References
- Andersson, P. G.; Munslow, I. J. Modern Reduction Methods; Wiley-VCH: New York, 2008.
- Burke, S. D.; Danheiser, R. L. Handbook of Reagents for Organic Synthesis, Oxidizing and Reducing Agents; Wiley-VCH: New York, 1999.
- Seyden- Penne, J. Reductions by the Alumino and Borohydrides in Organic Synthesis; 2nd ed., Wiley-VCH: New York, 1997.
- Abdel- Magid, A. F. Reductions in Organic Synthesis; ACS Symposium Seies, 1996. Vol. 641.
- Hudlicky, M. Reductions in Organic Chemistry; Ellis Horwood: Chichester, 1984.
- Abdel-Magid, A. F.; Carson, K. G.; Harris, B. D.; Maryanoff, C. A.; Shah, R. D. J. Org. Chem. 1996, 61, 3849. https://doi.org/10.1021/jo960057x
- Nutaitis, C. F.; Bernardo, J. E. J. Org. Chem. 1989, 54, 5629. https://doi.org/10.1021/jo00284a046
- Narayana, C.; Periasamy, M. Tetrahedron Lett. 1985, 26, 1757. https://doi.org/10.1016/S0040-4039(00)98331-X
- Hutchins, R. O.; Learn, K.; El-Telbany, F.; Stercho, Y. P. J. Org. Chem. 1984, 49, 2438. https://doi.org/10.1021/jo00187a028
- Brown, H. C.; Kim, S. C.; Krishnamurthy, S. J. Org. Chem. 1980, 45, 1. https://doi.org/10.1021/jo01289a001
- Lane, C. F. Synthesis 1975, 135.
- Lalancette, J. M.; Freche, A.; Brindle, J. R.; Laliberte, M. Synthesis 1972, 526.
- Narasimhan, S.; Balakumar, R. Synth. Commun. 2000, 30, 4387. https://doi.org/10.1080/00397910008087061
- Narasimhan, S.; Balakumar, R. Aldrichimica Acta 1998, 31, 19.
- Ravi Kumar, K. S.; Baskaran, S.; Chandrasekaran, S. Tetrahedron Lett. 1993, 34, 171. https://doi.org/10.1016/S0040-4039(00)60086-2
- Fujii, H.; Oshima, K.; Utimoto, K. Chem. Lett. 1991, 20, 1847.
- Soai, K.; Ookawa, A. J. Org. Chem. 1986, 51, 4000. https://doi.org/10.1021/jo00371a017
- Marks, T. J.; Kolb, J. R. Chem. Rev. 1977, 77, 263. https://doi.org/10.1021/cr60306a004
- Firouzabadi, H.; Adibi, M.; Zeynizadeh, B. Synth. Commun. 1998, 28, 1257. https://doi.org/10.1080/00397919808005968
- Firouzabadi, H.; Adibi, M. Phosphorus, Sulfur, Silicon Relat. Elem. 1998, 142, 125. https://doi.org/10.1080/10426509808029672
- Firouzabadi, H.; Adibi, M. Synth. Commun. 1996, 26, 2429. https://doi.org/10.1080/00397919608004555
- Firouzabadi, H.; Afsharifar, G. R. Bull. Chem. Soc. Jpn. 1995, 68, 2595. https://doi.org/10.1246/bcsj.68.2595
- Pasumansky, L.; Goralski, C. T.; Singaram, B. Org. Proc. Res. Dev. 2006, 10, 959. https://doi.org/10.1021/op0600759
- Cainelli, G.; Giacomini, D.; Panunzioa, M.; Martelli, G.; Spunta, G. Tetrahedron 1985, 41, 1385. https://doi.org/10.1016/S0040-4020(01)96540-8
- Blough, B. E.; Carroll, F. I. Tetrahedron Lett. 1993, 34, 7239. https://doi.org/10.1016/S0040-4039(00)79297-5
- Zeynizadeh, B.; Setamdideh, D. Asian J. Chem. 2009, 21, 3603.
- Zeynizadeh, B.; Setamdideh, D.; Faraji, F. Bull. Korean Chem. Soc. 2008, 29, 76. https://doi.org/10.5012/bkcs.2008.29.1.076
- Zeynizadeh, B. Bull. Chem. Soc. Jpn. 2003, 76, 317. https://doi.org/10.1246/bcsj.76.317
- Zeynizadeh, B.; Faraji, F. Bull. Korean Chem. Soc. 2003, 24, 453. https://doi.org/10.5012/bkcs.2003.24.4.453
- Zeynizadeh, B.; Zahmatkesh, K. J. Chin. Chem. Soc. 2004, 51, 801.
- Fleet, G. W. J.; Harding, P. J. C. Tetrahedron Lett. 1981, 22, 675. https://doi.org/10.1016/S0040-4039(01)92520-1
- Zeynizadeh, B.; Setamdideh, D. Asian J. Chem. 2009, 21, 3588.
- Haghgooie, H.; Zeynizadeh, B.; Shafaghi, M. Asian J. Chem. 2008, 20, 6033.
- Zeynizadeh, B.; Behyar, T. J. Braz. Chem. Soc. 2005, 16, 1200. https://doi.org/10.1590/S0103-50532005000700018
- Zeynizadeh, B.; Behyar, T. Bull. Chem. Soc. Jpn. 2005, 78, 307. https://doi.org/10.1246/bcsj.78.307
- Zeynizadeh, B.; Yahyaei, S. Bull. Korean Chem. Soc. 2003, 24, 1664. https://doi.org/10.5012/bkcs.2003.24.11.1664
- Zeynizadeh, B.; Shirini, F. Bull. Korean Chem. Soc. 2003, 24, 295. https://doi.org/10.5012/bkcs.2003.24.3.295
- Zeynizadeh, B.; Shirini, F. J. Chem. Res. 2003, 335.
- Ganem, B.; Osby, J. O. Chem. Rev. 1986, 86, 763. https://doi.org/10.1021/cr00075a003
- Lakouraj, M. M.; Tajbakhsh, M.; Mahalli, M. S. Monatsh. Chem. 2008, 139, 117. https://doi.org/10.1007/s00706-007-0756-5
- Tamami, B.; Lakoraj, M. M.; Yeganeh, H. Iranian Poly. J. 1997, 6, 159.
- Liu, W.-Y.; Xu, Q.-H.; Ma, Y.- X. Org. Prep. Proced. Int. 2000, 32, 596. https://doi.org/10.1080/00304940009355960
- Sim, T. B.; Ahn, J. H.; Yoon, N. M. Synthesis 1996, 324.
- Yakabe, S.; Hirano, M.; Morimoto, T. Synth. Commun. 1999, 29, 295. https://doi.org/10.1080/00397919908085770
- Yoon, N. M.; Choi, J. Synlett 1993, 135.
- Firouzabadi, H.; Tamami, B.; Goudarzian, N. Synth. Commun. 1991, 21, 2275. https://doi.org/10.1080/00397919108021586
- Bram, G.; d'Incan, E.; Loupy, A. J. Chem. Soc. Chem. Commun. 1981, 1066.
- Larock, R. C. Comprehensive Organic Transformations, A Guide to Functional Group Preparations; 2nd ed., Wiley-VCH: Weinheim, 2010.
- Rao, H. S. P.; Bharathi, B. Indian J. Chem. 2002, 41B, 1072.
- Kano, S.; Tanaka, Y.; Sugino, E.; Hibino, S. Synthesis 1980, 695.
- Spreitzer, H.; Buchbauer, G.; Püringer, C. Tetrahedron 1989, 45, 6999. https://doi.org/10.1016/S0040-4020(01)89166-3
- Itsuno, S.; Sakurai, Y.; Ito, K. Synthesis 1988, 995.
- Bell, K. H. Aust. J. Chem. 1970, 23, 1415. https://doi.org/10.1071/CH9701415
- Gribble, G. W.; Nutaitis, C. F. Org. Prep. Proced. Int. 1985, 17, 317. https://doi.org/10.1080/00304948509355522
- Gribble, G. W.; Leiby, R. W.; Sheehan, M. N. Synthesis 1977, 856.
- Hutchins, R. O.; Natale, N. R. Org. Prep. Proced. Int. 1979, 11, 201. https://doi.org/10.1080/00304947909354852
- Borch, R. F.; Bernstein, M. D.; Durst, H. D. J. Am. Chem. Soc. 1971, 93, 2897. https://doi.org/10.1021/ja00741a013
- Hutchins, R. O.; Learn, K.; Nazer, B.; Pytlewski, D.; Pelter, A. Org. Prep. Proced. Int. 1984, 16, 335. https://doi.org/10.1080/00304948409457891
- Leeds, J. P.; Kirst, H. A. Synth. Commun. 1988, 18, 777. https://doi.org/10.1080/00397918808057845
- Cho, B. T.; Seong, S. Y. Bull. Korean Chem. Soc. 1988, 9, 322.
- Bandgar, B. P.; Nikat, S. M.; Wadgaonkar, P. P. Synth. Commun. 1995, 25, 863. https://doi.org/10.1080/00397919508013422
- Zeynizadeh, B.; Zahmatkesh, K. J. Chin. Chem. Soc. 2005, 52, 109.
- Dunn, P. J.; Wells, A. S.; Williams, M. T. Green Chemistry in the Pharmaceutical Industry; Wiley-VCH: Weinheim, 2010.
- Sheldon, R. A.; Arends, I.; Hanefeld, U. Green Chemistry and Catalysis; Wiley-VCH: Weinheim, 2007.
- Doble, M.; Kumar, A. Green Chemistry and Engineering; Elsevier: New York, 2007.
- Doxsee, K.; Hutchison, J. Green Organic Chemistry: Strategies, Tools, and Laboratory Experiments; Brooks/Cole: Belmont, CA, 2004.
- Tanaka, K. Solvent-free Organic Synthesis; 2nd ed., Wiley-VCH: Weinheim, 2009.
- Itsuno, S.; Sakurai, Y.; Shimizu, K.; Ito, K. J. Chem. Soc., Perkin Trans. 1 1990, 1859.
- Itsuno, S.; Sakurai, Y.; Shimizu, K.; Ito, K. J. Chem. Soc., Perkin Trans. 1 1989, 1548.
- Zeynizadeh, B.; Amjadi, E. Asian J. Chem. 2009, 21, 3611
Cited by
- System. vol.43, pp.9, 2012, https://doi.org/10.1002/chin.201209037
- The efficient solvent-free reduction of oximes to amines with NaBH3CN catalyzed by ZrCl4/nano Fe3O4 system vol.12, pp.5, 2015, https://doi.org/10.1007/s13738-014-0550-3
- Rapid and green reduction of aromatic/aliphatic nitro compounds to amines with NaBH4 and additive Ni2B in H2O vol.12, pp.7, 2015, https://doi.org/10.1007/s13738-014-0585-5
- A review on green Lewis acids: zirconium(IV) oxydichloride octahydrate (ZrOCl2·8H2O) and zirconium(IV) tetrachloride (ZrCl4) in organic chemistry vol.42, pp.5, 2016, https://doi.org/10.1007/s11164-015-2260-6
- Magnetic Fe3O4 nanoparticles as recovery catalyst for preparation of oximes under solvent-free condition vol.3, pp.1, 2013, https://doi.org/10.1186/2193-8865-3-57
- An improved and practical synthesis of Fmoc Rink linker vol.43, pp.3, 2011, https://doi.org/10.1177/1747519819836490
- Heterogeneous palladium-based catalyst promoted reduction of oximes to amines: using H2 at 1 atm in H2O under mild conditions vol.4, pp.6, 2011, https://doi.org/10.1039/c9re00003h