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. 2023 Jun 5;88(13):7901–7917. doi: 10.1021/acs.joc.2c02355

Table 2. Scope of the Reaction of 3a with Different Aryl Boronic Acids 4a,b,c.

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a

Reaction conditions: 3a (0.134 mmol), 4 (0.16 mmol), K2CO3 (0.27 mmol), Pd(PPh3)4 (6.7 μmol), DME (1 mL), 110 °C, 24 h.

b

Isolated yields.

c

Numbers in parentheses indicate estimated yields (in reference to the starting material) according to 31P NMR.

d

For fractions that, after purification, were contaminated with up to 5–7% of Ph3P(O), the yields of products were calculated according to 1H NMR.