Table 2. Catalyst structure–activity relationship studies a .
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Entry | Metal source | Ligand | Yield (3 + 4) | rr (3 : 4) | Yield 5 |
1 | — | — | <1% | — | <1% |
2 | CoBr2 | — | <1% | — | <1% |
3 | Co(DME)Br2 | — | <1% | — | <1% |
4 | — | i–PrPDI | <1% | — | <1% |
5 | CoBr2 | i–PrPDI | 81% | >50 : 1 | <1% |
6 | CoBr2 | MePDI | 58% | >50 : 1 | <1% |
7 | CoBr2 | PhPDI | 4% | — | <1% |
8 | CoBr2 | i–PrDAD | <1% | — | <1% |
9 | CoBr2 | i–PrIP | 2% | — | <1% |
10 | CoBr2 | Terpy | 4% | — | <1% |
11 | CoBr2 | t–BuPyBOX | <1% | — | <1% |
12 | CoBr2 | PhPyBOX | <1% | — | <1% |
13 | CoBr2 | PPh3 (12 mol%) | <1% | — | 0% |
14 | FeBr2 | i–PrPDI | 3% | — | <1% |
15 | NiBr2 | i–PrPDI | <1% | — | <1% |
aReaction conditions: 4-vinylcyclohexene (0.14 mmol), THF (1.0 mL), 24 h, 22 °C. Yields and ratios of regioisomers were determined by GC analysis against an internal standard.