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. Author manuscript; available in PMC: 2018 Sep 13.
Published in final edited form as: Nat Catal. 2018;1:673–679. doi: 10.1038/s41929-018-0123-4

Figure 3: C–H Functionalization with dienes and aldehydes.

Figure 3:

Reactions were performed on 0.2 mmol scale and proceeded with >98:2 dr unless otherwise noted, and isolated yields of product after purification by chromatography are reported. See Supplementary Methods for experimental details. a. 1a = [0.4 M]. b. 20% of the minor regioisomer was observed by NMR analysis. c. 1a = [1.0 M]. d. Isolated yield of major diastereomer, crude dr 92:8. e. Benzamide 1a (2.0 equiv), diene 2ar (1.0 equiv), and benzyloxyacetaldehyde (3.0 equiv).