Bulletin of the Korean Chemical Society

  • 제23권1호
  • /
  • Pages.19-20
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  • 2002
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Investigation of the Cyclization of N-(2-Hydroxyethyl)-N'-phenylthioureas:Mitsunobu Conditions vs TsCl/NaOH System

  • Lee, Gue-Jae (Faculty of Applied Chemistry, Chonnam National University) ;
  • Kim, Jae-Nyoung (Department of Chemistry, Chonnam National University) ;
  • Kim, Taek-Hyeon (Faculty of Applied Chemistry, Chonnam National University)
  • 발행 : 2002.01.20
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참고문헌

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  2. Hughes, D. L. Org. React. 1992, 42, 335
  3. Comins, D. L.; Gao, J. Tetrahedron Lett. 1994, 35, 2819 https://doi.org/10.1016/S0040-4039(00)76633-0
  4. Walker, M. A. J. Org. Chem. 1995, 60, 5352 https://doi.org/10.1021/jo00121a070
  5. Edwards, M. L.; Stemerick, D. M.; McCarthy, J. R. Tetrahedron Lett. 1990, 31, 3417 https://doi.org/10.1016/S0040-4039(00)97411-2
  6. Fukuyama, T.; Jow, C. K.; Cheung, M. Tetrahedron Lett. 1995, 36, 6373 https://doi.org/10.1016/0040-4039(95)01316-A
  7. Fabiano, E.; Golding, B. T.; Sadeghi, M. M. Synthesis 1987, 190
  8. Roush, D. M.; Patel, M. M. Synth. Commun. 1985, 15, 675. https://doi.org/10.1080/00397918508063857
  9. Galeotti, N.; Montagne, C.; Poncet, J.; Jouin, P. Tetrahedron Lett. 1992, 33, 2807. https://doi.org/10.1016/S0040-4039(00)78864-2
  10. Wipf, P.; Miller, C. P. Tetrahedron Lett. 1992, 33, 6267. https://doi.org/10.1016/S0040-4039(00)60949-8
  11. Kim, T. H.; Lee, N.; Lee, G.-J.; Kim, J. N. Tetrahedron 2001, 57, 7137 https://doi.org/10.1016/S0040-4020(01)00682-2
  12. Mitsunobu, O.; Kato, K.; Kakese, F. Tetrahedron Lett. 1969, 2473.
  13. Mitsunobu, O.; Kato, K.; Tomari, M. Tetrahedron 1970, 26, 5731. https://doi.org/10.1016/0040-4020(70)80009-6
  14. Kim, T. H.; Min, J. K.; Lee, G.-J. Bull. Korean Chem. Soc. 2000, 21, 919
  15. Fell, J. B.; Coppola, G. M. Synth. Commun. 1995, 25, 43 https://doi.org/10.1080/00397919508010787
  16. Kim, T. H.; Lee, N.; Kim, J. N. Bull. Korean Chem. Soc. 2001, 22, 761

피인용 문헌

  1. ChemInform Abstract: Investigation of the Cyclization of N-(2-Hydroxyethyl)-N′-phenylthioureas: Mitsunobu Conditions vs TsCl/NaOH System. vol.33, pp.28, 2010, https://doi.org/10.1002/chin.200228057
  2. An efficient synthesis of [D6]leucocrystal violet vol.54, pp.4, 2010, https://doi.org/10.1002/jlcr.1849
  3. Novel Tandem Reaction for the Synthesis of N′-Substituted 2-Imino-1,3-oxazolidines from Vicinal (sec- or tert-)Amino Alcohol of Desosamine vol.2011, pp.13, 2011, https://doi.org/10.1002/ejoc.201001707
  4. 2-Phenylamino-2-oxazolines from N-(2-Hydroxyethyl)-N-phenylthioureas using TsCl/NaOH vol.47, pp.6, 2003, https://doi.org/10.5012/jkcs.2003.47.6.671
  5. A convenient method for the synthesis of 2-amino substituted aza-heterocycles from N,N'-disubstituted thioureas using TsCl/NaOH vol.60, pp.44, 2002, https://doi.org/10.1016/j.tet.2004.08.031
  6. N-Benzyloxycarbonyl-2-phenylaminooxazolidine as a Selective Amine Benzyloxycarbonylating Reagent vol.26, pp.6, 2002, https://doi.org/10.5012/bkcs.2005.26.6.983
  7. N-Acyl-2-phenyliminooxazolidines as Chemoselective Monoacylating Agents vol.26, pp.7, 2002, https://doi.org/10.5012/bkcs.2005.26.7.1027
  8. Double Asymmetric Alkylation Reactions Using C2-symmetric Benzene Based Bis(2-amino-2-oxazolines) Chiral Auxiliaries vol.32, pp.11, 2002, https://doi.org/10.5012/bkcs.2011.32.11.4133
  9. A Controlled Cyclization of Functionalized Thioureas and Unprecedented Termolecular Decyclization of Iminothiazolidinones vol.4, pp.12, 2002, https://doi.org/10.1002/slct.201900832