Answers are grounded in this paper and cite their sources.
The copper-catalyzed conjugate addition of Grignard reagents to 3-substituted cyclic enones allows the formation of all-carbon chiral quaternary centers. We demonstrate in this article that N-heterocyclic carbenes act as efficient chiral ligands for this transformation. High enantioselectivities (up to 96% ee) could be obtained for a variety of substrates.
No takes yet. Share an insight, caveat, or question.
Kehrli et al. (2010) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: