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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 2.

Cross-coupling of Allylbenzene with Aryl bromides.

entry product yield
(%)[a]
entry product yield
(%)[a]
1 graphic file with name nihms589670t2.jpg 91[b] 8 graphic file with name nihms589670t3.jpg 86[c]
2 graphic file with name nihms589670t4.jpg 88[b] 9 graphic file with name nihms589670t5.jpg 74[c]
3 graphic file with name nihms589670t6.jpg 97[b] 10 graphic file with name nihms589670t7.jpg 86[c,d]
4 graphic file with name nihms589670t8.jpg 81[b] 11 graphic file with name nihms589670t9.jpg 66[c,d]
5 graphic file with name nihms589670t10.jpg 86[c] 12 graphic file with name nihms589670t11.jpg 52[b]
6 graphic file with name nihms589670t12.jpg 85[c,d] 13 graphic file with name nihms589670t13.jpg 65[c,d]
7 graphic file with name nihms589670t14.jpg 83[c,e] 14 graphic file with name nihms589670t15.jpg 87[c,d]
[a]

Less than 4 % of the gamma products were detected by NMR and no Heck product was observed under our conditions.

[b]

24 h.

[c]

36 h.

[d]

6 eq. of base used.

[e]

Concentration is 0.3M