Highly efficient construction of benzene ring in carbazoles by palladium-catalyzed endo-mode oxidative cyclization of 3-(3'-alkenyl)indoles.

doi:10.1021/OL060039U

Paper

DOI: 10.1021/OL060039U

Highly efficient construction of benzene ring in carbazoles by palladium-catalyzed endo-mode oxidative cyclization of 3-(3'-alkenyl)indoles.

Published Mar 7, 2006 · A. Kong, Xiuling Han, Xiyan Lu

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Abstract

[reaction: see text] A highly efficient construction of the benzene ring in carbazoles by palladium-catalyzed endo-mode oxidative cyclization of 3-(3'-alkenyl)indoles was developed. The reaction utilizes benzoquinone as the stoichiometric oxidant and is conducted under mild conditions.

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Study Snapshot

This method efficiently constructs benzene rings in carbazoles using mild conditions and benzoquinone as the stoichiometric oxidant, offering potential applications in organic synthesis and catalysis.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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