Highly Functionalized Organomagnesium Reagents Prepared through Halogen–Metal Exchange

Paul Knochel(Ludwig-Maximilians-Universität München), Wolfgang Döhle(Ludwig-Maximilians-Universität München), Nina Gommermann(Ludwig-Maximilians-Universität München), Florian F. Kneisel(Ludwig-Maximilians-Universität München), Felix Kopp(Ludwig-Maximilians-Universität München), Tobias J. Korn(Ludwig-Maximilians-Universität München), Ioannis Sapountzis(Ludwig-Maximilians-Universität München), Viet Anh Vu(Ludwig-Maximilians-Universität München)
Angewandte Chemie International Edition
September 17, 2003
Cited by 770

Abstract

Organomagnesium reagents occupy a central position in synthetic organic and organometallic chemistry. Recently, the halogen-magnesium exchange has considerably extended the range of functionalized Grignard reagents available for synthetic purposes. Functional groups such as esters, nitriles, iodides, imines, or even nitro groups can be present in a wide range of aromatic and heterocyclic organomagnesium reagents. Also various highly functionalized alkenyl magnesium species can be prepared. These recent developments as well as new applications of organomagnesium reagents in cross-coupling reactions and amination reactions will be covered in this Review.


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