2-(2-Bromoaryl)imidazoles
react with cyclohexane-1,3-diones in
the presence of a catalytic amount of recyclable Fe
3
O
4
@SiO
2
@MOF-199 and a base to give the corresponding
C–C coupled and cyclized products 6,7-dihydroimidazo[1,2-
f
]phenanthridin-8(5
H
)-ones in high yields.
The magnetic MOF catalyst could be easily recovered and reused four
times without any significant loss of catalytic activity. The coupled
and cyclized scaffolds were aromatized to imidazo[1,2-
f
]phenanthridines in high yields by a one-pot sequential procedure
including reduction, dehydration, and oxidation. The present protocol
could be applied to the synthesis of Zephycandidine A, which is known
to exhibit anti-tumor activity.