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New approach to the synthesis of substituted 7H‐furo[3,2‐b]pyran‐7‐ones based on 5‐hydroxy‐2‐methyl‐4H‐pyran‐4‐one derivatives Научная публикация

Журнал Journal of Heterocyclic Chemistry
ISSN: 0022-152X , E-ISSN: 1943-5193
Вых. Данные Год: 2019, Том: 56, Номер: 11, Страницы: 3081-3087 Страниц : 7 DOI: 10.1002/jhet.3706
Авторы Komogortsev Andrey N. 1 , Lichitsky Boris V. 1 , Tretyakov Alexander D. 1 , Fakhrutdinov Artem N. 1 , Dudinov Arkady A. 1 , Krayushkin Michail M. 1
Организации
1 N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia

Реферат: A convenient approach to the synthesis of the previously unknown 7H-furo[3,2-b]pyran-7-ones based on the intramolecular cyclization of carbonyl derivatives of 5-hydroxy-2-methyl-4H-pyran-4-one has been elaborated. Key intermediates in the synthesis of the target 7H-furo[3,2-b]pyran-7-ones are 3-hydroxy-6-methyl-2-(2-oxo-2-arylethyl)-4H-pyran-4-ones. They are formed as a result of multicomponent condensation of 5-hydroxy-2-methyl-4H-pyran-4-one with arylglyoxals and 4-methoxyaniline.
Библиографическая ссылка: Komogortsev A.N. , Lichitsky B.V. , Tretyakov A.D. , Fakhrutdinov A.N. , Dudinov A.A. , Krayushkin M.M.
New approach to the synthesis of substituted 7H‐furo[3,2‐b]pyran‐7‐ones based on 5‐hydroxy‐2‐methyl‐4H‐pyran‐4‐one derivatives
Journal of Heterocyclic Chemistry. 2019. V.56. N11. P.3081-3087. DOI: 10.1002/jhet.3706 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000485076400001
Scopus: 2-s2.0-85071744558
OpenAlex: W2971831692
Цитирование в БД:
БД Цитирований
OpenAlex 15
Scopus 15
Web of science 15
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