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http://elar.urfu.ru/handle/10995/26840
Полная запись метаданных
Поле DC | Значение | Язык |
---|---|---|
dc.contributor.author | Dudkin, S. | en |
dc.contributor.author | Iaroshenko, V. O. | en |
dc.contributor.author | Sosnovskikh, V. Y. | en |
dc.contributor.author | Tolmachev, A. A. | en |
dc.contributor.author | Villinger, A. | en |
dc.contributor.author | Langer, P. | en |
dc.date.accessioned | 2014-11-18T08:43:05Z | - |
dc.date.available | 2014-11-18T08:43:05Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Synthesis and reactivity of 5-polyfluoroalkyl-5-deazaalloxazines / S. Dudkin, V. O. Iaroshenko, V. Y. Sosnovskikh [et al.] // Organic and Biomolecular Chemistry. — 2013. — Vol. 11. — № 32. — P. 5351-5361. | en |
dc.identifier.issn | 1477-0520 | - |
dc.identifier.other | 1 | good_DOI |
dc.identifier.other | f1a29416-b4c3-4045-ba20-be696fa69c7c | pure_uuid |
dc.identifier.other | http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=84880861247 | m |
dc.identifier.uri | http://elar.urfu.ru/handle/10995/26840 | - |
dc.description.abstract | Reaction of 6-arylamino-1,3-dialkyluracils with anhydrides of polyfluorocarboxylic acids in the presence of pyridine and subsequent cyclization with concentrated H2SO4 gave the corresponding 1,3-dialkyl-5-(polyfluoroalkyl)pyrimido[4,5-b]quinoline-2,4(1H,3H)-diones (5-polyfluoroalkyl-5-deazaalloxazines). The reactivity of these compounds towards nucleophilic reagents, such as sodium cyanoborohydride, acetophenone, nitromethane, potassium cyanide, indole and p-thiocresol, as well as Suzuki and Sonogashira couplings are described. The nucleophilic addition takes place at the 5-position of the 5-deazaalloxazine system and is in many cases irreversible to give 5,10-dihydropyrimido[4,5-b]quinoline-2,4(1H,3H)-dione derivatives in good to excellent yields.© 2013 The Royal Society of Chemistry. | en |
dc.format.mimetype | application/pdf | en |
dc.language.iso | en | en |
dc.source | Organic and Biomolecular Chemistry | en |
dc.subject | ACETOPHENONES | en |
dc.subject | NITROMETHANE | en |
dc.subject | NUCLEOPHILIC ADDITIONS | en |
dc.subject | NUCLEOPHILIC REAGENT | en |
dc.subject | POTASSIUM CYANIDES | en |
dc.subject | SODIUM CYANOBOROHYDRIDE | en |
dc.subject | SONOGASHIRA COUPLING | en |
dc.subject | ADDITION REACTIONS | en |
dc.subject | KETONES | en |
dc.subject | SYNTHESIS (CHEMICAL) | en |
dc.subject | CYCLIZATION | en |
dc.subject | DRUG DERIVATIVE | en |
dc.subject | HETEROCYCLIC COMPOUND | en |
dc.subject | ISOALLOXAZINE | en |
dc.subject | PYRIDINE | en |
dc.subject | PYRIDINE DERIVATIVE | en |
dc.subject | QUINOLINE DERIVATIVE | en |
dc.subject | RIBOFLAVIN DERIVATIVE | en |
dc.subject | URACIL | en |
dc.subject | ALKYLATION | en |
dc.subject | ARTICLE | en |
dc.subject | CHEMISTRY | en |
dc.subject | CYCLIZATION | en |
dc.subject | HALOGENATION | en |
dc.subject | SYNTHESIS | en |
dc.subject | ALKYLATION | en |
dc.subject | AZA COMPOUNDS | en |
dc.subject | CYCLIZATION | en |
dc.subject | FLAVINS | en |
dc.subject | HALOGENATION | en |
dc.subject | PYRIDINES | en |
dc.subject | QUINOLINES | en |
dc.subject | URACIL | en |
dc.title | Synthesis and reactivity of 5-polyfluoroalkyl-5-deazaalloxazines | en |
dc.type | Article | en |
dc.type | info:eu-repo/semantics/publishedVersion | en |
dc.type | info:eu-repo/semantics/article | en |
dc.identifier.doi | 10.1039/c3ob26837c | - |
dc.identifier.scopus | 84880861247 | - |
local.affiliation | Institut für Chemie, Universität Rostock, Albert Einstein Str. 3a, 18059 Rostock, Germany | en |
local.affiliation | National Taras Shevchenko University, 62 Volodymyrska Str., 01033 Kyiv, Ukraine | en |
local.affiliation | Department of Chemistry, Ural Federal University, 51 Lenina Ave., 620000 Ekaterinburg, Russian Federation | en |
local.affiliation | Enamine Ltd, Alexandra Matrosova Street 23, Kyiv 01103, Ukraine | en |
local.affiliation | Leibniz-Institut für Katalyse an der Universität Rostock E.V., Albert Einstein Str. 29a, 18059 Rostock, Germany | en |
local.contributor.employee | Сосновских Вячеслав Яковлевич | ru |
local.description.firstpage | 5351 | - |
local.description.lastpage | 5361 | - |
local.issue | 32 | - |
local.volume | 11 | - |
dc.identifier.wos | 000322944900017 | - |
local.contributor.department | Институт естественных наук и математики | ru |
local.identifier.pure | 878889 | - |
local.identifier.eid | 2-s2.0-84880861247 | - |
local.identifier.wos | WOS:000322944900017 | - |
Располагается в коллекциях: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
Файлы этого ресурса:
Файл | Описание | Размер | Формат | |
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scopus-2013-0008.pdf | 404,97 kB | Adobe PDF | Просмотреть/Открыть |
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