Selective cross-dehydrogenative C–O coupling of N-hydroxy compounds with pyrazolones. Introduction of the diacetyliminoxyl radical into the practice of organic synthesis Научная публикация
Журнал |
Organic chemistry frontiers
ISSN: 2052-4110 , E-ISSN: 2052-4129 |
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Вых. Данные | Год: 2017, Том: 4, Номер: 10, Страницы: 1947-1957 Страниц : 11 DOI: 10.1039/c7qo00447h | ||||||||||
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Реферат:
Oxidative C–O coupling of pyrazolones with N-hydroxy compounds of different classes (N-hydroxyphthalimide, N-hydroxybenzotriazole, oximes) was achieved; both one-electron oxidants (Fe(ClO4)3, (NH4)2Ce(NO3)6) and two-electron oxidants (PhI(OAc)2, Pb(OAc)4) are applicable, and the yields reach 91%. Apparently, the coupling proceeds via the formation of N-oxyl radicals from N-hydroxy compounds. One of the N-oxyl intermediates, the diacetyliminoxyl radical, was found to be exclusively stable in solution in spite of being sterically unhindered; it was isolated from an oxidant and used as a new reagent for the synthesis and mechanism study. The products of C–O coupling of pyrazolones with N-hydroxyphthalimide can be easily transformed into aminooxy compounds, valuable substances for combinatorial chemistry.
Библиографическая ссылка:
Krylov I.B.
, Paveliev S.A.
, Shelimov B.N.
, Lokshin B.V.
, Garbuzova I.A.
, Tafeenko V.A.
, Chernyshev V.V.
, Budnikov A.S.
, Nikishin G.I.
, Terent'ev A.O.
Selective cross-dehydrogenative C–O coupling of N-hydroxy compounds with pyrazolones. Introduction of the diacetyliminoxyl radical into the practice of organic synthesis
Organic chemistry frontiers. 2017. V.4. N10. P.1947-1957. DOI: 10.1039/c7qo00447h WOS Scopus OpenAlex
Selective cross-dehydrogenative C–O coupling of N-hydroxy compounds with pyrazolones. Introduction of the diacetyliminoxyl radical into the practice of organic synthesis
Organic chemistry frontiers. 2017. V.4. N10. P.1947-1957. DOI: 10.1039/c7qo00447h WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: | WOS:000411716700008 |
Scopus: | 2-s2.0-85030108680 |
OpenAlex: | W2737052919 |