Volume 125, Issue 8 pp. 2263-2267
Zuschrift

A Cationic High-Valent Cp*CoIII Complex for the Catalytic Generation of Nucleophilic Organometallic Species: Directed CH Bond Activation

Tatsuhiko Yoshino

Tatsuhiko Yoshino

Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan) http://www.f.u-tokyo.ac.jp/∼kanai/e_index.html

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Hideya Ikemoto

Hideya Ikemoto

Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan) http://www.f.u-tokyo.ac.jp/∼kanai/e_index.html

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Dr. Shigeki Matsunaga

Corresponding Author

Dr. Shigeki Matsunaga

Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan) http://www.f.u-tokyo.ac.jp/∼kanai/e_index.html

Japan Science and Technology Agency, ACT-C, Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan)

Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan) http://www.f.u-tokyo.ac.jp/∼kanai/e_index.html===Search for more papers by this author
Prof. Dr. Motomu Kanai

Corresponding Author

Prof. Dr. Motomu Kanai

Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan) http://www.f.u-tokyo.ac.jp/∼kanai/e_index.html

Japan Science and Technology Agency, ERATO, Kanai Life Science Catalysis Project, Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan)

Graduate School of Pharmaceutical Sciences, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan) http://www.f.u-tokyo.ac.jp/∼kanai/e_index.html===Search for more papers by this author
First published: 16 January 2013
Citations: 147

This research was supported in part by the ERATO program of JST (M.K.), a Grant-in-Aid for Scientific Research on Innovative Areas (“Molecular Activation Directed toward Straightforward Synthesis”) from MEXT (S.M.), the ACT-C program of JST (S.M.), and the Naito Foundation. T.Y. thanks the JSPS for fellowships. Cp*=pentamethylcyclopentadienyl.

Graphical Abstract

Aktiv ohne Aktivierung: In einem preiswerten und atomökonomischen Ansatz der C-H-Funktionalisierung wird ein kationischer Cobalt(III)-Komplex verwendet, um nucleophile metallorganische Spezies in situ ohne Zusatz aktivierender Reagentien herzustellen (siehe Schema). Aryl-C-H-Bindungen addieren effizient an polare Elektrophile, einschließlich α,β-ungesättigter N-Acylpyrrole als β-substituierte Ester- und Amid-Surrogate.

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