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. Author manuscript; available in PMC: 2012 Mar 4.
Published in final edited form as: Org Lett. 2011 Feb 3;13(5):1076–1079. doi: 10.1021/ol103121r

Table 3.

Substrate Scope for 1,1-Arylacetoxylation

graphic file with name nihms270350u4.jpg
Entry substrate product isolated (crude) yielda
1 graphic file with name nihms270350t1.jpg graphic file with name nihms270350t2.jpg
(4)
62% (64%)
2 graphic file with name nihms270350t3.jpg graphic file with name nihms270350t4.jpg
(5)
61% (62%)
3 graphic file with name nihms270350t5.jpg graphic file with name nihms270350t6.jpg
(6)
47% (54%)
4 graphic file with name nihms270350t7.jpg graphic file with name nihms270350t8.jpg
(7)
53% (61%)
5 graphic file with name nihms270350t9.jpg graphic file with name nihms270350t10.jpg
(8)
64% (67%)
6 graphic file with name nihms270350t11.jpg graphic file with name nihms270350t12.jpg
(9)
67% (72%)
7 graphic file with name nihms270350t13.jpg graphic file with name nihms270350t14.jpg
(10)
62% (62%)
8 graphic file with name nihms270350t15.jpg graphic file with name nihms270350t16.jpg
(11)
64% (71%)
9 graphic file with name nihms270350t17.jpg graphic file with name nihms270350t18.jpg
(12)
58% (69%)
a

Crude yields of products determined by 1H NMR spectroscopic analysis of crude reaction mixture. In most reactions 5–15% of the corresponding Heck product formation was observed along with <5% of the 1,1-arylchlorinated product.