Skip to main content
. 2018 Nov 26;10(4):994–999. doi: 10.1039/c8sc04437f

Table 2. Substrate scope of substituted aryl halides and triflates a .

graphic file with name c8sc04437f-u3.jpg
graphic file with name c8sc04437f-u4.jpg

aIsolated yields.

bReaction conditions for aryl bromides 1a–1s and aryl chloride 5a: 1 or 5, 0.40 mmol (0.027 M); 2 (5 mol%); L5 (5 mol%); 80 °C.

cReaction conditions for aryl triflates 4a, 4h, 4r, and 4s and aryl chlorides 5t–5v: 4 or 5, 0.40 mmol (0.027 M); 2 (15 mol%); L5 (15 mol%); 100 °C.

d 1H NMR yield.

e Si–Me4-DHP (1.1 equiv.) was used.