Oxidative C-H/C-H coupling of azine and indole/pyrrole nuclei: Palladium catalysis and synthesis of eudistomin U

Atsushi D. Yamaguchi; Debashis Mandal; Junichiro Yamaguchi; Kenichiro Itami

doi:10.1246/cl.2011.555

Oxidative C-H/C-H coupling of azine and indole/pyrrole nuclei: Palladium catalysis and synthesis of eudistomin U

Atsushi D. Yamaguchi, Debashis Mandal, Junichiro Yamaguchi, Kenichiro Itami

研究成果: Review article › 査読

112 被引用数 (Scopus)

抄録

We have developed a palladium-catalyzed C-H/C-H coupling reaction of indoles or pyrroles with azine N-oxides. The reaction proceeds selectively at the C3 position of indoles/pyrroles and the C2 position of azine N-oxides. Furthermore, we have accomplished the synthesis of marine indole alkaloid eudistomin U by utilizing this newly developed C-H/C-H coupling reaction.

本文言語	English
ページ（範囲）	555-557
ページ数	3
ジャーナル	Chemistry Letters
巻	40
号	6
DOI	https://doi.org/10.1246/cl.2011.555
出版ステータス	Published - 2011
外部発表	はい

ASJC Scopus subject areas

化学 (全般)

UN SDG

この成果は、次の持続可能な開発目標に貢献しています

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10.1246/cl.2011.555

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abstract = "We have developed a palladium-catalyzed C-H/C-H coupling reaction of indoles or pyrroles with azine N-oxides. The reaction proceeds selectively at the C3 position of indoles/pyrroles and the C2 position of azine N-oxides. Furthermore, we have accomplished the synthesis of marine indole alkaloid eudistomin U by utilizing this newly developed C-H/C-H coupling reaction.",

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journal = "Chemistry Letters",

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T2 - Palladium catalysis and synthesis of eudistomin U

AU - Yamaguchi, Atsushi D.

AU - Mandal, Debashis

AU - Yamaguchi, Junichiro

AU - Itami, Kenichiro

PY - 2011

Y1 - 2011

N2 - We have developed a palladium-catalyzed C-H/C-H coupling reaction of indoles or pyrroles with azine N-oxides. The reaction proceeds selectively at the C3 position of indoles/pyrroles and the C2 position of azine N-oxides. Furthermore, we have accomplished the synthesis of marine indole alkaloid eudistomin U by utilizing this newly developed C-H/C-H coupling reaction.

AB - We have developed a palladium-catalyzed C-H/C-H coupling reaction of indoles or pyrroles with azine N-oxides. The reaction proceeds selectively at the C3 position of indoles/pyrroles and the C2 position of azine N-oxides. Furthermore, we have accomplished the synthesis of marine indole alkaloid eudistomin U by utilizing this newly developed C-H/C-H coupling reaction.

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U2 - 10.1246/cl.2011.555

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JO - Chemistry Letters

JF - Chemistry Letters

IS - 6

ER -

Oxidative C-H/C-H coupling of azine and indole/pyrrole nuclei: Palladium catalysis and synthesis of eudistomin U

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ASJC Scopus subject areas

UN SDG

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