تعداد نشریات | 418 |
تعداد شمارهها | 9,997 |
تعداد مقالات | 83,560 |
تعداد مشاهده مقاله | 77,801,198 |
تعداد دریافت فایل اصل مقاله | 54,843,855 |
Silica sulfuric acid: an efficient catalyst for the synthesis of substituted indazoles | ||
Journal of the Iranian Chemical Research | ||
مقاله 6، دوره 3، شماره 3، اسفند 2010، صفحه 191-194 اصل مقاله (98.37 K) | ||
نویسندگان | ||
Digambar D. Gaikwad* 1؛ Rajendra P. Pawar2 | ||
1Department of Chemistry, Govt.College of Arts & Sciences, Aurangabad-4310001, India | ||
2Department of Chemistry, Deogiri College, Aurangabad- 431005, India | ||
چکیده | ||
A simple extremely fast and efficient approach for the synthesis of substituted indazole in good to excellent yield catalyzed by using silica sulfuric acid (SSA) in DMSO solvent at room temperature. This is solid state reaction have been attracting the synthetic organic chemist as they provided enhance reaction rates, less environmental pollution, greater selectivity, cleaner products and manipulative simplicity. Various indazoles are obtained in moderate to excellent yield. | ||
کلیدواژهها | ||
Ortho-hydroxy aromatic aldehydes/ketones؛ Hydrazine hydrate؛ Silica sulphuric acid | ||
مراجع | ||
[1] J. Elguero, A. Fruchier, E.M. Tjiou, S. Trofimenko, Chem. Heterocyclic Comoud. 31 (1995) 1006- 1010. [2] Z. Zhong, T. Xu, X. Chen, Y. Qui, Z. Zhang, J. Chem. Soc Perkin Trans. I, 1 (1993) 1279-1280. [3] M.R.G. Da-Costa, M.J.M. Curto, S.G. Davies, M.T. Duarte, C. Resende, F.C. Teixeira, J. Organometallic Chem. 604 (2000) 157-169. [4] S.Z. Süleyman, A. Rüstem, Synthetic Comm. 32 (2002) 3399-23411. [5] I. Kiyofumi, K. Mika, Y. Takashi, S. Ikue, H. Kou, S. Takao, Chem. Letts. 33 (2004) 1026-1027. [6] H. Yoshiyuk, S. Yoshimichl, A. Toyohiko, Synthesis 8 (2004) 1183-1186. [7] L.J. Barry, D.R. James, Synthetic Comm. 35 (2005) 2681-2684. [8] N. Miklos, V. Andrea, Z. Weimin, W.G. Paul. B. Gabor, T. Laszlo, Tetrahedron 60 (2004) 9937-9944. [9] Y.L. Artyom, S.K. Anton, Z.V. Alexander, J. Org. Chem. 70 (2005) 596-602. [10] L. Kirill, C.H. Margaret, F.M. Dilinie, L. Robert, J. Org. Chem. 71 (2006) 8166-8172. [11] I. Kiyofumi, K. Mika, Y. Takashi, A. Yukari, H. Kou, S. Takao, Tetrahedron 63 (2007) 2695-2711. [12] J.S. Yadav, B.V.S. Reddy, K. Sadasive, G. Satheesh, G. Tetrahedron Lett. 43 (2002) 9695-9697. [13] L. Bouissane, S.E. Kazzouli, J.M. Leger, C. Jarry, E.M. Rakib, M. Khouili, G. Guillaumet, Tetrahedron Lett. 61 (2005) 8218-8225. [14] C.T. Fatima, R. Helene, F.A. Ines, M. Joao, M. Curto, D.M. Teresa, Molecules 11 (2006) 867-871. [15] D.J. Varughese, M.S. Manhas, A.K. Bose, Tetrahedron Lett. 47 (2006) 6795-6798. [16] C.I. Dellerba, M. Novi, G. Petrillo, C. Tsavani, Tetrahedron 50 (1994) 3529-3530. [17] A.Y. Lebedev, A.S. Khahrtulyari, A.Z. Voskoboynikov, J. Org. Chem. 37 (2005) 257-263. [18] P.D. Lokhande, A. Raheem, S.T. Sabale, A.R. Chabukswar, S.C. Jagdale, Tetrahedron Lett. 48 (2007) 6890-6892. [19] M. Cheung, A. Boloor, J. A. Stafford, J. Org. Chem. 68 (2003) 4093-4095. [20] P. Salehi, M.A. Zolfigol, F. Shirini M. Baghbanzadeh, Curr. Org Chem. 10 (2006) 2171-2189. [21] D. Gaikwad, A. Syed, R. Pawar, Chem. Tech. 1 (2008) 442-445. | ||
آمار تعداد مشاهده مقاله: 539 تعداد دریافت فایل اصل مقاله: 443 |