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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 4.

Alkyl–alkyl cross-couplings to generate trifluoromethyl-substituted products: scope with respect to the nucleophile.[a]

graphic file with name nihms711211u5.jpg
entry alkyl yield (%)[b]
1 graphic file with name nihms711211t18.jpg 79
2 graphic file with name nihms711211t19.jpg 78
3 graphic file with name nihms711211t20.jpg 83
4 graphic file with name nihms711211t21.jpg 74
5 graphic file with name nihms711211t22.jpg 72
6 graphic file with name nihms711211t23.jpg 83
7 graphic file with name nihms711211t24.jpg 67
8 graphic file with name nihms711211t25.jpg 83
9 graphic file with name nihms711211t26.jpg 89
[a]

All data are the average of two experiments.

[b]

Yield of purified product.