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. 2016 Apr 26;7(8):5384–5389. doi: 10.1039/c6sc01148a

Table 1. Scope of aryl carbamic chlorides with different substituents a .

graphic file with name c6sc01148a-u1.jpg

aReaction conditions: 1a (0.2 mmol), 2 (0.4 mmol), Pd(OAc)2 (0.02 mmol), PPh3 (0.04 mmol), NBE (0.2 mmol), and Cs2CO3 (0.8 mmol) in DCE (2 mL) at 95 °C for 6 h.

bRegioselectivity ratio (the major isomer is substituted at the 3-position as drawn).

cThe reaction was conducted in toluene.