Skip to main content
. 2019 Apr 17;10(20):5275–5282. doi: 10.1039/c9sc00554d

Table 2. Substrate scope of (hetero)arylboronic acid partners a .

graphic file with name c9sc00554d-u3.jpg
graphic file with name c9sc00554d-u4.jpg

aGeneral conditions: (hetero)arylboronic acid (0.6 mmol), CF3CH2I (0.4 mmol), base (0.8 mmol), 2.5 mol% precatalyst loading, DME (2.0 mL), 80 °C.

bIsolated yield.

cYield determined by 19F NMR spectroscopy using PhCF3 as an internal standard due to the volatility of naphthalene products. Data in parentheses refer to yields of isolated products.

d5.0 mol% precatalyst loading.