Cooperative catalysis enables the direct enantioselective α-allylation of linear prochiral esters with 2-substituted allyl electrophiles. Critical to the successful development of the method was the recognition that metal-centered reactivity and the source of enantiocontrol are independent. This feature is unique to simultaneous catalysis events and permits logical tuning of the supporting ligands without compromising enantioselectivity.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038818 | PMC |
http://dx.doi.org/10.1002/anie.201803277 | DOI Listing |
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