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Highly efficient and eco-friendly one-pot synthesis of penta substitute pyrrole derivatives under catalyst-free conditions

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
An eco-friendly and efficient one-pot synthesis of penta-substituted pyrrole derivatives via a four-component reaction of maldrum’s acid, arylglyoxal monohydrate, dimethyl but-2-yne-dioate and amines under catalyst-free conditions in an environmentally friendly medium is described. The simple experimental procedure, catalyst-free reaction conditions, short period of conversion, and excellent yields are the advantages of the present method. Good chemical yields have been achieved without the need for chromatography and recrystallization or other purification methods.
Rocznik
Strony
257--264
Opis fizyczny
Bibliogr. 10 poz., tab., wz.
Twórcy
  • Department of Chemistry (UGC-SAP & DST-FIST Sponsored), Saurashtra University, Rajkot -360005, Gujarat, India National Facility for Drug Discovery Center, Saurashtra University, Rajkot -360005, Gujarat, India
autor
  • Department of Chemistry (UGC-SAP & DST-FIST Sponsored), Saurashtra University, Rajkot -360005, Gujarat, India National Facility for Drug Discovery Center, Saurashtra University, Rajkot -360005, Gujarat, India
autor
  • Department of Chemistry (UGC-SAP & DST-FIST Sponsored), Saurashtra University, Rajkot -360005, Gujarat, India National Facility for Drug Discovery Center, Saurashtra University, Rajkot -360005, Gujarat, India
  • Department of Chemistry (UGC-SAP & DST-FIST Sponsored), Saurashtra University, Rajkot -360005, Gujarat, India National Facility for Drug Discovery Center, Saurashtra University, Rajkot -360005, Gujarat, India
autor
  • Department of Chemistry (UGC-SAP & DST-FIST Sponsored), Saurashtra University, Rajkot -360005, Gujarat, India National Facility for Drug Discovery Center, Saurashtra University, Rajkot -360005, Gujarat, India
Bibliografia
  • [1] B. Thompson, J. Montgomery, Org. Lett. 13 (2011) 3289.
  • [2] B. Trost, A. Gutierrez, R. Livingston, Org. Lett. 11 (2009) 2539.
  • [3] N. Ganguly, S. Roy, P. Mondal, R. Saha, Tetrahedron Lett. 53 (2012) 7067.
  • [4] L. Wen, Y. Shi, G. Liu, Org. Chem. 77 (2012) 4252.
  • [5] D. Hong, Y. Zhu, Y. Li, X.Lin, P. Lu ,Y. Wang, Org. Lett. 13 (2011) 4668.
  • [6] B. Lee, M. Clothier, F. Dutton, G. Conder, S. Johnson, Bioorg. Med.Chem. Lett. 8 (1998) 3317.
  • [7] J. Jung, Y. Jung, O. Park, Synth. Commun. 31(2001) 1195.
  • [8] S. Hesse G. Kirsch, Tetrahedron Lett. 43 (2002) 1213.
  • [9] J. Jung, J. Lee, S. Oh, J. Lee, O. Park, Bioorg. Med. Chem. Lett. 14 (2004) 5527.
  • [10] G. Melagraki, A. Afantitis, O. Igglessi-Markopoulou, A. Detsi, M. Koufaki, C. Kontogiorgis, D. J. Hadjipavlou-Litina, Eur. J. Med. Chem. 44 (2009) 3020.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-d71c2d37-a262-48b0-a1ea-ef9e790369b1
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