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. Author manuscript; available in PMC: 2020 Jul 6.
Published in final edited form as: Angew Chem Int Ed Engl. 2019 Oct 8;58(47):17068–17073. doi: 10.1002/anie.201910304

Table 4.

Scope of Alkene Aryl/Alkenylsilylation.[a]

graphic file with name nihms-1603231-t0005.jpg
[a]

Reaction conditions: 1a, 1c, 1z (0.1 mmol), 2a–d, 2g, 2i (1.5 equiv), 3b (3 equiv), Pd2dba3 (5 mol%), L (10 mol%), i-Pr2NEt (2 equiv), 4Å MS (30 mg), 100 °C, N2, 38–44 h. All the yields refer to the isolated yields.