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 › peer-review

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

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.",

author = "Takashi Harayama and Hiroko Toko and Kyoko Kubota and Hiromi Nishioka and Hitoshi Abe and Yasuo Takeuchi",

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AU - Harayama, Takashi

AU - Toko, Hiroko

AU - Kubota, Kyoko

AU - Nishioka, Hiromi

AU - Abe, Hitoshi

AU - Takeuchi, Yasuo

PY - 2002/11/22

Y1 - 2002/11/22

N2 - 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.

AB - 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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ER -

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

Abstract

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