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

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

Журнал

Heterocyclic Communications
ISSN: 0793-0283

Вых. Данные

Год: 2000, Том: 6, Номер: 1, Страницы: 73-80 Страниц : 8

Авторы

Burchak Olga Ν. ¹ , Chibiryaev Andrey M. ² , Tkachev Alexey V. ²

Организации

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

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.

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

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