참고문헌
- Togni, A.; Grutzmacher, H. Catalytic Heterofunctionalization; Wiley-VCH: Verlag, GmbH, 2001.
- Likhar, P. R.; Roy, S.; Roy, M.; Subhas, M. S.; Kantam, M. L.; De, R. L. Synlett 2007, 2301.
- Heravi, M. M.; Bakhtiari, K.; Oskooie, H. A.; Taheri, S. J. Mol. Catal. A-Chem. 2007, 263, 279. https://doi.org/10.1016/j.molcata.2006.08.070
- Nandurkar, N. S.; Bhanushali, M. J.; Bhor, M. D.; Bhanage, B. M. J. Mol. Catal. A-Chem. 2007, 271, 14. https://doi.org/10.1016/j.molcata.2007.02.021
- Nanjundaswamy, H. M.; Pasha, M. A. Synth. Commun. 2006, 36, 3161. https://doi.org/10.1080/00397910600908835
- Ganguly, N. C.; Barik, S. K. Synthesis 2008, 425.
- Kabalka, G. W.; Pace, R. D.; Wadgankar, P. P. Synth. Commun. 1990, 20, 2453. https://doi.org/10.1080/00397919008053193
- Barton, D. H. R.; Beaton, J. M.; Geller, L. E.; Pechell, M. M. J. Am. Chem. 1961, 83, 4076. https://doi.org/10.1021/ja01480a030
- Sakamoto, T.; Kikugawa, Y. Synthesis 1993, 563.
- Kumar, H. M. S.; Mohanty, P. K.; Kumar, M. S.; Yadav, J. S. Synth. Commun. 1997, 27, 1327. https://doi.org/10.1080/00397919708006061
- Kabalka, G. W.; Pace, R. D.; Wadgaonkar, P. P. Synth. Commun. 1990, 20, 2453. https://doi.org/10.1080/00397919008053193
- Zolfigol, M. A.; Khazaei, A.; Ghorbani-Choghamarani, A.; Rostami, A. Phospourus, Sulfur 2006, 181, 2453. https://doi.org/10.1080/10426500600737435
- Kazaei, A.; Manesh, A. A. Synthesis 2004, 1739.
- Shirini, F.; Zolfigol, M. A.; Mallakpour, B.; Mallakpour, S. E.; Hajipour, A. R.; Mohammadpou-Baltork, I. Tetrahedron Lett. 2002, 43, 1555. https://doi.org/10.1016/S0040-4039(02)00007-2
- Ezabadi, A.; Najafi, G. R.; Hashemi, M. M. Chin. Chem. Lett. 2007, 18, 1451. https://doi.org/10.1016/j.cclet.2007.09.003
- Bhar, S.; Guha, S. Synth. Commun. 2005, 35, 1183. https://doi.org/10.1081/SCC-200054761
- Lakouraj, M. M.; Noorian, M.; Mokhtary, M. React. Funct. Polym. 2006, 66, 910. https://doi.org/10.1016/j.reactfunctpolym.2005.12.002
- Hashemi, M. M.; Rahimi, A.; Ahmadibeni, Y. Acta Chim. Slov. 2004, 51, 333.
- Karami, B.; Montazerozohori, M. Molecules 2006, 11, 720. https://doi.org/10.3390/11090720
- Telvekar, V. N. Synth. Commun. 2005, 35, 2827. https://doi.org/10.1080/00397910500290599
- Khazaei, A.; Manesh, A. A.; Rostami, A. Phosphorus, Sulfur 2004, 179, 2483. https://doi.org/10.1080/10426500490485471
- Murugan, R.; Reddy, B. S. R. Chem. Lett. 2004, 33, 1038. https://doi.org/10.1246/cl.2004.1038
- Li, D.; Shi, F.; Guo, S.; Deng, Y. Tetrahedron Lett. 2004, 45, 265. https://doi.org/10.1016/j.tetlet.2003.10.175
- Zolfigol, M. A.; Amani, K.; Ghorbani-Choghamarani, A.; Hajjami, M.; Ayazi-Nasrabadi, R.; Jafari, S. Catal. Commun. 2008, 9, 1739. https://doi.org/10.1016/j.catcom.2008.01.029
- Zolfigol, M. A.; Amani, K.; Hajjami, M.; Ghorbani-Choghamarani, A. Monatsh. Chem. 2008, 139, 895. https://doi.org/10.1007/s00706-008-0868-6
- Zolfigol, M. A.; Shirini, F.; Ghorbani-Choghamarani, A. Synthesis 2006, 2043.
- Zolfigol, M. A.; Bagherzadeh, M.; Mallakpour, S.; Chehardoli, G.; Kolvari, E.; Ghorbani-Choghamarani, A.; Koukabi, N. Catal. Commun. 2007, 8, 256. https://doi.org/10.1016/j.catcom.2006.04.006
- Zolfigol, M. A.; Bagherzadeh, M.; Mallakpour, S.; Chehardoli, G.; Ghorbani-Choghamarani, A.; Koukabi, N.; Dehghanian, M.; Doroudgar, M. J. Mol. Catal. A-Chem. 2007, 270, 219. https://doi.org/10.1016/j.molcata.2007.02.003
- Zolfigol, M. A.; Amani, K.; Ghorbani-Choghamarani, A.; Hajjami, M. Monatsh. Chem. 2008, (In press).
피인용 문헌
- An Efficient and New Method on the Oxidative Coupling of Thiols under Mild and Heterogeneous Conditions vol.30, pp.6, 2008, https://doi.org/10.5012/bkcs.2009.30.6.1388
- Chemoselective and Catalytic Trimethylsilylation of Alcohols and Phenols by 1,1,1,3,3,3-Hexamethyldisilazane and Catalytic Amounts of PhMe3N+Br3- vol.31, pp.9, 2008, https://doi.org/10.1016/s1872-2067(10)60107-6
- Hypervalent iodine(iii)-mediated oxidation of aldoximes to N-acetoxy or N-hydroxy amides vol.8, pp.2, 2008, https://doi.org/10.1039/b917096k
- Green and Metal-free Catalytic Oxidation of Urazoles into Triazolinediones by Guanidinium Nitrate and Catalytic Amounts of Silica Sulfuric Acid vol.31, pp.8, 2008, https://doi.org/10.5012/bkcs.2010.31.8.2389
- Rapid and Efficient Method for Room Temperature Deoximation Reaction Under Solvent-Free Conditions vol.32, pp.7, 2008, https://doi.org/10.5012/bkcs.2011.32.7.2482
- Mononitration of phenol derivatives by guanidinium nitrate and silica sulfuric acid under mild conditions vol.22, pp.12, 2011, https://doi.org/10.1016/j.cclet.2011.07.012
- Ultrasound-assisted facile one-pot sequential synthesis of novel sulfonamide-isoxazoles using cerium (IV) ammonium nitrate (CAN) as an efficient oxidant in aqueous medium vol.40, pp.1, 2008, https://doi.org/10.1016/j.ultsonch.2017.07.019
- Iron‐Enabled Utilization of Air as the Terminal Oxidant Leading to Aerobic Oxidative Deoximation by Organoselenium Catalysis vol.361, pp.3, 2019, https://doi.org/10.1002/adsc.201801163
- AIBN‐Initiated Oxidative Deoximation Reaction: A Metal‐Free and Environmentally‐Friendly Protocol vol.10, pp.3, 2008, https://doi.org/10.1002/ajoc.202000675
- Selenium-catalyzed selective reactions of carbonyl derivatives: state-of-the-art and future challenges vol.23, pp.13, 2008, https://doi.org/10.1039/d1gc00961c