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. 2013 Nov 15;9:2476–2536. doi: 10.3762/bjoc.9.287

Table 5.

Pd-catalyzed C–H trifluoromethylation employing Umemoto’s sulfonium tetrafluoroborate salt [67].

graphic file with name Beilstein_J_Org_Chem-09-2476-i066.jpg

Product Yield (%)a Product Yield (%)a

graphic file with name Beilstein_J_Org_Chem-09-2476-i067.jpg 86 graphic file with name Beilstein_J_Org_Chem-09-2476-i068.jpg 0c
graphic file with name Beilstein_J_Org_Chem-09-2476-i069.jpg 82 graphic file with name Beilstein_J_Org_Chem-09-2476-i070.jpg 88
graphic file with name Beilstein_J_Org_Chem-09-2476-i071.jpg 2-Me
3-Me
4-Me
84
83
83
graphic file with name Beilstein_J_Org_Chem-09-2476-i072.jpg 75c
graphic file with name Beilstein_J_Org_Chem-09-2476-i073.jpg 2-OMe
3-OMe
4-OMe
78
54b
68
graphic file with name Beilstein_J_Org_Chem-09-2476-i074.jpg 58c
graphic file with name Beilstein_J_Org_Chem-09-2476-i075.jpg 2-Cl
3-Cl
4-Cl
55c
75c
72c
graphic file with name Beilstein_J_Org_Chem-09-2476-i076.jpg 62c
graphic file with name Beilstein_J_Org_Chem-09-2476-i077.jpg 78b graphic file with name Beilstein_J_Org_Chem-09-2476-i078.jpg 53c
graphic file with name Beilstein_J_Org_Chem-09-2476-i079.jpg 87b graphic file with name Beilstein_J_Org_Chem-09-2476-i080.jpg 74
graphic file with name Beilstein_J_Org_Chem-09-2476-i081.jpg 88

aYields for isolated compounds. b15 mol % of Pd(OAc)2 were used. c20 mol % of Pd(OAc)2 were used.