Autor:	E. T. Oganesyan, D. E. Tvorovskii, Yu. A. Mal'tsev
Rok vydání:	2001
Předmět:	chemistry.chemical_classification chemistry.chemical_compound chemistry Computational chemistry Flavone derivatives Radical Hydroxy group Hydroxyl radical Reactivity (chemistry) General Chemistry Radical cyclization Flavones
Zdroj:	Russian Journal of General Chemistry. 71:939-944
ISSN:	1070-3632
DOI:	10.1023/a:1012395821594
Popis:	Semiempirical quantum-chemical calculations were used to study the reactivity of the C2 = C3 bond in flavones in reaction with hydroxyl radical. The preferred pathway was found to be addition of the radical by C3. Increased reactivity in the reaction in question of the hydroxy groups on C3 and C4' in polyhydroxyflavones was revealed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::8f13611d532daedf4815f59363a4157c https://doi.org/10.1023/a:1012395821594 Zobrazit plný text záznamu Full text from SpringerLink