Answers are grounded in this paper and cite their sources.
Asymmetric catalytic C–C coupling reactions via C–H bond activation are currently among the most attractive and powerful tools in synthetic organic chemistry. In the past few decades, a variety of catalytic asymmetric C–C coupling reactions via C–H bond activation have been reported. Compared with traditional asymmetric C–C bond formation reactions, C–H activation/C–C coupling strategies have more advantages in terms of power and cost-effectiveness. In this review, after a short introduction of C–H activation/C–C coupling reactions, recent studies on C–H activation/C–C coupling reactions are reviewed, with an emphasis on enantioselective cross-dehydrogenative-coupling, C–H activation/olefin coupling reactions, hydroacylation of aldehydes via C–H activation, as well as C–H activation/R–X(M) coupling reactions.
No takes yet. Share an insight, caveat, or question.
Yang et al. (2012) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: