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. Author manuscript; available in PMC: 2016 Jul 27.
Published in final edited form as: Angew Chem Int Ed Engl. 2015 Jun 12;54(31):9047–9051. doi: 10.1002/anie.201503297

Table 3.

Alkyl–alkyl cross-couplings of fluorinated secondary electrophiles: scope with respect to the perfluoroalkyl group.[a]

graphic file with name nihms711211u4.jpg
entry alkyl alkyl yield (%)[b]
1 n-C3F7 graphic file with name nihms711211t10.jpg 65
2 n-C3F7 graphic file with name nihms711211t11.jpg 54
3 n-C3F7 graphic file with name nihms711211t12.jpg 51
4 n-C3F7 graphic file with name nihms711211t13.jpg 69
5 n-C4F9 graphic file with name nihms711211t14.jpg 67
6 n-C4F9 graphic file with name nihms711211t15.jpg 54
7 n-C4F9 graphic file with name nihms711211t16.jpg 69
8 n-C9F19 graphic file with name nihms711211t17.jpg 66
[a]

All data are the average of two experiments.

[b]

Yield of purified product.