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Cascade Assembling of Isatins and Barbituric Acids: Facile and Efficient Way to 2′′H‐Dispiro[indole‐3,5′‐furo[2,3‐d]pyrimidine‐6′,5′′‐pyrimidine]‐2,2′,2′′,4′,4′′,6′′‐(1H,1′H,1′′H,3′H,3′′H)‐hexone Scaffold Научная публикация

Журнал Journal of Heterocyclic Chemistry
ISSN: 0022-152X , E-ISSN: 1943-5193
Вых. Данные Год: 2013, Том: 50, Номер: 5, Страницы: 1236-1241 Страниц : 6 DOI: 10.1002/jhet.1699
Авторы Elinson Michail N. 1 , Merkulova Valentina M. 1 , Ilovaisky Alexey I. 1 , Nikishin Gennady I. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Leninsky prospect 47, 119991 Moscow, Russia

Реферат: “One-pot” transformation of isatins and barbituric acids by the direct action of the only bromine in ethanol results in the formation of substituted 2′′H-dispiro[indole-3,5′-furo[2,3-d]pyrimidine-6′,5′′-pyrimidine]-2,2′,2′′,4′,4′′,6′′-(1H,1′H,1′′H,3′H,3′′H)-hexones in 70–87% yields via complex cascade process. Dispirobarbiturates containing spiro indole and furo[2,3-d]pyrimidine framework are a class of compounds with prominent pharmacological and physiological activity. Thus, seven previously inaccessible 2′′H-dispiro[indole-3,5′-furo[2,3-d]pyrimidine-6′,5′′-pyrimidine]-2,2′,2′′,4′,4′′,6′′-(1H,1′H,1′′H,3′H,3′′H)-hexones have been synthesized that represent the new class of dispirobarbiturates.
Библиографическая ссылка: Elinson M.N. , Merkulova V.M. , Ilovaisky A.I. , Nikishin G.I.
Cascade Assembling of Isatins and Barbituric Acids: Facile and Efficient Way to 2′′H‐Dispiro[indole‐3,5′‐furo[2,3‐d]pyrimidine‐6′,5′′‐pyrimidine]‐2,2′,2′′,4′,4′′,6′′‐(1H,1′H,1′′H,3′H,3′′H)‐hexone Scaffold
Journal of Heterocyclic Chemistry. 2013. V.50. N5. P.1236-1241. DOI: 10.1002/jhet.1699 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000325939000038
Scopus: 2-s2.0-84884903415
OpenAlex: W2950144912
Цитирование в БД:
БД Цитирований
OpenAlex 12
Scopus 12
Web of science 11
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