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. Author manuscript; available in PMC: 2015 Jun 1.
Published in final edited form as: Chem Sci. 2014 Mar 28;5(6):2422–2427. doi: 10.1039/C4SC00697F

Table 3.

[Co(P1)]-Catalyzed Amination of p-Anisaldehyde (1b) with Various Aryl Azidesa,b

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a

All reactions were carried out in PhCl using 3 mol % of [Co(P1)] as catalyst with 1.0 equiv. of aldehyde (0.2 M) and 1.2 equiv. of azide for 24 h at 80 °C.

b

Isolated yields.

c

At 100 °C.

d

The yield was based on 1H NMR.