Studies on the selective intramolecular biaryl coupling reaction of 2-triflyloxy-6-halobenzanilides using a palladium reagent

Takashi Harayama; Hiroko Toko; Kyoko Kubota; Hiromi Nishioka; Hitoshi Abe; Yasuo Takeuchi

doi:10.3987/COM-01-S(M)5

Studies on the selective intramolecular biaryl coupling reaction of 2-triflyloxy-6-halobenzanilides using a palladium reagent

Takashi Harayama, Hiroko Toko, Kyoko Kubota, Hiromi Nishioka, Hitoshi Abe, Yasuo Takeuchi

Research output: Contribution to journal › Article

7 Citations (Scopus)

Abstract

The aryl-aryl coupling reaction of 2-triflyloxy-6-halobenzanilides using a palladium reagent under several reaction conditions was examined. The 6-iodo compound gave triflyloxyphenanthridone selectively in excellent yield under the conditions for the ordinary Heck reaction.

Original language	English
Pages (from-to)	175-181
Number of pages	7
Journal	Heterocycles
Volume	58
DOIs	https://doi.org/10.3987/COM-01-S(M)5
Publication status	Published - Nov 22 2002

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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Harayama, T., Toko, H., Kubota, K., Nishioka, H., Abe, H., & Takeuchi, Y. (2002). Studies on the selective intramolecular biaryl coupling reaction of 2-triflyloxy-6-halobenzanilides using a palladium reagent. Heterocycles, 58, 175-181. https://doi.org/10.3987/COM-01-S(M)5

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abstract = "The aryl-aryl coupling reaction of 2-triflyloxy-6-halobenzanilides using a palladium reagent under several reaction conditions was examined. The 6-iodo compound gave triflyloxyphenanthridone selectively in excellent yield under the conditions for the ordinary Heck reaction.",

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AU - Abe, Hitoshi

AU - Takeuchi, Yasuo

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