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. 2021 Jan 21;11(8):4339–4355. doi: 10.1039/d0ra09420j

One-pot three-component synthesis of various xanthene derivatives catalysed by Fe3O4@NFC@NNSM-Mn(iii)a.

graphic file with name d0ra09420j-u2.jpg
Entry Aldehyde R 1 Product Time (min) Yieldb (%) MP (°C)
Found Reported
1 (ref. 53) graphic file with name d0ra09420j-u3.jpg H graphic file with name d0ra09420j-u4.jpg 10 98 203–204 203–205
2 (ref. 53) graphic file with name d0ra09420j-u5.jpg H graphic file with name d0ra09420j-u6.jpg 15 95 229–230 228–230
3 (ref. 54) graphic file with name d0ra09420j-u7.jpg H graphic file with name d0ra09420j-u8.jpg 15 92 205–206 206–207
4 (ref. 53) graphic file with name d0ra09420j-u9.jpg H graphic file with name d0ra09420j-u10.jpg 10 95 259–261 260–261
5 (ref. 55) graphic file with name d0ra09420j-u11.jpg H graphic file with name d0ra09420j-u12.jpg 10 97 205–206 205–206
6 (ref. 56) graphic file with name d0ra09420j-u13.jpg Me graphic file with name d0ra09420j-u14.jpg 10 96 203–204 202–204
7 (ref. 57) graphic file with name d0ra09420j-u15.jpg Me graphic file with name d0ra09420j-u16.jpg 10 95 169–170 168–170
8 (ref. 58) graphic file with name d0ra09420j-u17.jpg Me graphic file with name d0ra09420j-u18.jpg 10 96 200–201 201–202
9 (ref. 59) graphic file with name d0ra09420j-u19.jpg Me graphic file with name d0ra09420j-u20.jpg 20 93 295–297 >300
10 (ref. 60) graphic file with name d0ra09420j-u21.jpg H graphic file with name d0ra09420j-u22.jpg 30 80 267–269 268–269
11 (ref. 61) graphic file with name d0ra09420j-u23.jpg Me graphic file with name d0ra09420j-u24.jpg 25 85 155–157
12 graphic file with name d0ra09420j-u25.jpg H graphic file with name d0ra09420j-u26.jpg 15 90 168–170 New
13 graphic file with name d0ra09420j-u27.jpg Me graphic file with name d0ra09420j-u28.jpg 15 92 200–202 New
14 graphic file with name d0ra09420j-u29.jpg H graphic file with name d0ra09420j-u30.jpg 15 92 220–222 New
15 graphic file with name d0ra09420j-u31.jpg Me graphic file with name d0ra09420j-u32.jpg 20 95 250–252 New
a

Reaction conditions: benzaldehyde (1.0 mmol), dimedone (2.0 mmol) and catalyst (0.5 mol%) and EtOH (3 ml), 45 °C.

b

Isolated yield.