Dergiler / Turkish Journal of Chemistry / 2006 / Cilt: 30 - Sayı: 1

Synthesis of New 3-Pyrrolin-2-One Derivatives

Sayfa
125–130
Yayın Tarihi
2006-01-01
DOI
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This simple one-pot reaction furnished the corresponding pyrrolinones (3a-f) in acceptable yields.

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Amaç & Hipotez:Six new 3-pyrrolin-2-one derivatives were synthesized via the condensation reaction of amino acid esters (2a-f) with 2,5-dimethoxy-2,5-dihydrofurane (1) in acidic medium.
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Temel Bulgular & Veri:Six new 3-pyrrolin-2-one derivatives were synthesized via the condensation reaction of amino acid esters (2a-f) with 2,5-dimethoxy-2,5-dihydrofurane (1) in acidic medium.
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Sonuç & Katkı:This simple one-pot reaction furnished the corresponding pyrrolinones (3a-f) in acceptable yields.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Pyrrolinone · synthesis · dimethoxydihydrofurane

Özet

Six new 3-pyrrolin-2-one derivatives were synthesized via the condensation reaction of amino acid esters (2a-f) with 2,5-dimethoxy-2,5-dihydrofurane (1) in acidic medium. This simple one-pot reaction furnished the corresponding pyrrolinones (3a-f) in acceptable yields.

Abstract

Six new 3-pyrrolin-2-one derivatives were synthesized via the condensation reaction of amino acid esters (2a-f) with 2,5-dimethoxy-2,5-dihydrofurane (1) in acidic medium. This simple one-pot reaction furnished the corresponding pyrrolinones (3a-f) in acceptable yields.

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Bu Makaleye Atıf Yap

SAYGILI, N., ALTUNBAŞ, A., YEŞİLADA, A. (2006). Synthesis of New 3-Pyrrolin-2-One Derivatives. Turkish Journal of Chemistry, Cilt: 30 - Sayı: 1, 125–130. https://ajindex.com/articles/227792

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Kaynakça (18)

  1. D. Ma, J. Ma, W. Ding and L. Dai, Tetrahedron Asymmetry 7, 2365 (1996).
  2. G. Casiraghi, P. Spanu, G. Rassu, L. Pinna and F. Ulgheri, J. Org. Chem. 59, 2906 (1994).
  3. J.P. Dittami, F. Xu, H. Qi and M.W. Martin, Tetrahedron Lett. 36, 4201 (1995).
  4. R. Shiraki, A. Sumino, K. Tadano and S. Ogawa, J. Org. Chem. 61, 2845 (1996).
  5. F. Gavina, A.M. Costero, M.R. Andreu, M. Carda and S.V. Luis, J. Am. Chem. Soc. 110, 4017 (1988).
  6. J.P. Dittami, F. Xu, H. Qi and M.W. Martin, Tetrahedron Lett. 36, 4197 (1995).
  7. M. Yamamoto, H. Izukawa, M. Saiki and K. Yamada, J. Chem. Soc. Chem. Commun. 8, 560 (1988).
  8. E.G. Howard, R.V. Lindsey and C.W. Teobald, J. Am. Chem. Soc. 81, 4355 (1959).
  9. R.W. Franck and J. Auerbach, J. Org. Chem. 36, 31 (1971).
  10. F. Aydogan and A.S. Demir, Tetrahedron Asymmetry 15, 259 (2004).
  11. I. Baussanne, A. Chiaroni, H.P. Husson, C. Riche and J. Royer, Tetrahedron Lett. 35, 3931 (1994).
  12. I. Baussanne, C. Travers and J. Royer, Tetrahedron Asymmetry 9, 797 (1998).
  13. W.J. Koot, H. Hiemstra and W.N. Speckamp, Tetrahedron Asymmetry 4, 1941 (1993).
  14. W.J. Koot, H. Hiemstra and W.N. Speckamp, Tetrahedron Lett. 33, 7969 (1992).
  15. D.M. Cooper, R. Grigg, S. Hargreaves, P. Kennewell and J. Redpath, Tetrahedron 51, 7791 (1995).
  16. W.J. Koot, H. Hiemstra and W.N. Speckamp, J. Org. Chem. 57, 1059 (1992).
  17. R.A. Boissonnas, S. Guttmann and P.A. Jaquenoud, Helv. Chim. Acta 38, 1491, 1955.
  18. J.T. Baker and S. Sifniades, J. Org. Chem. 44, 2798 (1979).