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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 Full article

Journal Mendeleev Communications
ISSN: 0959-9436
Output data Year: 2018, Volume: 28, Number: 6, Pages: 584-586 Pages count : 3 DOI: 10.1016/j.mencom.2018.11.006
Authors Ustimenko Yulia P. 1 , Agafontsev Alexander M. 1 , Komarov Vladislav Yu. 2,3 , Tkachev Alexey V. 1,3
Affiliations
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

Abstract: 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.
Cite: 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 OpenAlex
Dates:
Published print: Nov 1, 2018
Identifiers:
Web of science: WOS:000455070900006
Scopus: 2-s2.0-85057738234
Elibrary: 38627410
OpenAlex: W2904519148
Citing:
DB Citing
Web of science 12
Scopus 12
Elibrary 12
OpenAlex 10
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