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. Author manuscript; available in PMC: 2020 Jul 7.
Published in final edited form as: Chem Commun (Camb). 2019 Jun 14;55(53):7599–7602. doi: 10.1039/c9cc04265b

Table 2.

Aryl radical scopea,b

graphic file with name nihms-1575091-t0007.jpg
a

All values indicate the yield of the isolated product.

b

General reaction conditions: aryl halide (2.0 equiv, 1.0 mmol), alkene (1.0 equiv, 0.50 mmol), Cl-4CzIPN (5 mol %, 0.025 mmol), TMS3SiOH (1.5 equiv, 0.75 mmol), Na2CO3 (4 equiv, 2.0 mmol), DMSO (0.1 M), 18 h, irradiating with blue LEDs (30 W). See the Supporting Information for details.

c

Isolated yield on 2.5 mmol scale; reaction run for 5 d.

d

Isolated on 1.0 mmol scale.

e

Isolated yield on 0.3 mmol scale.

f

Conducted using 10 mol % Cl-4CzIPN.

g

Reaction run for 2 d.

h

Conducted using 1 equiv Ar–X. hIsolated with <5% impurity of alkene.

i

Isolated as a 7.6:1 mixture of Br:I arene.