References
- Williams, D. L. H. Supplement F2: The Chemistry of Amino, Nitroso, Nitro and Related Groups; John Wiley & Sons Ltd.: 1996; pp 665-682.
- Keefer, L. K.; Williams, D. L. H. Methodsin Nitric Oxide Reseach; John Wiley & Sons Ltd.: 1996; pp 509-519.
- Furniss, B. S.; Hannaford, A. J.; Smith, P. W. G.; Tatchell, A.R. Vogels Text Book of Practical Organic Chemistry, 4th Ed.;Longman: London and New York, 1986.
- Sheriner, R. L.; Reynold, T. L.; Fuson, C.; Curtin, D. Y.; Morrill, T. C. TheSystematic Identification of Organic Compounds, 6th Ed.; JohnWiley and Sons: 1980; pp 220-223.
- Castedo, L.; Riguera, R.; Vezquez, M. P. J. Chem. Soc. Chem. Commun. 1983, 301.
- Fanning, J. C.; Keefer, L. K.; Larry, K. J. Chem. Soc. Chem.Commun. 1987, 955.
- Nakajima, M.; Warner, J. C.; Anselme, J. P. Tetrahedron Lett.1984, 25, 2619. https://doi.org/10.1016/S0040-4039(01)81245-4
- Chang, S. K.; Hrrington, G. W.; Rothstein, M.; Shergalis, W. A.;Swern, D.; Vohra, S. K. Cancer Res. 1979, 39, 3871.
- Makhova, N. N.; Karpov, G. A.; Mikhailyuk, A. N.; Bova, A. E.;Khmel´nitskii, L. I.; Novikov, S. S. Izv. Akad. Nauk. SSSR. Ser.Khim. 1978, 1, 226.
- Zolfigol, M. A. Synth. Commun. 1999, 29, 905. https://doi.org/10.1080/00397919908086051
- Zolfigol, M. A.; Ghaemi, E.; Madrakian, E.; Kiany-Borazjani, M. Synth.Commun. 2000, 30, 2057. https://doi.org/10.1080/00397910008087255
- Zolfigol, M. A.; Shirini, F.; Ghorbani Choghamarani, A.; Taqian-Nasab, A.; Keypour, H.;Salehzadeh, S. J. Chem. Research(S) 2000, 420
- Zolfigol, M. A.; Nematollahi, D.; Mallakpour, S. E. Synth. Commun. 1999, 29, 2277. https://doi.org/10.1080/00397919908086229
- Zolfigol, M. A.; Mallakpour, S. E.; Synth. Commun. 1999, 29, 4061. https://doi.org/10.1080/00397919908085927
- Zolfigol, M. A.; Kiany- Borazjani, M.; Sadeghi, M. M.; Mohammadpoor-Baltork, I.; Memarian, H. R. Synth. Commun. 2000, 30, 551. https://doi.org/10.1080/00397910008087352
- Zolfigol, M. A. Synth. Commun. 2000, 30, 1593. https://doi.org/10.1080/00397910008087194
- Zolfigol, M. A.; Ghaemi, E.; Madrakian, E. Synth. Commun. 2000, 30, 1689. https://doi.org/10.1080/00397910008087210
- Zolfigol, M. A.; Mallakpour, S. E.; Madrakian, E.; Ghaemi, E. Indian J. Chem. 2000, 39B, 308.
- Zolfigol, M. A.; Kiany-Borazjani, M.; Sadeghi, M. M.; Memarian, H. R.; Mohammadpoor-Baltork, I. J. Chem. Research(S) 2000, 167.
- Zolfigol, M. A.; Kiany- Borazjani, M.; Sadeghi, M. M.; Memarian, H. R.; Mohammadpoor- Baltork, I. Synth. Commun. 2000, 30, 2945. https://doi.org/10.1080/00397910008087444
- Zolfigol, M. A.; Kiany-Borazjani, M.; Mallakpour, S. E.; Nassr-Isfahani, H. Synth. Commun. 2000, 30, 2573. https://doi.org/10.1080/00397910008087422
- Zolfigol, M. A.; Kiany-Borazjani, M.; Sadeghi, M. M.; Mohammadpoor-Baltork, I.; Memarian, H. R. Synth. Commun. 2000, 30, 3919. https://doi.org/10.1080/00397910008086949
- Barton, S. D.; Ollis, W. D. Comprehensive Organic Chemistry;Pergamon Press: 1968; Vol. 2, pp 363-370.
- Turnbull, K. J. Heterocycl. Chem. 1985, 22, 965. https://doi.org/10.1002/jhet.5570220406
- Keypour, H.; Pritchard, R. G.; Parish, R. V. Transition Met.Chem. 1998, 23, 609. https://doi.org/10.1023/A:1006988704602
- Keypour, H.; Pritchard, R. G.; Parish, R. V. Transition Met. Chem. 1998, 23, 121. https://doi.org/10.1023/A:1006982723501
- Keypour, H.; Salehzadeh, S. Transition Met. Chem. 2000, 25, 205. https://doi.org/10.1023/A:1007017400893
- Keypour, H.; Salehzadeh, S.; Pritchard, R. G.; Parish, R. V. Inorg. Chem. 2000, 39, 5787. https://doi.org/10.1021/ic000511m
- Ellison, M. K.; Schulz, C. E.; Scheidt, W. R. Inorg. Chem. 2000,39, 5102. https://doi.org/10.1021/ic000789e
- Richter-Addo, G. B. Acc. Chem. Res. 1999, 32, 529. https://doi.org/10.1021/ar970351r
Cited by
- A Green Approach to the Synthesis of 2,3-Dihydropyrimidin-2(1H)-ones by Uronium Hydrogensulfate under Solvent-free Conditions vol.65, pp.5, 2005, https://doi.org/10.3987/COM-04-10312
- Uronium Hydrogen Sulfate/Urea-Hydrogen Peroxide as a Green and Metal-Free Catalytic System for the Efficient, Chemo-, and Homoselective Oxidation of Sulfides to Sulfoxides vol.186, pp.2, 2011, https://doi.org/10.1080/10426507.2010.494919
- Al(HSO4)3: an efficient and heterogeneous reusable catalyst for the synthesis of 1-amidoalkyl-2-naphthols under thermal solvent-free conditions vol.9, pp.1, 2012, https://doi.org/10.1007/s13738-011-0009-8
- as an Efficient Procedure for the Chemoselective N-Nitrosation of Secondary Amines vol.53, pp.3, 2013, https://doi.org/10.1002/jccs.200600088
- Metal Hydrogen Sulfates Catalyzed Methoxymethylation of Alcohols under Solvent-Free Conditions vol.54, pp.4, 2013, https://doi.org/10.1002/jccs.200700153
- -Nitrosation of Secondary Amines Using Supported Perchloric Acid on Silica Gel and Stereoselectivity Study of Nitrosated Products pp.00094536, 2013, https://doi.org/10.1002/jccs.201300136
- Chemoselective synthesis of 1,1-diacetates from aldehydes in the presence of Al(HSO4)3 under mild solvent-free conditions vol.43, pp.6, 2007, https://doi.org/10.1134/S1070428007060085
- 1,3,5-Triazine-2,4,6-triyltrisulfamic acid (TTSA): A new organic solid acid for the nitrosation of secondary amines and oxidation of urazoles in the presence of NaNO2 under mild and heterogeneous conditions vol.121, pp.4, 2009, https://doi.org/10.1007/s12039-009-0052-5
- Chemoselective N-Nitrosation of Secondary Amines under Mild and Heterogeneous Conditions. vol.34, pp.43, 2003, https://doi.org/10.1002/chin.200343053
- An Efficient Procedure for Deprotection of Acetals under Mild and Heterogeneous Conditions vol.25, pp.7, 2003, https://doi.org/10.5012/bkcs.2004.25.7.1075
- Solvent-Free Preparation of 1,1-Diacetates from Aldehydes Mediated by Zirconium Hydrogen Sulfate at Room Temperature vol.53, pp.4, 2003, https://doi.org/10.1002/jccs.200600127
- Chemoselective N-nitrosation of secondary amines under heterogeneous and mild conditions via in situ generation of HNO2 vol.20, pp.4, 2003, https://doi.org/10.1016/j.cclet.2008.12.044