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Synthesis of some butenolides and study of their antibacterial activity

Autorzy
Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Butenolides and their analogues represent a wide range of natural compounds of a medical and biological importance. In the last decades, a great number of compounds of various structures, in general from Alkylidene butenolide, were isolated and showed biological activities. In this work we have studied the reactivity of some alkylidene butenolide and their antibacterial activity. the study is of a scientific interest in terms of the synthesis of new compounds (Butenolide 01: 5-hydroxy-5-(1-methoxypropan-2-yl)-4-methylfuran-2(5H)-one, Butenolide 02: 5-(1-methoxypropan-2-yl)-4-methylfuran-2(5H)-one) that have not been studied before by other researchers; and of an economic importance because of its synthesis process which is easy and inexpensive. Moreover, butenolide showed a positive antimicrobial activity (antibiotic) against pathogenic bacteria (mainly Enterobacter hafniae).
Rocznik
Strony
61--67
Opis fizyczny
Bibliogr. 17 poz., rys., tab., wykr.
Twórcy
autor
  • Laboratoire de Valorisation et Technologie des Ressources Sahariennes, Département Sciences de la Matière, Institut des Sciences et Technologie, Centre Universitaire d'El-Oued, B.P. 789 El-Oued 39000, Algerie
autor
  • Laboratoire de Valorisation et Technologie des Ressources Sahariennes, Département Sciences de la Matière, Institut des Sciences et Technologie, Centre Universitaire d'El-Oued, B.P. 789 El-Oued 39000, Algerie
Bibliografia
  • [1] Xu C., Negishi E., Tetrahedron Lett. 40 (1999) 431.
  • [2] Ma S., Shi Z., J. Org. Chem. 63 (1998) 6387.
  • [3] Rossi R., Bellina F., Biagetti M., Mannina L., Tetrahedron Lett. 39 (1998) 7799.
  • [4] Rossi R., Bellina F., Biagetti M., Mannina L., Tetrahedron Lett. 39 (1998) 7599.
  • [5] Rossi R., Bellina F., Mannina L., Tetrahedron Lett. 39 (1998) 3017.
  • [6] Rossi R., Bellina F., Bechini C., Mannina L., Verganini P., Tetrahedron 54 (1998) 135.
  • [7] Liu F., Negishi E., J. Org. Chem. 62 (1997) 8591.
  • [8] Marshall J. A., Wolf M. A., Wallace E. M., J. Org. Chem. 62 (1997) 367.
  • [9] Rao Y. S., Chem. Rev. 76 (1976) 625.
  • [10] Rao Y. S., Chem. Rev. 64 (1964) 353.
  • [11] Negishi E., Kotora M., Tetrahedron 53 (1997) 6707.
  • [12] Von der Ohe F., Brückner R., Tetrahedron Lett. 39 (1998) 1909-1910.
  • [13] Jorgensen J. H., Ferraro M., J. Clin. Infect. Dis. 26 (1998) 973-980 .
  • [14] Robert-Dernuet S., (Editeur: Décarie Vigot), Antibiotiques et antibiogrammes, Montréal, Paris 1995, p. 322.
  • [15] Ericsson H. M. O., Sherris. J. C., Antibiotic Sensitivity Testing, Report of an International Collaborative Study. -Actes. path. Microbiol. Scand., B Suppl., 1971, pp. 90, 217.
  • [16] Baurer A. W., Kirry W. M. M., Sherries J. C. A., Turch M., Amer J. Clin. Pathol. 45 (1966) 493-496 .
  • [17] L'antibiogramme: Principes, Méthodologie, Intérêt et Limites. Journées nationales GVT-INRA Guerin Faublée V., Carret C., 1999, pp. 5-12 .
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-180ad0ca-25e1-4a2a-b020-538b59b7e7d1
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