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. 2024 Jun 27;14(29):20454–20465. doi: 10.1039/d4ra03468f

Cu-MOF catalyzed synthesis of benzoxanthenone derivatives (4a–j)a.

Entry Aldehyde Product Product structure Time (min) Yieldb (%) Mpc (°C)
1 graphic file with name d4ra03468f-u4.jpg 4a graphic file with name d4ra03468f-u5.jpg 25 90 150–151c
2 graphic file with name d4ra03468f-u6.jpg 4b graphic file with name d4ra03468f-u7.jpg 40 85 174–176c
3 graphic file with name d4ra03468f-u8.jpg 4c graphic file with name d4ra03468f-u9.jpg 60 80 205–206c
4 graphic file with name d4ra03468f-u10.jpg 4d graphic file with name d4ra03468f-u11.jpg 60 85 202–204c
5 graphic file with name d4ra03468f-u12.jpg 4e graphic file with name d4ra03468f-u13.jpg 50 80 193–194c
6 graphic file with name d4ra03468f-u14.jpg 4f graphic file with name d4ra03468f-u15.jpg 20 84 184–186c
7 graphic file with name d4ra03468f-u16.jpg 4g graphic file with name d4ra03468f-u17.jpg 60 88 205–206c
8 graphic file with name d4ra03468f-u18.jpg 4h graphic file with name d4ra03468f-u19.jpg 50 92 180–182
9 graphic file with name d4ra03468f-u20.jpg 4i graphic file with name d4ra03468f-u21.jpg 60 90 185–187
10 graphic file with name d4ra03468f-u22.jpg 4j graphic file with name d4ra03468f-u23.jpg 60 90 170–172
a

Conditions: 1 (1 mmol), 2 (1 mmol), 3 (1 mmol), Cu-MOF (0.05 g), stirring at 60–70 °C.

b

Product yield.

c

Melting points of known cpds match with literature values.35,36