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MICROWAVE-ASSISTED SYNTHESIS OF CHIRAL NOPINANE-ANNELATED PYRIDINES BY CONDENSATION OF PINOCARVONE OXIME WITH ENAMINES PROMOTED BY FeCl3 AND CuCl2 Full article

Journal Synthetic Communications
ISSN: 0039-7911 , E-ISSN: 1532-2432
Output data Year: 2014, Volume: 44, Number: 12, Pages: 1817-1824 Pages count : DOI: 10.1080/00397911.2013.877145
Tags Emanimes; microwave; oxime; pyridines; terpenoids; transition metals
Authors Vasilyev Eugene S. 1 , Agafontsev Alexander M. 1 , Tkachev Alexey V. 1,2
Affiliations
1 (Данные Web of science) Novosibirsk Organ Chem Inst, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Dept Nat Sci, Novosibirsk 630090, Russia

Abstract: Reaction of pinocarvone oxime with enamines and FeCl3 or CuCl2 resulted in annulation of nopinane carbon frame with pyridine and regioselective formation of chiral nopinane-annelated pyridines in 20-39% yields. Chemical structure of the pyridine derivatives were proved by precise NMR study.
Cite: Vasilyev E.S. , Agafontsev A.M. , Tkachev A.V.
MICROWAVE-ASSISTED SYNTHESIS OF CHIRAL NOPINANE-ANNELATED PYRIDINES BY CONDENSATION OF PINOCARVONE OXIME WITH ENAMINES PROMOTED BY FeCl3 AND CuCl2
Synthetic Communications. 2014. V.44. N12. P.1817-1824. DOI: 10.1080/00397911.2013.877145 WOS Scopus РИНЦ OpenAlex
Files: Full text from publisher
Dates:
Published online: May 14, 2014
Published print: Jun 18, 2014
Identifiers:
Web of science: WOS:000337973400010
Scopus: 2-s2.0-84901372982
Elibrary: 22214146
OpenAlex: W2951235081
Citing:
DB Citing
Web of science 15
Scopus 17
Elibrary 17
OpenAlex 18
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