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. Author manuscript; available in PMC: 2015 Sep 15.
Published in final edited form as: Angew Chem Int Ed Engl. 2014 Jul 24;53(38):10209–10212. doi: 10.1002/anie.201404579

Table 2.

Reaction Scope with Respect to Arylamides [a]

graphic file with name nihms626761t2.jpg

Entry Ar Product Yield, %
1 C6H5 graphic file with name nihms626761t3.jpg 78
2 4-CF3C6H4 graphic file with name nihms626761t4.jpg 70
3 4-BrCC6H4 graphic file with name nihms626761t5.jpg 73
4 4-NO2C6H4 graphic file with name nihms626761t6.jpg 78
5 2-MeC6H4 graphic file with name nihms626761t7.jpg 86
6 3-IC6H4 graphic file with name nihms626761t8.jpg 84
7[b] 2-MeOC6H4 graphic file with name nihms626761t9.jpg 74
8[c] 2-furyl graphic file with name nihms626761t10.jpg 81
9[d] 2-thiophenyl graphic file with name nihms626761t11.jpg 86
[a]

Amide 0.5 mmol, CF3CH2OH 5 mL, air. Yields are isolated yields. Please see Supporting information for details.

[b]

Time: 18 h.

[c]

Time: 16 h.

[d]

Time: 20 h.