DOI QR코드

DOI QR Code

Bromodecarboxylation of Arylpropiolic Acids with Oxone and Sodium Bromide.


초록

키워드

참고문헌

  1. Houben-Weyl Methoden der Organishen Chemie. v.5 no.2a Jager, V.Muller.(Ed.)
  2. Preparative Actetylenic Chemistry. Brandsma, L.(Ed.)
  3. J. Org. Chem. v.51 Boutin, R. H.;Rapoport, H.
  4. Synth. Commun. v.15 no.463 Norin, T.;Unelius, R.
  5. Angew. Chem. Int. v.23 Hofmeister, H.;Annen, K.;Laurent, H.;Wiechert, R.
  6. J. Org. Chem. v.59 Shair, M. D.;Yoon, T.;Danishefsky, J. S.
  7. J. Chem. Soc. Chem. Commun. Lee, J.;Shim, J.
  8. Macromolecules. v.26 Kwock, E. W.;Bird, T. Jr.;Miller, T. M.
  9. Chem. Phys. Lett. v.214 no.333 Polzonetti, G.;Russo, M. V.;Furlani, A.;infante, G.
  10. J. Chem. Soc. Chem. Commun. v.1424 Fouquery, C.;Lehn, J. M.;Malthete, J.
  11. J. Chem. Soc. Chem. Commun. v.14 no.909 Jeffry, T.
  12. Synth. Commun. v.25 no.2295 Rao, M. L. N.;Periasamy, M.
  13. J. Am. Chem. Soc. v.115 no.2528 Ochiai, M.;Uemura, K.;Masaki, Y.
  14. J. Tetrahedron Lett. v.35 no.4777 Ratovelomanana, V.;Rollin, Y.;Gebehenne, C.;Gosmini, C.;Perichon.
  15. J. Tetrahedron Lett. v.35 no.3529 Grandjean, D.;Pale, P.;Chuche, J.
  16. J. Tetrahedron Lett. v.40 no.8549 Michel, P.;Gennet, D.;Rassat, A.
  17. J. Org. Chem. v.51 no.4354 Li, P.;Alper, H.
  18. Tetrahedron Lett. v.31 no.3141 Wanger, A.;Heitz, M. P.;Mioskowski, C.
  19. Tetrahedron Lett. v.36 no.2619 Brunel, Y.;Roussea, G.
  20. Tetrahedron Lett. v.40 no.1495 Hosmi, F.;Rousseau, G.
  21. Ann. v.446 no.49 Wieland, H.;Fischer, F. G.
  22. J. Am. Chem. Soc. v.100 no.1525 Ehrlich, S. J.;Berliner, E.
  23. J. Org. Chem. v.49 no.515 Cohen, M. J.;McNelis, E.
  24. J. Org. Chem. v.64 no.6896 Naskar, D.;Roy, S.
  25. Tetrahedron Lett. v.40 no.1495 Hosmi, F.;Rousseau, G.
  26. Synlett. v.105 You, H. W.;Lee, K. J.
  27. J. Org. Chem. v.25 no.1901 Kennedy, R. J.;Stock, A. M.
  28. J. Am. Chem. Soc. v.106 no.2462 Jeyaraman, R. J.;Murray, R. W.
  29. J. Tetrahedron Lett. v.29 no.4501 Zabrowski, D. L.;Moormann, A. E.;Beck, K. R.
  30. J. Org. Chem. v.53 no.2087 Davis, F. A.;Chattopadhyay, S.;Towson, J. C.;Lai, S.;Reddy, T.
  31. Synlett. v.235 Greenhalgh, R. P.
  32. J. Org. Chem. v.60 no.8412 Cecchereli, P.;Curini, M.;Epifano, F.;Marcotullio, M. C.;Rosati, O.
  33. Synlett. v.1059 Paradkar, V. M.;Lathan, T. B.;Demko, D. M.;
  34. Synlett. v.777 Curini, M.;Epifano, F.;Marcotullio, M. C.;Rosati, O.
  35. Synlett. v.767 Ceccherelli, P.;Curi, M.;Marcotullio, M. C.;Epifano, F.;Rosati, O.
  36. Synth, Commun. v.27 no.3835 Subhas Bose, D.;Srinivas, P.
  37. Synth. Commun. v.28 no.3057 Ceccherelli, P.;Curini, M.;Epofano, F.;Marcotullio, M. C.;Rosati, O.
  38. Tetrahedron Lett. v.37 no.2377 Dieter, R. K.;Nice, L. E.;Velu, S. E.
  39. J. Tetrahedron Lett. v.38 no.2805 Ross, S. A.;Burrows, C.
  40. J. Am. Chem. Soc. v.77 no.5549 Newman, M. S.;Merrill, S. H.
  41. J. Am. Chem. Soc. v.96 no.7820 Montgomery, R. E.
  42. Chem. Ber. v.75 no.291 Hunsdiecker, H. C.
  43. In Comprehensive Organic Synthesis. v.7 Crich, D.;Trost, B. M.;Steven, V. L.(Eds.)
  44. Org. React. v.19 no.326 Sheldon, R. A.;Kochi, J. K.
  45. J. Org. Chem. v.26 no.280 Cristol, S. J.;Firth, W. C. Jr.

피인용 문헌

  1. Bromination of Activated Arenes by Oxone® and Sodium Bromide vol.23, pp.5, 2001, https://doi.org/10.5012/bkcs.2002.23.5.773
  2. Decarboxylative Tribromination for the Selective Synthesis of Tribromomethyl Ketone and Tribromovinyl Derivatives vol.360, pp.20, 2001, https://doi.org/10.1002/adsc.201800851