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. Author manuscript; available in PMC: 2016 Feb 4.
Published in final edited form as: J Am Chem Soc. 2015 Jan 15;137(4):1408–1411. doi: 10.1021/ja512306a

Table 3. Substrate scope with different aminesa.

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a

All yields are isolated yields.

b

4% of ortho-C–H vinylation product and 3% of sequential C–H/C–C activation product were observed.

c

6% of ortho-C–H vinylation product was observed.

d

2.0 equiv of alkyne 2a was used.

e

The reaction conversion was 83%, determined by crude 1H NMR.