DOI QR코드

DOI QR Code

Chemistry of 1-Methoxypyrrole-2-carboxylic Acid

  • 발행 : 1989.12.20

초록

1-Methoxypyrrole-2-carboxylic acid and its derivatives were prepared. Fridel-Crafts bromination occurs first at 4-position and then at 5-position. Acylation of 3-methyl derivative was also directed to 4-position.

키워드

참고문헌

  1. The Chemistry of Pyrroles R. A. Jones;G. P. Bean
  2. Ann. Chem. v.236 L. Knorr
  3. J. Org. Chem. v.53 F. W. Keana;G. S. Heo;J. S. Mann;F. L. Van Nice;L. Lex;V. S. Prabhu;G. Ferguson
  4. J. Org. Chem. v.19 E. C. Kornfeld;R. G. Jones
  5. J. Am. Chem. Soc. v.56 A. H. Blatt
  6. J. Am. Chem. Soc. v.58 A. H. Blatt
  7. Ann. Chim. (Italy) v.49 V. Sprio;G. C. Vaccaro
  8. Ann. Chim. (Italy) v.50 V. Sprio;P. Madonia
  9. Ann. Chim. (Italy) v.50 V. Sprio;I. Fabra
  10. Bull. Soc. Chim. France R. Ramasseul;A. Rassat
  11. Izvest. Akad. Nauk S.S.S.R., Ser. khim. E. G. Rozantsev;A. A. Medzhidov;M. B. Neiman
  12. Bull. Soc. Chim. France G. Rio;A. Ranjon;O. Pouchot
  13. J. Org. Chem. v.37 E. E. Schweizer;C. M. Kopay
  14. J. Am. Chem. Soc. v.98 R. A. Abramovitch;B. W. Cue, Jr.
  15. Ann. Chem. v.236 L. Knorr
  16. Atti Accad. Lincei v.94 A. Angeli;G. Marchetti
  17. Ger. Offen. 1,917,048 R. Ramasseul;A. Rassat
  18. C. R. Acad. Sci. Ser. C v.158 E. E. Blaise
  19. Bull. Soc. Chim. France R. Ramasseul;A. Rassat;G. Rio;M. J. Scholl
  20. Z. Naturforsch., Tell B v.31 no.B R. Kreher;H. Pawelczyk
  21. J. Org. Chem. v.38 R. A. Abramovitch;B. W. Cue, Jr.
  22. The Chemistry of Pyrroles R. A. Jones;G. P. Bean
  23. Tetrahedron Lett. v.22 J. Rokach;P. Hamel;M. Kakushima;G. M. Smith
  24. J. Med. Chem. v.16 D. M. Bailey;R. E. Johnson
  25. Ger. 1,137,434 H. Geipel
  26. Chem. Abstracts v.58 H. Geipel

피인용 문헌

  1. ChemInform Abstract: Chemistry of 1‐Methoxypyrrole‐2‐carboxylic Acid. vol.21, pp.22, 1990, https://doi.org/10.1002/chin.199022137
  2. Discovery, characterization and functional improvement of kumamonamide as a novel plant growth inhibitor that disturbs plant microtubules vol.11, pp.1, 1989, https://doi.org/10.1038/s41598-021-85501-1