Organocalcium-mediated nucleophilic alkylation of benzene

Author:

Wilson Andrew S. S.1ORCID,Hill Michael S.1ORCID,Mahon Mary F.1,Dinoi Chiara2ORCID,Maron Laurent2ORCID

Affiliation:

1. Department of Chemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK.

2. Université de Toulouse et CNRS, Institut National des Sciences Appliquées, Université Toulouse III–Paul Sabatier, UMR 5215, LPCNO, 135 Avenue de Rangueil, F-31077 Toulouse, France.

Abstract

Calcium can breach benzene's defenses Calcium plays a major, multifaceted role in biology and mineralogy. In organic chemistry, though, it is largely overlooked and overshadowed by the carbon compounds of its cousins lithium and magnesium. Wilson et al. now report that the element was just biding its time: Several organocalcium compounds that they prepared can alkylate benzene by displacing a hydride, with no need for a more conventionally reactive leaving group such as chloride (see the Perspective by Mulvey). This surprising, previously elusive reaction attests to the unusual nucleophilicity of the carbons bound to calcium. Science , this issue p. 1168 ; see also p. 1132

Funder

Engineering and Physical Sciences Research Council

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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