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Synthesis and structure of novel ylidene derivatives of methanobenzo[g]thiazolo[2,3-d][1,3,5]oxadiazocine Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Вых. Данные Год: 2016, Том: 52, Номер: 5, Страницы: 331-336 Страниц : 6 DOI: 10.1007/s10593-016-1886-7
Ключевые слова diastereomers; methanobenzo[g]thiazolo[2,3-d][1,3,5]oxadiazocines; ylidenes; antidiabetic activity; NMR spectroscopy; X-ray structural analysis
Авторы Kulakov Ivan V. 1 , Ogurtsova Diana N. 1 , Shulgau Zarina T. 2 , Seilkhanov Tulegen M. 3 , Gatilov Yurii V. 4,5
Организации
1 (Данные Web of science) FM Dostoevskii Omsk State Univ, 55a Mir Ave, Omsk 644077, Russia
2 (Данные Web of science) Republican State Enterprise Natl Ctr Biotechnol, 13-5 Kurgalzhynskoe Rd, Astana 010000, Kazakhstan
3 (Данные Web of science) Kokshetau State Univ, 76 Abay St, Kokshetau 020000, Kazakhstan
4 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Akad Lavrientieva Ave, Novosibirsk 630090, Russia
5 (Данные Web of science) Novosibirsk State Univ, 2 Pirogov St, Novosibirsk 630090, Russia

Реферат: Novel benzylidene and furylidene derivatives of tricyclic thiazolo[2,3-d][1,3,5]oxadiazocines were synthesized, and their structures were confirmed by H-1 and C-13 NMR spectroscopy. It was shown that ylidene derivatives of 11H-5,11,5-pentane-[1,1,5]triyl[1,3]thiazolo[2,3-d][1,3,5]oxadiazocin-1-one are obtained as a mixture of Z- and E-isomers. Recrystallization of the isomer mixture affords the major Z-isomer, structure of which has been established by X-ray structural analysis.
Библиографическая ссылка: Kulakov I.V. , Ogurtsova D.N. , Shulgau Z.T. , Seilkhanov T.M. , Gatilov Y.V.
Synthesis and structure of novel ylidene derivatives of methanobenzo[g]thiazolo[2,3-d][1,3,5]oxadiazocine
Chemistry of Heterocyclic Compounds. 2016. V.52. N5. P.331-336. DOI: 10.1007/s10593-016-1886-7 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 мая 2016 г.
Опубликована online: 1 июл. 2016 г.
Идентификаторы БД:
Web of science: WOS:000379813800012
Scopus: 2-s2.0-85028260845
РИНЦ: 41788132
OpenAlex: W2470938351
Цитирование в БД:
БД Цитирований
Web of science 2
Scopus 2
РИНЦ 3
OpenAlex 2
Альметрики: