Selective and efficient electrocatalytic way to spirobarbituric dihydrofurans Научная публикация
| Журнал |
Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436 |
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| Вых. Данные | Год: 2021, Том: 31, Номер: 3, Страницы: 347-349 Страниц : 3 DOI: 10.1016/j.mencom.2021.04.021 | ||
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| Организации |
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Реферат:
Electrocatalytic cyclization of 6-hydroxy-5-[(2-hydroxy-6-oxocyclohex-1-en-1-yl)(aryl)methyl]-1,3-dimethylpyrimidine-2,4-(1H,3H)-diones in alcohols in an undivided cell in the presence of sodium halides results in selective formation of substituted spirobarbituric dihydrofurans in 82–93% yields. Crystal structure of 3-(3-bromophenyl)-1′,3′,6,6-tetramethyl-3,5,6,7-tetrahydro-2′,4-dihydrospiro[benzofuran-2,5′-pyrimidine]-2′,4,4′,6′(1′H,3′H)-tetraone has been confirmed by X-ray diffraction data.
Библиографическая ссылка:
Elinson M.N.
, Vereshchagin A.N.
, Ryzhkova Y.E.
, Egorov M.P.
Selective and efficient electrocatalytic way to spirobarbituric dihydrofurans
Mendeleev Communications. 2021. V.31. N3. P.347-349. DOI: 10.1016/j.mencom.2021.04.021 Scopus OpenAlex
Selective and efficient electrocatalytic way to spirobarbituric dihydrofurans
Mendeleev Communications. 2021. V.31. N3. P.347-349. DOI: 10.1016/j.mencom.2021.04.021 Scopus OpenAlex
Идентификаторы БД:
| Scopus: | 2-s2.0-85107150933 |
| OpenAlex: | W3172193702 |