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. Author manuscript; available in PMC: 2021 Feb 24.
Published in final edited form as: Nature. 2020 Apr 8;581(7809):415–420. doi: 10.1038/s41586-020-2213-0

Figure 2. Scope of the amine component in carbonyl alkylative amination.

Figure 2

a. Optimal reaction conditions. b. Scope of amine component. aNo TBSOTf used bTMSOTf used instead of TBSOTf. cAmine’HCl salt used. TMS: trimethylsilyl; Tf: trifluoromethanesulfonyl; Cy: cyclohexyl.