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Ruthenium-Catalyzed Reductive Heteroannulation of Nitroarenes with Trialkanolamines Leading to Indoles.


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References

  1. v.25 Remers, W. A.;Spande, T. F. Inoles.;Houlihan, W. J.(Ed.)
  2. Angew. Chem. Int. Ed. Engl. v.27 Hegedus, L. S.
  3. Heterocycles. no.27 Sakamoto, T.;Kondo, Y.;Yamanaka, H.
  4. J. In Comprehensive Heterocyclclic Chemistry Ⅱ. v.2 Sundberg, R. J.;Katritzky, A. R.;Rees, C. W.;Scriven, E. F. V.(Eds.)
  5. J. Indoles. Sunberg, R. J.
  6. J. Chem. Commun. Cho, C. S.;Lim, H. K.;Shim, S. C.;Kim, T. J.;Choi, H.
  7. Tetrahedron Lett. v.41 Cho, C. S.;Kim, J. H.;Shim, S. C.
  8. Tetrahedron. v.57 Cho, C. S.;Oh, B. H.;Shim, S. C.
  9. Tetrahedron Lett. v.40 Cho, C. S.;Oh, B. H.;Shim, S. C.;
  10. J. Heterocyclic Chem. v.37 Cho, C. S.;Oh, B. H.;Shim, S. C.;Oh, D. H.
  11. J. Heterocyclic Chem. v.36 Cho, C. S.;Oh, B. H.;Shim, S. C.
  12. Tetrahedron. v.56 Cho, C. S.;Kim, J. S.;Oh, B. H.;Kim, T. J.;Shim, S. C.;Yoon, N. S.
  13. Chem. Commun. Cho, C. S.;Oh, B. H.;Kim, J. S.;Kim, T. J..;Shim, S. C.
  14. Angew. Chem. Int. Ed. Engl. v.40 Cho, C. S.;Kim, B. T.;Lee, M. J.;Kim, T. J.;Shim, S. C.
  15. J. Am. Chem. Soc. v.95 Yoshimura, N.;Moritani, I.;Shimamura, T.;Murahashi, S. I.
  16. J. Am. Chem. Soc. v.100 Murahashi, S. I.;Hirano, T.;Yano, T. J.
  17. J. Am. Chem. Soc. v.100 Murahashi, S. I.;Hirano, T.;Yano, T.
  18. J. Chem. Soc. Chem. Commun. Shvo, Y.;Lanie, R. M.
  19. J. Organomet, Chem. v.208 Khai, B. T.;Concilio, C.;Porzi, G. J.
  20. J. Org. Chem. v.46 Khai, B. T.;Concilio, C.;Porzi, G.
  21. J. Organomet. Chem. v.231 Arcelli, A.;Khai, B. T.;Porzi, G.
  22. Tetrahedron Lett. v.23 Murahashi, S. I.;Kondo, K.;Hakata. T.
  23. J. Am. Chem. Soc. v.104 Laine, R. M.;Thomas, D. W.;Cary, L. W.
  24. Organometallics. v.2 Jung. C. W.;Fellmann, J.; D.;Garrou, P. E.
  25. Angew. Chem. Int. Ed. Engl. v.34 Murahashi, S. I.
  26. J. Am. Chem. Soc. Murahasi, S. I.;Yosshimura, N.;Tsumiyama, S. I.
  27. Tetrahedron Lett. v.25 Bellamy, F. D.;Ou, K.
  28. J. H. Chem. Rev. v.89 Holts, M. S.;Wilson, W. L.;Nelson.
  29. Chem. Rev. v.98 Naota, T.;Takaya, H.;Murahashi, S. I.

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