9-alkenylcarbazoles. 13. Trifluoroacetylation of trans- and cis-9-alkenylcarbazoles

N. V. Moskalev, V. D. Filimonov, E. E. Sirotkina

The Kizhner Research Center

Research output: Contribution to journal › Article › peer-review

Abstract

The trifluoroacetylation of 9-alkenylcarbazoles in pyridine takes place regio- and stereospecifically with the formation of the Β-trifluoroacetyl derivatives. The cis isomers are inert to trifluoroacetic anhydride.

Original language	English
Pages (from-to)	877-879
Number of pages	3
Journal	Chemistry of Heterocyclic Compounds
Volume	24
Issue number	8
DOIs	https://doi.org/10.1007/BF00479341
Publication status	Published - Aug 1988

ASJC Scopus subject areas

Organic Chemistry

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title = "9-alkenylcarbazoles. 13. Trifluoroacetylation of trans- and cis-9-alkenylcarbazoles",

abstract = "The trifluoroacetylation of 9-alkenylcarbazoles in pyridine takes place regio- and stereospecifically with the formation of the Β-trifluoroacetyl derivatives. The cis isomers are inert to trifluoroacetic anhydride.",

author = "Moskalev, {N. V.} and Filimonov, {V. D.} and Sirotkina, {E. E.}",

year = "1988",

month = aug,

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language = "English",

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journal = "Chemistry of Heterocyclic Compounds",

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AU - Filimonov, V. D.

AU - Sirotkina, E. E.

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AB - The trifluoroacetylation of 9-alkenylcarbazoles in pyridine takes place regio- and stereospecifically with the formation of the Β-trifluoroacetyl derivatives. The cis isomers are inert to trifluoroacetic anhydride.

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