Search results for: INDOLE

• Involve

  Journals

  ISSN: 1944-4176 , eISSN: 1944-4184

• Stereoselective Alkylation of Indole with 5-Arylidene-Meldrum’s Acids in the Presence of Organocatalysts

  Publication

  • S. Makowiec
  • K. Janikowska
  • A. Zakaszewska
  • E. Najda-Mocarska

  - LETTERS IN ORGANIC CHEMISTRY - Year 2018

  Background: Indole motif is frequently present in biologically active compounds. Enantiomerically pure or enriched 2,2-dimethyl-5-(aryl(1H-indol-3-yl)methyl)-1,3-dioxane-4,6-diones can be considered as a convenient starting point for the synthesis of a indole ring fused with cyclic ketones with biological activity. Preparation of chiral 2,2-dimethyl-5-(aryl(1H-indol-3-yl)methyl)-1,3-dioxane- 4,6-diones requires the reaction of...

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• INDOOR AND BUILT ENVIRONMENT

  Journals

  ISSN: 1420-326X , eISSN: 1423-0070

• Basic Income Studies

  Journals

  ISSN: 2194-6094 , eISSN: 1932-0183

• Journal of Fixed Income

  Journals

  ISSN: 1059-8596

• REVIEW OF INCOME AND WEALTH

  Journals

  ISSN: 0034-6586 , eISSN: 1475-4991

• Indole-Acrylonitrile Derivatives as Potential Antitumor and Antimicrobial Agents—Synthesis, In Vitro and In Silico Studies

  Publication

  • A. Kornicka
  • K. Gzella
  • K. Garbacz
  • M. Jarosiewicz
  • M. Gdaniec
  • J. Fedorowicz
  • L. Balewski
  • J. Kokoszka
  • A. Ordyszewska

  - Pharmaceuticals - Year 2023

  A series of 2-(1H-indol-2-yl)-3-acrylonitrile derivatives, 2a–x, 3, 4a–b, 5a–d, 6a–b, and 7, were synthesized as potential antitumor and antimicrobial agents. The structures of the prepared compounds were evaluated based on elemental analysis, IR, 1H- and 13NMR, as well as MS spectra. X-ray crystal analysis of the representative 2-(1H-indol-2-yl)-3-acrylonitrile 2l showed that the acrylonitrile double bond was Z-configured. All...

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• Synthesis of disubstituted 1,3,4,9-tetrahydropyrano-[3,4-b]indole-1-acetic acids derivatives

  Publication

  • A. S. Skwarecki

  - Year 2013

  1,3,4,9-tetrahydropyrano[3,4-b ]indole-1-acetic acid derivatives are of interest for pharmaceutical research as a core structure for synthesis of biological active substance - Etodolac (selective Cyclooxygenase-2 inhibitor, which belongs to the Non-steroidal Anti-inflammatory Drug, NSAID, that shows a clin-ically effective analgesic and anti-inflammatory activity). Here the way of synthesis of two 1,3,4,9-tetrahydropyrano[3,4-b...

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• The comparison of cytotoxic and genotoxic activities of glucosinolates, isothiocyanates, and indoles

  Publication

  • D. Kołodziejski
  • I. Koss-Mikołajczyk
  • H. Glatt
  • A. Bartoszek-Pączkowska

  - Scientific Reports - Year 2022

  Chemopreventive properties of Brassica vegetables are attributed mainly to their characteristic compounds—glucosinolates (GLs) and their main hydrolysis products—isothiocyanates (ITCs) and indoles. In this study, we compared antiproliferative activity (MTT test in HT29 cells) and genotoxic effects (comet assay in HT29 cells and restriction analysis in a cell-free system) of three GLs (sinigrin (SIN), glucotropaeolin (GTL), and...

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• General, Mild, and Metal-Free Functionalization of Indole and Its Derivatives Through Direct C3-Selenylation

  Publication

  • A. Hałuszczuk
  • N. Babul
  • Ł. Nierzwicki
  • W. Przychodzeń

  - EUROPEAN JOURNAL OF ORGANIC CHEMISTRY - Year 2019

  A very mild method for the introduction of functionalized alkylselenyl group at C-3 position of the indole ring was developed. The proposed procedure consists of an electrophilic substitution of indole and its derivatives with bis(O,O-diisopropoxyphosphorothioyl) diselenide and subsequent cleavage of the P–Se bond with tetrabutylammonium fluoride in the presence of various electrophilic reagents. This method can be successfully...

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