Synfacts 2008(1): 0081-0081  
DOI: 10.1055/s-2007-991438
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart · New York

Alkoxide-Directed Iodine-Magnesium Exchange at sp3 Centers

Contributor(s): Paul Knochel, Tobias Thaler
F. F. Fleming*, S. Gudipati, V. A. Vu, R. J. Mycka, P. Knochel
Duquesne University, Pittsburgh, USA and Ludwig-Maximilians-Universität, München, Germany
Further Information

Publication History

Publication Date:
18 December 2007 (online)

Significance

The halogen-magnesium exchange is a well-established method for the preparation of sp2-hybridized Grignard reagents. The synthesis of sp3-hybridized Grignard reagents via halogen-magnesium exchange processes, however, is difficult and only comparatively few examples have been reported so far. In this article, a novel synthetic approach is presented in which iodine-magnesium exchange on sp3-carbon centers is achieved by the intramolecular directing effect of neighboring alkoxide groups. The exchange can thus proceed rapidly at -78 °C giving access to novel cyclic Grignard reagents.