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Heteroannelations with pinane-derived ß-enaminoaldehyde Full article

Journal Heterocyclic Communications
ISSN: 0793-0283
Output data Year: 2000, Volume: 6, Number: 4, Pages: 327-332 Pages count : 6
Authors Popov S.A. 1 , Tkachev A.V. 1
Affiliations
1 (Scopus) Department of Natural Sciences, Novosibirsk State University, Novosibirsk Inst. of Organ. Chem., Academician Lavrentjev Ave. 9, Novosibirsk, 630090, Russian Federation

Abstract: Synthesis of new chiral fused pyridines and pyrimidines with pinane carbon frame prospective as bioactive compounds is described. Heterocylisations of pinane-derived ß-enaminoaldehyde, need generally more rigid conditions than for o-aminobenzaldehyde, probably, both due to sterical and electronic reasons.
Cite: Popov S.A. , Tkachev A.V.
Heteroannelations with pinane-derived ß-enaminoaldehyde
Heterocyclic Communications. 2000. V.6. N4. P.327-332. WOS Scopus РИНЦ
Identifiers:
Web of science: WOS:000090119700008
Scopus: 2-s2.0-0034366619
Elibrary: 13354549
Citing:
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Scopus 2
Web of science 2
Elibrary 3