Cu-MOF catalyzed synthesis of benzoxanthenone derivatives (4a–j)a.
| Entry | Aldehyde | Product | Product structure | Time (min) | Yieldb (%) | Mpc (°C) |
|---|---|---|---|---|---|---|
| 1 |
|
4a |
|
25 | 90 | 150–151c |
| 2 |
|
4b |
|
40 | 85 | 174–176c |
| 3 |
|
4c |
|
60 | 80 | 205–206c |
| 4 |
|
4d |
|
60 | 85 | 202–204c |
| 5 |
|
4e |
|
50 | 80 | 193–194c |
| 6 |
|
4f |
|
20 | 84 | 184–186c |
| 7 |
|
4g |
|
60 | 88 | 205–206c |
| 8 |
|
4h |
|
50 | 92 | 180–182 |
| 9 |
|
4i |
|
60 | 90 | 185–187 |
| 10 |
|
4j |
|
60 | 90 | 170–172 |
Conditions: 1 (1 mmol), 2 (1 mmol), 3 (1 mmol), Cu-MOF (0.05 g), stirring at 60–70 °C.
Product yield.
Melting points of known cpds match with literature values.35,36