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Communication

Iron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents

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Masaharu Nakamura,*^† Keiko Matsuo, Shingo Ito, and Eiichi Nakamura*;

Department of Chemistry, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

J. Am. Chem. Soc., 2004, 126 (12), pp 3686–3687

DOI: 10.1021/ja049744t

Publication Date (Web): March 4, 2004

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

†

PRESTO, Japan Science and Technology Agency (JST).

, masaharu@chem.s.u-tokyo.ac.jp, ; , nakamura@chem.s.u-tokyo.ac.jp

Abstract

An iron-catalyzed cross-coupling reaction of a primary or secondary alkyl halide with an aryl Grignard reagent proceeds under mild conditions to give the corresponding coupling product in quantitative yield.

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Published In Issue March 31, 2004
Received January 15, 2004

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Communication

Iron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents

Abstract

Tools

SciFinder Links

History

Recommend & Share

Related Content

Iron-Catalyzed Cross-Coupling Reactions

Iron-Catalyzed Reactions in Organic Synthesis

Iron-Catalyzed Selective Biaryl Coupling: Remarkable Suppression of Homocoupling by the Fluoride Anion

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