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A simple and efficient approach to one-pot synthesis of mono- and bis-N-aryl-3-aminodihydropyrrol-2-one-4-carboxylates catalyzed by InCl_3 被引量:1

A simple and efficient approach to one-pot synthesis of mono- and bis-N-aryl-3-aminodihydropyrrol-2-one-4-carboxylates catalyzed by InCl_3
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摘要 An efficient and straightforward procedure has been developed for the synthesis of highly substituted mono- and bis-N-aryl-3-aminodihydropyrrol-2-one-4-carboxylates via a one-pot, four-component domino reaction of amines, dialkyl acetylenedicarboxylates and formaldehyde in the presence of InCl3 (20 mol%) in MeOH at ambient temperature. The salient advantages of this method are mild reaction conditions, environmentally benign, high to excellent yields, shorter reaction times, easy operation and no column chromatographic separation. An efficient and straightforward procedure has been developed for the synthesis of highly substituted mono- and bis-N-aryl-3-aminodihydropyrrol-2-one-4-carboxylates via a one-pot, four-component domino reaction of amines, dialkyl acetylenedicarboxylates and formaldehyde in the presence of InCl3 (20 mol%) in MeOH at ambient temperature. The salient advantages of this method are mild reaction conditions, environmentally benign, high to excellent yields, shorter reaction times, easy operation and no column chromatographic separation.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2014年第1期58-60,共3页 中国化学快报(英文版)
基金 support from the Research Council of University of Sistan and Baluchestan and Payame Noor University
关键词 Dihydropyrrol-2-one Heterocycle InCl3 Four-component reaction Dihydropyrrol-2-one Heterocycle InCl3 Four-component reaction
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  • 1H. Kakeya, C. Onozawa, M. Sato, et al. J. Med. Chem. 40 (1997) 391.
  • 2B.A. Kulkarani, A. Ganesan, Angew. Chem. Int. Ed. Engl. 36 (1997) 2454.
  • 3S. Bienz, C. Busacca, A.I. Mayers, J. Am. Chem. Soc. 111 (1989) 1905.
  • 4B. Tarnchompoo, C. Thebtaranonth, Y. Thebtaranonth, Tetrahedron Lett. 28 (1987) 6675.
  • 5J. Barluenga, E Palacios, S. Fustero, et al. Synthesis (1981) 200.
  • 6J.T. Baker, S, Sifniades, J. Org, Chem, 44 (1979) 2798.
  • 7W.J. Moree, G.A. van der Marel, R.M.J. Liskamp, Tetrahedron Lett. 32 (1991) 409.
  • 8J.L. Radkiewicz, M.A. McAllister, E. Goldstein, et al. J. Org. Chem. 63 (1998) 1419.
  • 9D.K. Jones-Hertzog, W.L. Jorgensen, J. Med. Chem. 40 (1997) 1539.
  • 10I. Yavari, N. Zabarjad-Shiraz, H.R. Bijanzadeh, Phosphorus Sulfur Silicon 179 (2004) 1381.

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