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. Author manuscript; available in PMC: 2016 Feb 16.
Published in final edited form as: Angew Chem Int Ed Engl. 2015 Jan 7;54(8):2361–2365. doi: 10.1002/anie.201410039

Table 1.

Fluorination and Ligands Enable Regioselective Allylation Reactions.[a]

graphic file with name nihms664954t1.jpg
[a]

Catalyst System A: substrate (1.0 equiv), Pd(OAc)2 (3.0 mol%), t-BuBrettPhos (6.0 mol%), 1,4-dioxane (0.50 M), 60 °C, 20 h; Catalyst System B: substrate (1.0 equiv), Pd(OAc)2 (2.5 mol%), PhXPhos (5.0 mol%), 1,4-dioxane (0.10 M), 90 °C, 20 h. For fluorinated products, yields and selectivities were determined by 19F NMR using PhCF3 or PhF as an internal standard, respectively. For non-fluorinated products, yields and selectivities were determined by 1H NMR using CH2Br2 as an internal standard.