Synthesis, structure, and some transformations of novel 1,5-methanonapto[1,2-g][1,3,5]oxadiazocine derivatives Научная публикация
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Journal of Heterocyclic Chemistry
ISSN: 0022-152X , E-ISSN: 1943-5193 |
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| Вых. Данные | Год: 2018, Том: 55, Номер: 4, Страницы: 923-928 Страниц : 6 DOI: 10.1002/jhet.3119 | ||||||||||
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Реферат:
Biginelli reaction of thiourea, 2-hydroxy-1-naphthaldehyde, and acetoacetic ester (or benzoyl acetone) under solvent-free conditions and MW irradiation gave novel 3-thioxo-2,3,4,5-tetrahydro-1H-1,5-methanonaphtho[1,2-g][1,3,5]oxadiazocine derivatives. Subsequent reaction of the obtained compounds with α-chloroacetamide led to 5-methyl-5H,13H-5,13-methanonaphtho[1,2-g] thiazolo[2,3-d][1,3,5]oxadiazocin-1(2H)-ones, which were converted to the Z-isomers of 2-arylylidene-5H,13H-5,13-methanonaphtho[1,2-g]thiazolo[2,3-d][1,3,5]oxadiazocin-1(2H)-one derivatives by reaction with arylaldehydes. The structures of the products were characterized by 1H NMR, 13C NMR spectra, and X-ray analysis.
Библиографическая ссылка:
Kulakov I.V.
, Ogurtsova D.N.
, Seilkhanov T.M.
, Gatilov Y.V.
, Fisyuk A.S.
Synthesis, structure, and some transformations of novel 1,5-methanonapto[1,2-g][1,3,5]oxadiazocine derivatives
Journal of Heterocyclic Chemistry. 2018. V.55. N4. P.923-928. DOI: 10.1002/jhet.3119 WOS Scopus РИНЦ OpenAlex
Synthesis, structure, and some transformations of novel 1,5-methanonapto[1,2-g][1,3,5]oxadiazocine derivatives
Journal of Heterocyclic Chemistry. 2018. V.55. N4. P.923-928. DOI: 10.1002/jhet.3119 WOS Scopus РИНЦ OpenAlex
Даты:
| Поступила в редакцию: | 5 сент. 2017 г. |
| Опубликована online: | 9 февр. 2018 г. |
Идентификаторы БД:
| Web of science: | WOS:000430179800017 |
| Scopus: | 2-s2.0-85041721298 |
| РИНЦ: | 35485462 |
| OpenAlex: | W2791105809 |