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. Author manuscript; available in PMC: 2015 Sep 15.
Published in final edited form as: Adv Synth Catal. 2014 Sep 10;356(13):2831–2837. doi: 10.1002/adsc.201400742

Table 5.

[3+2] Annulation of various aryl amines.[a]

graphic file with name nihms-640061-t0018.jpg

Entry Substrate Time (h)[b] Product Yield (%)[c]
1 graphic file with name nihms-640061-t0019.jpg 48 graphic file with name nihms-640061-t0020.jpg 8a 0[d]
2 graphic file with name nihms-640061-t0021.jpg 16 graphic file with name nihms-640061-t0022.jpg 8b 13
3 graphic file with name nihms-640061-t0023.jpg 21 graphic file with name nihms-640061-t0024.jpg 8c 48
4 graphic file with name nihms-640061-t0025.jpg 18 graphic file with name nihms-640061-t0026.jpg 8d 47
[a]

A solution of 1 (0.2 mmol), Ru(bpz)3(PF6)2 (2 mol%), and 2a (5 equiv.) in 2 mL CH3NO2 was degassed via freeze-pump-thaw cycles. The resulting solution was irradiated using an 18 W white LED.

[b]

Monitored by TLC.

[c]

Isolated yields.

[d]

Determined using GC-MS.