References
- Williams, D. L. H. Nitrosation; Cambridge University Press: Cambridge, 1988; pp 77-149
- Williams, D. L. H.; Supplement F2: The Chemistry of Amino, Nitroso, Nitro and Related Groups; John Wiley & Sons Ltd.: New York, 1996; pp 665-682
- Keefer, L. K.; Williams, D. L. H. Methods in Nitric Oxide Research; John Wiley & Sons Ltd.: New York, 1996; p 509
- Nudelman, N. S.; Bonatti, A. E. Synlett 2000, 1825
- Olszewska, T.; Milewska, M. J.; Gdaniec, M.; Matuszynska, H.; Potonski, T. J. Org. Chem. 2001, 66, 501 https://doi.org/10.1021/jo001311v
- Castedo, L.; Riguera, R.; Vezquez, M. P. J. Chem. Soc., Chem. Commun. 1983, 301
- Nakajima, M.; Warner, J. C.; Anselme, J. P. Tetrahedron Lett. 1984, 25, 2619 https://doi.org/10.1016/S0040-4039(01)81245-4
- Makhova, N. N.; Karpov, G. A.; Mikhailyuk, A. N.; Bova, A. E.; Khamel_nitskii, I.; Novikov, S. S. Izv. Akad. Nauk. SSSR, Ser. Khim. 1978, 1, 226
- Chang, S. K.; Harrington, G. W.; Rothstein, M.; Shergalis, W. A.; Swern, D.; Vohra, S. K. Cancer Res. 1979, 39, 3871
- Zolfigol, M. A. Synth. Commun. 1999, 29, 905 https://doi.org/10.1080/00397919908086051
- Zolfigol, M. A.; Habibi, D.; Mirjalili, B. F.; Bamoniri, A. Tetrahedron Lett. 2003, 44, 3345 https://doi.org/10.1016/S0040-4039(03)00578-1
- Zolfigol, M. A.; Ghorbani-Choghamarani, A.; Hazarkhani, H. Synlett 2002, 1002
- Zolfigol, M. A. Tetrahedron 2001, 57, 9509 https://doi.org/10.1016/S0040-4020(01)00960-7
- Olah, G. A.; Molhotra, R.; Narang, S. C. J. Org. Chem. 1987, 43, 4628
- Zolfigol, M. A.; Shirin, F.; Ghorbani Choghamarani, A.; Mohammadpoor-Baltork, I. Green Chem. 2002, 4, 562 https://doi.org/10.1039/b208328k
- Zolfigol, M. A.; Bamoniri, A. Synlett 2002, 1621
- Mirjalili, B. F.; Zolfigol, M. A.; Bamoniri, A. J. Korean Chem. Soc. 2001, 45, 546
- Mirjalili, B. F.; Zolfigol, M. A.; Bamoniri, A. Molecules 2002, 7, 751 https://doi.org/10.3390/71000751
- Mirjalili, B. F.; Zolfigol, M. A.; Bamoniri, A.; Zarei, A. Bull. Korean Chem. Soc. 2003, 24, 400 https://doi.org/10.5012/bkcs.2003.24.3.400
- Mirjalili, B. F.; Zolfigol, M. A.; Bamoniri, A.; Zaghaghi, Z. J. Chem. Research(S) 2003, 273
- Mirjalili, B. F.; Zolfigol, M. A.; Bamoniri, A.; Zaghaghi, Z.; Hazar, A. Acta Chem. Slov. 2003, 50, 563
- Shirini, F.; Zolfigol, M. A.; Mohammadi, K. Bull. Korean Chem. Soc. 2004, 25, 325 https://doi.org/10.5012/bkcs.2004.25.2.325
- Harmer, M. A.; Sun, Q. Appl. Catal. A: General 2001, 221, 45 https://doi.org/10.1016/S0926-860X(01)00794-3
- Heydari, A.; Larijani, H.; Emami, J.; Karami, B. Tetrahedron Lett. 2000, 41, 2471 https://doi.org/10.1016/S0040-4039(00)00182-9
- Asgarian Damavandi, J.; Zolfigol, M. A.; Karami, B. Synth. Commun. 2001, 31, 129
Cited by
- Synthesis of Aza-Polycyclic Compounds: Novel Phenazines and Quinoxalines using Molybdate Sulfuric Acid (MSA) vol.31, pp.2, 2011, https://doi.org/10.1080/10406638.2011.572577
- One-Pot Synthesis of Dihydropyrimidine-Thione Derivatives Using Tungstate Sulfuric Acid (TSA) as a Recyclable Catalyst vol.187, pp.6, 2012, https://doi.org/10.1080/10426507.2011.616562
- A Modified Synthesis of Some Novel Polycyclic Aromatic Phenazines and Quinoxalines by Using the Tungstate Sulfuric Acid (TSA) as a Reusable Catalyst under Solvent-free Conditions vol.59, pp.2, 2012, https://doi.org/10.1002/jccs.201100421
- Facile and Rapid Synthesis of 9-Aryl 1,8-dioxoöctahydroxanthenes Derivatives using Tungstate Sulfuric Acid vol.45, pp.3, 2013, https://doi.org/10.1080/00304948.2013.764790
- Molybdate Sulfuric Acid/NaNO2: A Novel Heterogeneous System for theN-Nitrosation of Secondary Amines under Mild Conditions vol.89, pp.12, 2006, https://doi.org/10.1002/hlca.200690261
- Silica-supported ICl as a novel heterogeneous system for the rapid oxidation of urazoles to triazolinediones vol.19, pp.4, 2008, https://doi.org/10.1002/hc.20444
- )-ones catalyzed by tungstate sulfuric acid in solvent-free conditions vol.45, pp.4, 2008, https://doi.org/10.1002/jhet.5570450438
- Tungstate Sulfuric Acid (TSA)/NaNO2 as a Novel Heterogeneous System for the N-Nitrosation of Secondary Amines under Mild Conditions. vol.36, pp.47, 2005, https://doi.org/10.1002/chin.200547045
- Chemoselective N-nitrosation of secondary amines under heterogeneous and mild conditions via in situ generation of HNO2 vol.20, pp.4, 2005, https://doi.org/10.1016/j.cclet.2008.12.044
- N-Nitrosation of Secondary Amines Using p-TSA-NaNO2 as a Novel Nitrosating Agent Under Mild Conditions vol.40, pp.5, 2005, https://doi.org/10.1080/00397910903009448
- Novel Tri- and Tetra-substituted Pyrimido[4,5-d]pyridazines: Regiospecific Synthesis Catalyzed by Silica Supported Yttrium Trinitrate vol.34, pp.12, 2005, https://doi.org/10.5012/bkcs.2013.34.12.3677