. 2014 Mar 12;136(14):5257–5260. doi: 10.1021/ja501621q

Table 3. Decarboxylative Arylation: Aromatic Scope^a^,^b.

graphic file with name ja-2014-01621q_0006.jpg

graphic file with name ja-2014-01621q_0007.jpg

Cited yields are of material isolated by column chromatography. See Supporting Information for experimental details.

Regiomeric ratios (rr) determined by ¹H NMR (major isomer is shown).

1.3:1 rr.

4:1 chemoselectivity for addition to ipso-CN vs SO₂Ph position.

Table 3. Decarboxylative Arylation: Aromatic Scopea,b.