Bulletin of the Korean Chemical Society

  • 제24권5호
  • /
  • Pages.653-654
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  • 2003
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Reduction of Nitro Group Using Indium-wire in Water

  • Cho, Yong-Seo (Biochemicals Research Center, Korea Institute of Science and Technology) ;
  • Jun, Bo-Kyung (Biochemicals Research Center, Korea Institute of Science and Technology) ;
  • Kim, Sang-Hee (Biochemicals Research Center, Korea Institute of Science and Technology) ;
  • Cha, Joo-Hwan (Biochemicals Research Center, Korea Institute of Science and Technology) ;
  • Pae, Ae-Nim (Biochemicals Research Center, Korea Institute of Science and Technology) ;
  • Koh, Hun-Yeong (Biochemicals Research Center, Korea Institute of Science and Technology) ;
  • Chang, Moon-Ho (Biochemicals Research Center, Korea Institute of Science and Technology) ;
  • Han, So-Yeop (Department of Chemistry, Ewha Womans University)
  • 발행 : 2003.05.20
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참고문헌

  1. Hudlicky, M. Reductions in Organic Chemistry, 2nd Ed.; ACS Monograph, 1996.
  2. Scriven, E. F. V. Chemical Review 1988, 88, 297. https://doi.org/10.1021/cr00084a001
  3. Pae, A. N.; Cho, Y. S. Current Organic Chemistry 2002, 6, 715. https://doi.org/10.2174/1385272023374030
  4. Moody, C. J.; Pitts, M. R. Synlett 1988, 1028.
  5. Reddy, G. V.; Rao, G. V.; Iyengar, D. S. Tetrahedron Lett. 1999, 40, 3937. https://doi.org/10.1016/S0040-4039(99)00614-0
  6. Yadav, J. S.; Reddy, B. V. S.; Srinivas, R.; Ramalingam, T. Synlett 2000, 1447.
  7. Yadav, J. S.; Reddy, B. V. S.; Reddy, M. M. Tetrahedron Lett. 2000, 41, 2663. https://doi.org/10.1016/S0040-4039(00)00218-5
  8. Ranu, B. C.; Dutta, J.; Guchhait, S. K. J. Org. Chem. 2001, 66, 5624. https://doi.org/10.1021/jo010262z
  9. Ranu, B. C.; Samanta, S.; Guchhait, S. K. J. Org. Chem. 2001, 66, 4102. https://doi.org/10.1021/jo0102314
  10. Ranu, B. C.; Dutta, P.; Sarkar, A. J. Chem. Soc., Perkin Trans. 1 1999, 1139.
  11. Park, L.; Keum, G.; Kang, S. B.; Kim, K. S.; Kim, Y. J. Chem. Soc., Perkin Trans. 1 2000, 4462.
  12. Shin, J. A.; Choi, K. I.; Pae, A. N.; Koh, H. Y.; Kang, H.-Y.; Cho, Y. S. J. Chem. Soc., Perkin Trans. 1 2001, 946.
  13. Lee, J. G.; Choi, K. I.; Koh, H. Y.; Kim, Y.; Kang, Y.; Cho, Y. S.Synthesis 2001, 1, 81.

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  2. Recent developments in the reduction of aromatic and aliphatic nitro compounds to amines. pp.1520-586X, 2016, https://doi.org/10.1021/acs.oprd.6b00205
  3. Nanocrystalline Magnesium Oxide-Stabilized Palladium(0): An Efficient and Reusable Catalyst for Selective Reduction of Nitro Compounds vol.350, pp.6, 2008, https://doi.org/10.1002/adsc.200800018
  4. Synthesis of α-Ketobutyrolactones and γ-Hydroxy-α-Keto Acids vol.24, pp.12, 2003, https://doi.org/10.5012/bkcs.2003.24.12.1819
  5. Reduction of Nitro Group Using Indium-Wire in Water. vol.34, pp.45, 2003, https://doi.org/10.1002/chin.200345070
  6. Synthesis of Chromane Derivatives via Indium-mediated Intramolecular Allenylation and Allylation to Imines vol.25, pp.11, 2003, https://doi.org/10.5012/bkcs.2004.25.11.1627
  7. Selective Reduction of the Nitro-group Using Co2(CO)8-H2O vol.25, pp.11, 2004, https://doi.org/10.5012/bkcs.2004.25.11.1717
  8. Preparation of Chromane Derivatives via Indium-mediated Intramolecular Allylation Reactions vol.25, pp.8, 2003, https://doi.org/10.5012/bkcs.2004.25.8.1123
  9. Rapid, efficient and selective reduction of aromatic nitro compounds with sodium borohydride and Raney nickel vol.274, pp.1, 2003, https://doi.org/10.1016/j.molcata.2007.05.020
  10. Selective Reduction of Nitro Compounds Using CeY Zeolite Under Microwaves vol.54, pp.1, 2010, https://doi.org/10.5012/jkcs.2010.54.01.055
  11. A distinct novel approach for the synthesis of 3-indolyl-methanamines starting from indoles, aldehydes and nitrobenzenes in water vol.3, pp.34, 2003, https://doi.org/10.1039/c3ra41131a
  12. Polymethylhydrosiloxane derived palladium nanoparticles for chemo- and regioselective hydrogenation of aliphatic and aromatic nitro compounds in water vol.4, pp.43, 2003, https://doi.org/10.1039/c4ra01333f