Literature DB >> 16294505

Efficient synthesis of isobenzofuran-1(3H)-ones (phthalides) and selected biological evaluations.

Ernst Bayer1, Safdar Hayat, M Iqbal Choudhary, Khalid Mohammed Khan, Syed Tasadaque Ali Shah, M Imran-ul-Haq, M Usman Anwar, Wolfgang Voelter.   

Abstract

The studies presented here deal with the convenient and efficient one-step conversion of o-alkylbenzoic acids into their corresponding isobenzofuran-1 (3H)-ones (phthalides) using NaBrO3/NaHSO3 in a two-phase system. A range of o-alkylbenzoic acids was used with the object of getting a variety of phthalide derivatives as multipurpose biologically active compounds. Seventeen phthalides have been synthesized and tested for cytotoxicity, antibacterial and antifungal activities. Some of these compounds showed promising cytotoxic effects against Artemia salina. Compounds 4j-4p were highly active against Gram-negative and Gram-positive bacteria among all tested compounds. In the fungicidal assay, the compounds showed a broad spectrum of activity against six fungi. All compounds were characterized via elemental analysis, UV, IR, mass and-NMR spectroscopy.

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Year:  2005        PMID: 16294505     DOI: 10.1055/s-0031-1296909

Source DB:  PubMed          Journal:  Arzneimittelforschung        ISSN: 0004-4172


  2 in total

1.  Synthesis of 1,4-dihydro-benzo[d][1,3]oxazin-2-ones from phthalides via an aminolysis-Hofmann rearrangement protocol.

Authors:  Eliud Hernández; Jessica M Vélez; Cornelis P Vlaar
Journal:  Tetrahedron Lett       Date:  2007-12-17       Impact factor: 2.415

2.  A phthalide derivative isolated from endophytic fungi Pestalotiopsis photiniae induces G1 cell cycle arrest and apoptosis in human HeLa cells.

Authors:  C Chen; R L Yang
Journal:  Braz J Med Biol Res       Date:  2013-07-30       Impact factor: 2.590

  2 in total

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