Skip to main content
. 2020 Jun 14;142(26):11382–11387. doi: 10.1021/jacs.0c05343

Table 2. Scope of the Bi-Catalyzed Oxidative Coupling of Arylboronic Acids and Sodium Triflatea.

graphic file with name ja0c05343_0006.jpg

graphic file with name ja0c05343_0007.jpg

a

Reaction conditions: 1 (0.3 mmol), NaOTf (0.33 mmol), 4c (0.03 mmol), [Cl2pyrF]BF4 (0.33 mmol), Na3PO4 (0.6 mmol), and 5 Å MS (120 mg) in CHCl3 at 60 °C for 16 h. Yields of isolated pure material.

b

Reaction performed at 90 °C with 2.0 equiv of NaF as base.

c

Yields determined by 19F NMR using 1-fluoro-4-nitrobenzene as internal standard.

d

Reactions performed at 0.025 mmol of the corresponding arylboronic acids.

e

Reaction performed at 90 °C with 4.0 equiv of Na3PO4 as base.