Transition metal–catalyzed alkyl-alkyl bond formation: Another dimension in cross-coupling chemistry

Author:

Choi Junwon1ORCID,Fu Gregory C.2ORCID

Affiliation:

1. Department of Chemistry, Stanford University, Stanford, CA 94305, USA.

2. Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

Abstract

Stitching one alkyl group to another Chemical reactions such as Heck and Suzuki coupling facilitate access to an enormous range of relatively flat molecules. This geometrical constraint is associated with the comparative ease of linking together aryl and alkenyl carbons. Choi and Fu review recent developments in forming bonds between the more abundant alkyl carbon centers that underlie diverse molecules with complex three-dimensional structures. Nickel catalysis in particular has emerged as a powerful method to access individual mirror-image isomers selectively and thereby tune the biological properties of the targeted products. Science , this issue p. eaaf7230

Funder

National Institute of General Medical Sciences

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference63 articles.

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3. E. J. Corey X.-M. Cheng The Logic of Chemical Synthesis (Wiley 1995).

4. S. E. Denmark R. F. Sweis in Metal-Catalyzed Cross-Coupling Reactions A. de Meijere F. Diederich Eds. (Wiley-VCH 2004) pp. 163–216.

5. Synthesis of axially chiral biaryl compounds by asymmetric catalytic reactions with transition metals;Loxq P.;Coord. Chem. Rev.,2016

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