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. Author manuscript; available in PMC: 2014 Jun 1.
Published in final edited form as: Chem Sci. 2013 Mar 18;4(6):2374–2379. doi: 10.1039/C3SC50184A

Table 3.

Various aryl halides in C-3 arylationa

graphic file with name nihms464533f5.jpg
a

Reaction conditions: Pd(OAc)2 (10 mol %), Phen (10 mol %), Cs2CO3 (1.0 equiv), indazole (0.25 mmol), ArX (0.5 mmol) in toluene (1 mL) for 48 h and then isolated yield was obtained.

b

3-Bromopyridine (1.0 mmol) was used.