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. Author manuscript; available in PMC: 2018 Sep 6.
Published in final edited form as: J Am Chem Soc. 2017 Aug 22;139(35):12299–12309. doi: 10.1021/jacs.7b06811

Figure 5.

Figure 5

Co-Catalyst Structure–Reactivity–Enantioselectivity Relationships. Enantiomeric excess reported for the formation of 4b under the conditions shown. Relative rate constants (krel) determined from the first-order rate constants for formation of 4a under the conditions in Scheme 1. Arb = 4-chlorophenyl. ArF = 3,5-bis(trifluoromethyl)phenyl.