Journal of the Korean Chemical Society (대한화학회지)

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

N-Benzoyl-4,4-dimethyl-2-methylamino-2-thiazoline as a Chemoselective Benzoylating Reagent

화학선택적인 Benzoylation 시약으로서 N-Benzoyl-4,4-dimethyl-2-methylamino-2-thiazoline

  • Yang, Garp-Yeol (Department of Applied Chemistry and The Research Institute for Catalysis, Chonnam National University) ;
  • Kim, Taek-Hyeon (Department of Applied Chemistry and The Research Institute for Catalysis, Chonnam National University)
  • 양갑열 (전남대학교 공과대학 응용화학공학부 및 촉매연구소) ;
  • 김택현 (전남대학교 공과대학 응용화학공학부 및 촉매연구소)
  • Published : 2003.12.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Greene, T. W.; Wuts, P. G. M. Protective group in Organic Synthesis; John Willey and Sons, Inc.: New York, 1991; p. 503.
  2. Itoh, M.; Hagiwara, D.; Kamiya, T. Bull. Chem. Soc. Jpn. 1977, 50, 718-721. https://doi.org/10.1246/bcsj.50.718
  3. Kita, Y.; Haruta, J.; Yasuda, H.; Fujunaga, K.; Shirouchi, Y.; Tamura, Y. J. Org. Chem. 1982,47,2697-2700. https://doi.org/10.1021/jo00135a003
  4. Nagao, Y.; Seno, K.; Kawabata. K.; Miyasaka, T.; Takao, S.; Fujita, E. Chem. Pharm. Bull. 1984, 32, 2687-2699. https://doi.org/10.1248/cpb.32.2687
  5. Sharma, S. K.; Miller, M. J.; Payne, S. M. J. Med. Chem. 1989, 32, 357-367. https://doi.org/10.1021/jm00122a013
  6. Kikugawa, Y.; Mitsui, K.; Sakamoto, T.; Kawase, M.; Tamiya, H. Tetrahedron Lett. 1990, 31, 243-246. https://doi.org/10.1016/S0040-4039(00)94382-X
  7. Katritzky, A. R.; Chang, H. X. Synthesis 1995, 62, 503-505.
  8. OSullivan, M. C.; Dalrymp1e, D. M.; Tetrahedron Lett. 1995, 36, 3451-3452. https://doi.org/10.1016/0040-4039(95)00630-U
  9. Xu, D.; Prasad, K.; Repic, O.; Blacklock, T. J.; Tetrahedron Lett. 1995, 36, 7357-7360. https://doi.org/10.1016/0040-4039(95)01655-4
  10. Atkinson, R. S.; Barker, E.; Sutcliffe, M. J. Chem. Commun. 1996, 1051-1052.
  11. Blagbrough, I. S.; Geall, A. J. Tetrahedron Lett. 1998, 39, 439-442. https://doi.org/10.1016/S0040-4039(97)10542-1
  12. Kondo, K.; Sekimoto, E.; Miki, K.; Murakami, Y. J. Chem. Soc., Perkin Trans. 1 1998, 2973-2974.
  13. Yasuhara, T.; Nagaoka, Y.; Tomioka, K. J. Chem. Soc., Perkin Trans. 1 1999, 2233-2234.
  14. Kondo, K.; Sekimoto, E.; Nakao, J.; Murakami, Y. Tetrahedron 2000, 56, 5843-5856. https://doi.org/10.1016/S0040-4020(00)00549-4
  15. Kim, T. H.; Cha, M. -H. Tetrahedron Lett. 1999, 40, 3125-3128. https://doi.org/10.1016/S0040-4039(99)00457-8
  16. Kim, T. H.; Yang, G. -Y. Tetrahedron Lett. 2002, 43, 9553-9557. https://doi.org/10.1016/S0040-4039(02)02414-0
  17. Kim, T. H.; Chun, J. C. Bull. Korean Chem. Soc. 2003, 24, 157-158. https://doi.org/10.5012/bkcs.2003.24.2.157
  18. Argay, G.; Kalman, A.; Toth, G.; Toldy, L. Tetrahedron Lett. 1972, 3179-3182.
  19. Mc. Arnett, E.; Miller, J. G.; Day, A. R. J. Am. Chem. Soc. 1950, 72, 5635-5638. https://doi.org/10.1021/ja01168a075
  20. Mc. Arnett, E.; Miller, J. G.; Day, A. R. J. Am Chem. Soc. 1951, 73, 5393-5395. https://doi.org/10.1021/ja01155a113