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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 2.

Alkyl–alkyl cross-couplings of fluorinated secondary electrophiles: scope.[a]

graphic file with name nihms711211u3.jpg
entry alkyl alkyl yield (%)[b]
1 CH2CH2Ph graphic file with name nihms711211t1.jpg 74
2 CH2CH2Ph graphic file with name nihms711211t2.jpg 55
3 CH2CH2Ph graphic file with name nihms711211t3.jpg 61
4 CH2CH2Ph graphic file with name nihms711211t4.jpg 59
5 CH2CH2Ph graphic file with name nihms711211t5.jpg 66
6 CH2CH2Ph graphic file with name nihms711211t6.jpg 70
7 CH2CH2Ph graphic file with name nihms711211t7.jpg 77
8 graphic file with name nihms711211t8.jpg graphic file with name nihms711211t9.jpg 64
[a]

All data are the average of two experiments.

[b]

Yield of purified product.