${\alpha}$,N-Diphenylnitrone 유도체에 대한 Cysteine 및 Thiophenol의 친핵성 첨가물에 관한 연구

Synthetic Studies on the Nucleophilic Addition of Cysteine and Thiophenol to ${\alpha}$,N-Diphenylnitrone Derivatives

  • Tae-Rin Kim (Department of Chemistry, Korea University) ;
  • Sang-Yong Pyun (Department of Chemistry, Korea University) ;
  • Man-So Han (Department of Chemistry, Korea University) ;
  • Kwang-Il Lee (Department of Chemistry, Kyungki University)
  • 발행 : 1991.06.20

초록

${\alpha}$,N-diphenylnitrone에 cysteine과 thiophenol을 반응시켜 4개의 thiazolidine과 다음의 5가지 새로운 화합물을 합성하였다. ${\alpha}$,thiophenoxy-benzylidene aniline : ${\alpha}$, thiophenoxy-p-hydroxybenzylidene aniline : ${\alpha}$,thiophenoxy-p-chlorobenzylidene aniline : ${\alpha}$,thiophenoxy-p-methoxybenzylidene aniline : ${\alpha}$,thiophenoxy-p-nitrobenzylidene aniline. 이 화합물들의 구조는 원소분석, UV-, IR 및 NMR- 스펙트럼에 의해 확인하였다.

Four thiazolidines and following five new compounds were prepared by the addition reaction of cysteine and thiophenol to ${\alpha}$,N-diphenylnitrones, respectively ; ${\alpha}$,thiophenoxy-benzylidene aniline ;${\alpha}$,thiophenoxy-p-hydroxybenzylidene aniline ; ${\alpha}$,thiophenoxy-p-chlorobenzylidene aniline ;${\alpha}$,thiophenoxy-p-methoxybenzylidene aniline ; ${\alpha}$,thiophenoxy-p-nitrobenzylidene aniline. The structure of these compounds were confirmed by the elemental analysis, UV-, IR-and NMR-spectra.

키워드

참고문헌

  1. Modern Synthetic Reaction H. O. House
  2. Orgnic Reaction v.10 E. D. Bergman
  3. Advanced Organic Chemistry E. A. Royals
  4. J. Am. Chem. Soc. v.106 C. F. Bernasconi;K. A. Haward;A. Kanavarioti
  5. J. Am. Chem. Soc. v.111 C. F. Bernasconi;P. Paschalis
  6. J. Org. Chem. v.54 C. F. Bernasconi;R. B. Killon
  7. J. Am. Chem. Soc. v.110 C. F. Bernasconi;R. D. Bunnell;F. Tenier
  8. J. Org. Chem. v.53 C. F. Bernasconi;D. A. Kliner;A. S. Mullin
  9. The Chemistry of the Carbon-Nitrogen double bond S. Sandrfy
  10. Nature v.223 R. A. Alarcon;J. Meinhofer
  11. J. Med. Chem. v.15 K. Y. Zee-Cheng;C. C. Cheng
  12. J. Chem. Soc., Perkin Trans, I v.15 M. Masui;K. Suda;M. Yamauchi
  13. Tetrahedron v.32 H. Esterbauer;A. Ertl;N. Scholz
  14. J. Kor. Chem. Soc. v.7 T. R. Kim;S. J. Yun;B. B. Park
  15. Angew. Chem. Intern. v.2 R. Huisgen
  16. Bull. Chem. Soc., Japan v.33 S. Kimura
  17. Org. Syn., Coll. v.1 O. Kamm
  18. J. Am. Chem. Soc. v.78 O. H. Wheeler;D. H. Gore