Synthesis of chiral nopinane annelated 3-methyl-1-aryl-1H-pyrazolo[3,4-b]pyridines by condensation of pinocarvone oxime with 1-aryl-1H-pyrazol-5-amines

Synthesis of chiral nopinane annelated 3-methyl-1-aryl-1H-pyrazolo[3,4-b]pyridines by condensation of pinocarvone oxime with 1-aryl-1H-pyrazol-5-amines Научная публикация

Журнал

Mendeleev Communications
ISSN: 0959-9436

Вых. Данные

Год: 2018, Том: 28, Номер: 6, Страницы: 584-586 Страниц : 3 DOI: 10.1016/j.mencom.2018.11.006

Авторы

Ustimenko Yulia P. ¹ , Agafontsev Alexander M. ¹ , Komarov Vladislav Yu. ^2,3 , Tkachev Alexey V. ^1,3

Организации

1	(Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia
2	(Данные Web of science) Russian Acad Sci, AV Nikolaev Inst Inorgan Chem, Siberian Branch, Novosibirsk 630090, Russia
3	(Данные Web of science) Novosibirsk State Univ, Dept Nat Sci, Novosibirsk 630090, Russia

Chiral 1H-pyrazolo[3,4-b]pyridines fused with nopinane frame were obtained by FeCl3-catalyzed assembling of pinocarvone oxime and 1-aryl-1H-pyrazol-5-amines. Chemical structures of new compounds were solved by NMR spectroscopy and confirmed by quantum chemical calculations and X-ray crystallography.

Ustimenko Y.P. , Agafontsev A.M. , Komarov V.Y. , Tkachev A.V.
Synthesis of chiral nopinane annelated 3-methyl-1-aryl-1H-pyrazolo[3,4-b]pyridines by condensation of pinocarvone oxime with 1-aryl-1H-pyrazol-5-amines
Mendeleev Communications. 2018. V.28. N6. P.584-586. DOI: 10.1016/j.mencom.2018.11.006 WOS Scopus РИНЦ

Опубликована в печати:

1 нояб. 2018 г.

Web of science	WOS:000455070900006
Scopus	2-s2.0-85057738234
РИНЦ	38627410
OpenAlex	W2904519148