Answers are grounded in this paper and cite their sources.
In the presence of a catalytic amount of a nickel salt, aryl tert-butyl sulfones react with aryl Grignard reagents to give biaryls. This reaction is used in conjunction with the powerful ortho-lithiation-directing ability of aryl tert-butyl sulfonyl groups to make unsymmetrical ortho-substituted biaryls. In certain cases, the substitution of an aryl alkylsulfonyl group by an organometallic reagent is possible without a transition metal catalyst.
No takes yet. Share an insight, caveat, or question.
Clayden et al. (1995) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: