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Polyalkoxybenzenes from plant material 6. Synthesis of 3-methyl-3,4-dihydroisoquinolines from apiol Full article

Journal Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Output data Year: 2012, Volume: 61, Number: 8, Pages: 1627-1630 Pages count : 4 DOI: 10.1007/s11172-012-0217-0
Authors Shklyaev Yu.V. 1 , Smolyak A.A. 1 , Firgang S.I. 2 , Konyushkin L.D. 2
Affiliations
1 Institute of Technical Chemistry, Ural Branch of the Russian Academy of Sciences, Perm, Russian Federation
2 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: A number of dihydroisoquinolines were synthesized by the reaction of apiol, a natural allylbenzene, with nitriles. When methyl thiocyanate was used as the nitrile component, the formation of 2-azaspiro[4.5]deca-1,6,9-trien-8-one derivatives, the spiroheterocyclization product, was also observed.
Cite: Shklyaev Y.V. , Smolyak A.A. , Firgang S.I. , Konyushkin L.D.
Polyalkoxybenzenes from plant material 6. Synthesis of 3-methyl-3,4-dihydroisoquinolines from apiol
Russian Chemical Bulletin. 2012. V.61. N8. P.1627-1630. DOI: 10.1007/s11172-012-0217-0 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000321772100020
≡ Scopus: 2-s2.0-84887345883
≡ OpenAlex: W2016396460
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