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. Author manuscript; available in PMC: 2014 Mar 27.
Published in final edited form as: J Am Chem Soc. 2013 Mar 15;135(12):4652–4655. doi: 10.1021/ja400350c

Table 2.

Transannulation of 1-Mesyl-1,2,3-triazoles with Isocyanatesa

graphic file with name nihms-457195-t0005.jpg

entry product yield,
%b
entry product yield,
%b
entry product yield,
%b
1 graphic file with name nihms-457195-t0006.jpg 2b 95 7 graphic file with name nihms-457195-t0007.jpg 2h 83 13 graphic file with name nihms-457195-t0008.jpg 2n 97
2 graphic file with name nihms-457195-t0009.jpg 2c 94 8 graphic file with name nihms-457195-t0010.jpg 2i 53 14 graphic file with name nihms-457195-t0011.jpg 2o 82
3 graphic file with name nihms-457195-t0012.jpg 2d 94 9 graphic file with name nihms-457195-t0013.jpg 2j 89 15 graphic file with name nihms-457195-t0014.jpg 2p 95
4 graphic file with name nihms-457195-t0015.jpg 2e 94 10 graphic file with name nihms-457195-t0016.jpg 2k 92 16 graphic file with name nihms-457195-t0017.jpg 2q 93
5 graphic file with name nihms-457195-t0018.jpg 2f 80 11 graphic file with name nihms-457195-t0019.jpg 2l 69 17 graphic file with name nihms-457195-t0020.jpg 2r 90
6 graphic file with name nihms-457195-t0021.jpg 2g 85 12 graphic file with name nihms-457195-t0022.jpg 2m 85 18 graphic file with name nihms-457195-t0023.jpg 2s 92
a

Procedure: triazole 1 (1.0 mmol), isocyanate (1.2 mmol), Rh2(S-NTTL)4 (0.005 mmol) were stirred in 5 mL of dry chloroform at room temperature for 1-6 hours.

b

Isolated yield.