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. Author manuscript; available in PMC: 2015 Apr 1.
Published in final edited form as: Angew Chem Int Ed Engl. 2014 Feb 26;53(14):3693–3697. doi: 10.1002/anie.201309084

Table 3.

Cross-coupling of Allylbenzenes with Aryl bromides.

entry product yield (%)[a] entry product yield (%)[a]
1 graphic file with name nihms589670t16.jpg 88 7 graphic file with name nihms589670t17.jpg 82
2 graphic file with name nihms589670t18.jpg 81 8 graphic file with name nihms589670t19.jpg 60[b]
3 graphic file with name nihms589670t20.jpg 72 9 graphic file with name nihms589670t21.jpg 64
4 graphic file with name nihms589670t22.jpg 66[b] 10 graphic file with name nihms589670t23.jpg 66
5 graphic file with name nihms589670t24.jpg 80[b] 11 graphic file with name nihms589670t25.jpg 51[c]
6 graphic file with name nihms589670t26.jpg 91
[a]

Reaction ran for 36 h.

[b]

6 eq. of base used.

[c]

5 eq. of thiophene allyl and 3 eq. of base used; obtained product along with 12 % of linear products.