DOI QR코드

DOI QR Code

Debromination of α-Bromoketones and vic-Dibromides Using a NaI/Na2SO3 System

  • Lee, Seung-Hwan (Graduate School of Biotechnology, Korea University) ;
  • Chang, Yu-Mi (Graduate School of Biotechnology, Korea University) ;
  • Yoon, Cheol-Min (Department of New Material Chemistry, Korea University)
  • Published : 2004.11.20

Abstract

Keywords

References

  1. Alonso, F.; Beletskaya, I. P.; Yus, M. Chem. Rev. 2002, 102, 4009. https://doi.org/10.1021/cr0102967
  2. Gemal, A. L.; Luche, J. L. Tetrahedron lett. 1980, 21, 3195. https://doi.org/10.1016/S0040-4039(00)77443-0
  3. Olah, G. A.; Arvanaghi, M.; Vankar, Y. D. J. Org. Chem. 1980, 45, 3531. https://doi.org/10.1021/jo01305a040
  4. Rosenkranz, G.; Mancera, O.; Gatica, J.; Djerassi, C. J. Am. Chem. Soc. 1950, 72, 1658.
  5. Olah, G. A.; Vankar, Y. D.; Fung, A. P. Synthesis 1979, 59.
  6. Solo, A. J.; Singh, B. J. Org. Chem. 1965, 30, 1658. https://doi.org/10.1021/jo01016a511
  7. Butcher, T. S.; Detty, M. R. J. Org. Chem. 1999, 64, 5677. https://doi.org/10.1021/jo990332q
  8. Ono, A.; Fujimoto, E.; Ueno, M. Synthesis 1986, 570.
  9. Choi, H. Y.; Chi, D. Y. Org. Lett. 2003, 5, 411. https://doi.org/10.1021/ol0271638
  10. Choi, H. Y.; Chi, D. Y. J. Am. Chem. Soc. 2001, 123, 9202. https://doi.org/10.1021/ja0164374
  11. Butcher, T. S.; Detty, M. R. J. Org. Chem. 1998, 63, 177. https://doi.org/10.1021/jo971504r
  12. Kim, I.-K.; Jung, O. J. Bull. Korean Chem. Soc. 2002, 23(7), 990. https://doi.org/10.5012/bkcs.2002.23.7.990
  13. Holder, A. A.; Marshall, S. C.; Wang, P. G.; Kwak, C.-H. Bull. Korean Chem. Soc. 2003, 24(3), 350. https://doi.org/10.1007/s11814-007-5045-9
  14. Encyclopedia of Reagents for Organic Synthesis; Paquette, L. A., Ed.; JOHN WILEY & SONS Ltd: 1995; Vol. 7, p 4587
  15. Townsend, J. M.; Spenser, T. A. Tetrahedron Lett. 1971, 137.
  16. Encyclopedia of Reagents for Organic Synthesis; Paquette, L. A., Ed.; JOHN WILEY & SONS Ltd: 1995; Vol. 7, p 4648

Cited by

  1. Lewis Basicity of Water for a Selective Monodehalogenation of α,α-Dihalo Ketones to α-Halo Ketones and Mechanistic Study vol.360, pp.2, 2017, https://doi.org/10.1002/adsc.201701233
  2. Debromination of ?-Bromoketones and vic-Dibromides Using a NaI/Na2SO3 System. vol.36, pp.14, 2005, https://doi.org/10.1002/chin.200514051
  3. An improved and sustainable approach for the synthesis of α,β-dibromo ketones using ceric ammonium nitrate and ammonium bromide vol.5, pp.1, 2016, https://doi.org/10.1515/gps-2015-0097
  4. Synthetic Utilization of α,β‐Chalcone Dibromide In Heterocyclic Chemistry and Stereoselective Debromination vol.4, pp.39, 2004, https://doi.org/10.1002/slct.201902262
  5. Synthesis of novel heterocycles using 1,2,3‐triazole‐4‐carbohydrazides as precursors vol.57, pp.3, 2004, https://doi.org/10.1002/jhet.3840