Volume 125, Issue 8 pp. 2273-2276
Zuschrift

Palladium-Catalyzed Intramolecular ipso-Friedel–Crafts Alkylation of Phenols and Indoles: Rearomatization-Assisted Oxidative Addition

Dr. Tetsuhiro Nemoto

Dr. Tetsuhiro Nemoto

Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675 (Japan)

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Zengduo Zhao

Zengduo Zhao

Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675 (Japan)

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Takuya Yokosaka

Takuya Yokosaka

Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675 (Japan)

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Yuta Suzuki

Yuta Suzuki

Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675 (Japan)

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Riliga Wu

Riliga Wu

Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675 (Japan)

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Prof. Dr. Yasumasa Hamada

Corresponding Author

Prof. Dr. Yasumasa Hamada

Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675 (Japan)

Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8675 (Japan)===Search for more papers by this author
First published: 15 January 2013
Citations: 43

This work was supported by Grant-in Aid for Scientific Resarch from the JSPS (Japan), the Research Foundation for Pharmaceutical Sciences, Chiba Univsersity, and the Inohana Foundation (Chiba University).

Graphical Abstract

Inspiroierend: Eine neuartige Synthese von Spirocyclen basierend auf einer Palladium-katalysierten intramolekularen ipso-Friedel-Crafts-Alkylierung von Phenolen (siehe Schema; dba=Dibenzylidenaceton) und Indolen wird beschrieben. Mechanistische Studien belegen, dass die Reaktion über eine präzedenzlose Rearomatisierungs-unterstützte oxidative Addition verläuft.

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