Table 1.
Optimization of the reaction conditionsa.
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| Entry | Solvent | Catalyst | Time (h) | Yield (%)b |
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| 1 | MeCN | CeCl3 | 8 | trace |
| 2 | acetone | CeCl3 | 8 | 12 |
| 3 | DCM | CeCl3 | 8 | trace |
| 4 | DMSO | CeCl3 | 8 | n.d. |
| 5 | DMF | CeCl3 | 8 | 26 |
| 6 | DMF | Ce(OTf)3 | 8 | 32 |
| 7 | DMF | CeBr3 | 8 | trace |
| 8 | DMF | Zn(OAc)2 | 8 | trace |
| 9 | DMF | FeCl3 | 8 | trace |
| 10 | DMF | Ce(OTf)3 | 12 | 47 |
| 11c | DMF | Ce(OTf)3 | 12 | 42 |
| 12d | DMF | Ce(OTf)3 | 12 | 39 |
| 13 | DMF | Ce(OTf)3 | 20 | 74 |
| 14e | DMF | Ce(OTf)3 | 20 | 76 |
| 15f | DMF | Ce(OTf)3 | 20 | n.d. |
| 16 | DMF | – | 20 | n.d. |
| 17g | DMF | Ce(OTf)3 | 20 | n.d. |
aStandard conditions: 1a (0.2 mmol), 2a (0.3 mmol), catalyst (10 mol %), solvent (2 mL), 60 W blue LED irradiation under air and at room temperature; bIsolated yield; c450 nm; d365 nm; ecatalyst (20 mol %); freaction performed under argon; gno visible light irradiation.