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. Author manuscript; available in PMC: 2025 May 3.
Published in final edited form as: ACS Catal. 2024 Apr 11;14(9):6404–6412. doi: 10.1021/acscatal.4c00648

Table 5.

Exploring product selectivity in Ni-catalyzed arylation of 1,3-dichlorobenzenea,b

graphic file with name nihms-2000308-t0015.jpg
entry PR3 solvent ArB(OH)2 (equiv) 2s (%) 3s (%) 2s : 3s
1 PPh2Me MeCN 1.1 63 16 4 : 1
2 THF 1.1 50 24 2 : 1
3 PCy3 MeCN 1.1 6 36 1 : 6
4 THF 1.1 6 48 1 : 8
5 MeCN 2.2 9 63 1 : 7
6 THF 2.2 7 90 1 : 13
a

Reactions performed on 0.1 mmol scale (c = 0.2 M).

b

Yields determined by 19F NMR using trifluorotoluene as internal standard.