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Terpenic methyl ketones derived from limonene, (+)-3-carene, and alpha-pinene in Fischer's indole synthesis. Full article

Journal Heterocyclic Communications
ISSN: 0793-0283
Output data Year: 2000, Volume: 6, Number: 1, Pages: 73-80 Pages count : 8
Authors Burchak Olga Ν. 1 , Chibiryaev Andrey M. 2 , Tkachev Alexey V. 2
Affiliations
1 Department of Natural Sciences Novosibirsk State University
2 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry of Siberian Branch of Russian Academy of Sciences

Abstract: Methyl ketones derived from monoterpene hydrocarbons limonene, a-pinene, and (+)-3-carene are converted into a new terpendoles in Fischer's indole synthesis. Regioselectivity of indole formation depend on the structural features of starting ketones but not on the reaction conditions.
Cite: Burchak O.Ν. , Chibiryaev A.M. , Tkachev A.V.
Terpenic methyl ketones derived from limonene, (+)-3-carene, and alpha-pinene in Fischer's indole synthesis.
Heterocyclic Communications. 2000. V.6. N1. P.73-80. WOS РИНЦ
Identifiers:
Web of science: WOS:000085709500014
Elibrary: 13337661
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