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Постійне посилання колекціїhttps://dspace.nuft.edu.ua/handle/123456789/7522

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Зараз показуємо 1 - 9 з 9
  • Ескіз
    Документ
    Aminomethylation of formononetin and cladrin by primary amines
    (2009) Bondarenko, Svetlana; Frasinyuk, Mihaylo; Khilya, Volodimir
    The reaction of natural isoflavones formononetin and cladrin with primary amines and formalin in the presence of a base catalyst was studied. Several novel substituted 9,10-dihydro-4H,8H-chromeno[8,7-e][1,3]oxazin-4-ones containing alkyl, benzyl, or heterylalkyl substituents in the N-9 position were synthesized.
  • Ескіз
    Документ
    Synthesis and properties of 4-(3-amino-2-benzofuranyl)-coumarins
    (2009) Frasinyuk, Mihaylo; Gorelov, S.; Bondarenko, Svetlana; Khilya, Volodimir
    The alkylation of o-cyanophenol by 4-chloromethylcoumarins and subsequent intramolecular condensation by the cyano and methylene groups gives substituted 4-(3-amino-2-benzofuranyl) coumarins. We studied the reactions of these compounds with acylating agents as well as with aldehydes, which lead to the 6H-[1]benzofuro[3,2-b]chromeno[4,3-d]pyridin-6-one system as the result of consecutive transformations.
  • Ескіз
    Документ
    Synthesis and properties of 4-chloromethyl-6-hydroxycoumarins and 4-(2-benzofuryl)-6-hydroxycoumarins
    (2009) Frasinyuk, Mihaylo; Bondarenko, Svetlana; Khilya, Volodimir
    New 4-chloromethyl-6-hydroxycoumarins have been obtained by the condensation of hydroquinone derivatives with 4-chloroacetoacetic ester, and have been used for the synthesis of 4-(2-benzofuryl)-6-hydroxycoumarins. Alkylation and acylation of the phenolic hydroxyl of the synthesized 4-(2-benzofuryl)coumarins have been investigated.
  • Ескіз
    Документ
    Reaction of analogs of natural isoflavonoids with amidines
    (2006) Frasinyuk, Mihaylo; Bondarenko, Svetlana; Khilya, Volodimir
    Recyclization of the chromone ring in a series of analogs of natural isoflavonoids by reaction with amidines was studied.
  • Ескіз
    Документ
    Synthesis of formononetin analogs
    (2003) Bondarenko, Svetlana; Frasinyuk, Mihaylo; Khilya, Volodimir
    Derivatives of the natural isoflavone formononetin were synthesized. Acylation and alkylation of the phenolic hydroxyls and the chromone ring were investigated.
  • Ескіз
    Документ
    Synthesis of 3',4'-dimethoxyisoflavone derivatives
    (2003) Bondarenko, Svetlana; Frasinyuk, Mihaylo; Khilya, Volodimir
    2-(Un)substituted-3',4'-dimethoxy-7-hydroxyisoflavones were synthesized. Their derivatives substituted at the phenolic hydroxyl were prepared by alkylation and acylation. Aminomethyl derivatives were also prepared.
  • Ескіз
    Документ
    Synthesis of pseudobaptigenin analogs
    (2003) Bondarenko, Svetlana; Frasinyuk, Mihaylo; Khilya, Volodimir
    Homologs of the natural isoflavonoid pseudobaptigenin containing benzodioxane and benzodioxepane fragments were synthesized. Methanesulfonyl, carbamoyl, aminomethyl, and coumarin-containing isoflavone derivatives were prepared.
  • Ескіз
    Документ
    Aminomethylation of 3-aryl-7-hydroxycoumarins
    (2010) Bondarenko, Svetlana; Frasinyuk, Mihaylo; Khilya, Volodimir
    The reaction of the analogs of natural 3-arylbenzopyran-2-ones with electrophilic reagents of aminal structure was studied. Substituted 8-aminomethyl-3-aryl-7-hydroxycoumarins were synthesized. The optimum conditions were determined for the production of 9-alkyl- and 9-(het)arylmethyl derivatives of 3-aryl-9,10-dihydro-2H,8H-chromeno[8,7-e][1,3]oxazin-2-one in the series of analogs of natural 3-arylbenzopyran-2-ones.
  • Ескіз
    Документ
    Features of the aminomethylation of 7-hydroxy-4'-fluoroisoflavones with primary amines
    (2010) Bondarenko, Svetlana; Frasinyuk, Mihaylo; Khilya, Volodimir
    The behavior of 7-hydroxy-4'-fluoroisoflavones under the conditions of the Mannich reaction with primary amines was studied. New 9-alkyl-substituted 3-(4-fluorophenyl)-9,10-dihydro-4H,8H-chromeno-[8,7-e][1,3]oxazin-4-ones were synthesized. A method was developed for the synthesis of 8-amino- methyl derivatives of isoflavones.