, 2159–2166. doi:10.1007/s11696-017-0209-5.
   Web of Science ®Google Scholar
• Bagley, M. C.; Baashen, M.; Paddock, V. L.; Kipling, D.; Davis, T. Tetrahedron. 2013, 69, 8429–8438. doi:10.1016/j.tet.2013.07.055.
   Web of Science ®Google Scholar
• Bagley, M. C.; Baashen, M.; Dwyer, J.; Milbeo, P.; Kipling, D.; Davis, T. Future Medicine, London: UK, Chapter 5, 2014; pp. 86–104.
   Google Scholar
• Bagley, M. C.; Baashen, M.; Chuckowree, I; Dwyer, J.; Kipling, D.; Davis, T. Pharmaceuticals. 2015, 8, 257–276. doi:10.3390/ph8020257.
   Google Scholar
• Podsiadly, R.; Sokolowska, J. Dyes Pigm. 2012, 92, 1300–1307. doi:10.1016/j.dyepig.2011.09.006.
   Web of Science ®Google Scholar
• Taeger, E.; El-Hewehi, Z. J. Prakt. Chem. 1962, 18, 255–261. doi:10.1002/prac.19620180503.
   Google Scholar
• Beldi, R.; Atta, K. F.; Aboul-Ela, S.; El Ashry, E. S. H. J. Heterocycl. Chem. 2010, 48, 50–56. doi:10.1002/jhet.496.
   Web of Science ®Google Scholar
• Voloshin, Y. Z.; Belov, A. S.; Lebedev, A. Y.; Varzatskii, O. A.; Antipin, M. Y.; Starikova, Z. A.; Kron, T. E. Russ. Chem. Bull. 2004, 53, 1218–1222. doi:10.1023/B:RUCB.0000042276.31796.ca.
   Web of Science ®Google Scholar
• Shaikh, M.; Mohanty, J.; Singh, P. K.; Bhasikuttan, A. C.; Rajule, R. N.; Satam, V. S.; Bendre, S. R.; Kanetkar, V. R.; Pal, H. J. Phys. Chem. A. 2010, 114, 4507–4519. doi:10.1021/jp9107969.
   PubMed Web of Science ®Google Scholar
• Sonawane, Y. A.; Rajule, R. N.; Shankarling, G. S. Monatsh. Chem. 2010, 141, 1145–1151. doi:10.1007/s00706-010-0365-6.
   Web of Science ®Google Scholar
• Abdel-Ghany, H. Phosphorus Sulfur Silicon Relat. Elem. 2000, 164, 259–268. doi:10.1080/10426500008045251.
   Web of Science ®Google Scholar
• Pettersson, B.; Hasimbegovic, V.; Svensson, P. H.; Bergman, W. O. 2012104415A1 PCT/EP 051864, 2012.
   Google Scholar
• Boyde, S.; Garner, C. D.; Enemark, J. H.; Ortega, R. B. Polyhedron 1986, 5, 377–379. doi:10.1016/S0277-5387(00)84936-0.
   Web of Science ®Google Scholar
• Pilipenko, A. T.; Savranskii, L. I.; Ryabushko, O. P.; Krivokhizhina, L. A. Dopov. Akad. Nauk Ukr. RSR Ser. B. 1974, 36, 447–451.
   Google Scholar
• Yaroshenko, T. I.; Elokhina, V. N.; Nakhmanovich, A. S.; Larina, L. I.; Komarova, T. N.; Amosova, S. V. Russ. J. Gen. Chem. 2009, 79, 1197–1200. doi:10.1134/S1070363209060280.
   Web of Science ®Google Scholar
• Anacona, J. R.; Martell, T.; Sanchez, I. J. Chilean Chem. Soc. 2005, 50, 375–378.
   Web of Science ®Google Scholar
• Holzberger, A.; Holdt, H.-J.; Kleinpeter, E. Org. Biomol. Chem. 2004, 2, 1691–1697. doi:10.1039/B402224F.
   PubMed Web of Science ®Google Scholar
• Andriyankova, L. V.; Zhiveťev, S. A.; Maľkina, A. G.; Andriyankov, M. A.; Afonin, A. V.; Trofimov, B. A. Chem. Heterocycl. Compd. 2002, 38, 974–980. doi:10.1023/A:1020929832027.
   Google Scholar
• Elokhina, V. N.; Nakhmanovich, A. S.; Karnaukhova, R. V.; Kalikhman, I. D.; Bannikova, O. B. Chem. Heterocycl. Compd 1984, 20, 862–865.
   Google Scholar
• Nakhmanovich, A. S.; Elokhina, V. N.; Karnaukhova, R. V.; Skvortsova, G. G.; Kalikhman, I. D. Chem. Heterocycl. Compd. 1982, 18, 1154–1156.
   Google Scholar
• Smith, K.; Lindsay, C. M.; Matthews, I.; Wahlam, W.; Musmar, M. J.; Martin, G. E.; Hoffschwelle, A. F.; Lynch, V. M.; Simonsen, S. H. Sulfur Lett. 1992, 15, 69–89.
   Google Scholar
• Wolmershaeuser, G.; Kraft, G. Chem. Ber. 1989, 122, 385–387. doi:10.1002/cber.19891220230.
   Google Scholar
• Rastenyte, L.; Kupetis, G. K.; Eicher-Lorka, O.; Matijoska, A. Chemija. 1997, 75–78.
   Google Scholar