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Synthesis of 2-Substituted-1,3-Oxazole-4-Carboxaldehyde via 1,3-Dipolar Cycloaddition

  • Hong-Seok Kim (Department of Industrial Chemistry, Kyungpook National University) ;
  • Sang Hwa Kim (Department of Industrial Chemistry, Kyungpook National University) ;
  • Hak Ki Lee (Department of Industrial Chemistry, Kyungpook National University)
  • 발행 : 1993.08.20

초록

키워드

참고문헌

  1. J. Am. Chem. Soc. v.108 Y. Kato;N. Fusetani;S. Matsunaga;K. Hashimoto;S. Fujita;T. Furuya
  2. J. Org. Chem. v.53 Y. Kato;N. Fusetani;S. Matsunaga;K. Hashimoto;K. Koseki
  3. Tetrahedron v.47 S. Matsunaga;S. Fujita;H. Sakata;N. Fusetani
  4. J. Antibiotics v.37 S. Iwasaki;H. Kobayashi;J. Furukawa;S. Okuda;Z. Sato;I. Matsuda;T. Noda
  5. J. Antibiotics v.39 S. Iwasaki;M. Namikoshi;H. Kobayashi;J. Furukawa;S. Okuda;A. Itai;A. Kasuya;Y. Iitaka;Z. Sato
  6. J. Am. Chem. Soc. v.113 T. Ichiba;W. Y. Yoshida;P. J. Scheuer;T. Higa;D. G. Gravalos
  7. J. Am. Chem. Soc. v.113 N. Fusetani;T. Sugawara;S. Matunaga
  8. J. Am. Chem. Soc. v.113 J. Kobayashi;F. Itagaki;H. Shigemori;M. Ishiashi;K. Takahashi;M. Ogura;S. Nagasawa;T. Nakamura;H. Hirota;T. Ohata;S. Nozoe
  9. Chem. Lett. v.431 H. Tada;T. Tozyo;Y. Terui;F. Hayashi
  10. oxazoles I. J. Turchi(ed.)
  11. Chem. Rew. v.75 I. J. Turchi;J. S. Dewar
  12. Chem. Rew. v.86 H. H. Wasserman;K. E. McCarthy;K. S. Prowse
  13. Nat. Prod. Rep. v.9 J. R. Lewis
  14. J. Org. Chem. v.51 A. I. Meyer;J. P. Lawson;D. G. Walker;R. J. Linderman
  15. Tetrahedron Lett. v.32 Z. Zhao;G. R. Scaarlato;R. W. Armstrong
  16. Synlett. F. Yokokawa;Y. Hamada;T. Shiori
  17. Synlett. F. Yokokawa;Y. Hamada;T. Shiori
  18. Synlett. F. Yokokawa;Y. Hamada;T. Shiori
  19. Synlett. D. W. Knight;G. Pattenden;D. E. Rippon
  20. J. Org. Chem. v.57 R. F. Cunico;C. P. Kuan
  21. Tetrahedron Lett. v.32 R. D. Connell;M. Tebbe;P. Helquist;B. Akermark
  22. Tetrahedron Lett. v.27 R. D. Connell;F. Scavo;B. Akermark;P. Helquist
  23. Tetrahedron Lett. v.33 S.-K. Yoo
  24. J. Org. Chem. v.55 E. Wenkert;T. P. Ananthanarayan;V. F. Ferreira;M. G. Hoffman;H.-S. Kim
  25. Bull. Korean Chem. Soc. H.-S. Kim;Y. H. Yoon
  26. Tetrahedron Lett. v.32 R. D. Connell;M. Tebbe;P. Helquist;B. Akermark
  27. Collect. Czech. Chem. Commun. v.38 Z. Arnold;J. Sauliova;V. Krchnak
  28. Collect. Czech. Chem. Commun. v.38 Z. Arnold;J. Sauliova
  29. J. Org. Chem. v.57 D. L. Boger;T. T. Curran

피인용 문헌

  1. Diazoaldehyde Chemistry. Part 1. Transdiazotization of Acylacetaldehydes in Neutral-to-Acidic Medium. A Direct Approach to the Synthesis of α-Diazo-β-oxoaldehydes vol.77, pp.8, 1993, https://doi.org/10.1002/hlca.19940770819
  2. ChemInform Abstract: Synthesis of 2-Substituted 1,3-Oxazole-4-carboxaldehyde via 1,3- Dipolar Cycloaddition. vol.25, pp.13, 1993, https://doi.org/10.1002/chin.199413173
  3. Synthesis of 2-Substituted-4-carbethoxythiazoles vol.32, pp.3, 1993, https://doi.org/10.1002/jhet.5570320344
  4. Large-Scale Preparation of 2-Methyloxazole-4-carboxaldehyde vol.12, pp.1, 2008, https://doi.org/10.1021/op700198s
  5. Thermal Rearrangement of Azido Ketones into Oxazoles via Azirines: One‐Pot, Metal‐Free Heteroannulation to Functionalized 1,3‐Oxazoles vol.2013, pp.2, 1993, https://doi.org/10.1002/ejoc.201201269
  6. Chemoselectivity in the Reaction of 2‐Diazo‐3‐oxo‐3‐phenylpropanal with Aldehydes and Ketones vol.96, pp.9, 1993, https://doi.org/10.1002/hlca.201200532