A simple and convenient synthesis of di(E)-arylidene-tetralone-spiro-glutarimides from Baylis–Hillman acetates via an interesting biscyclization strategy involving facile C–C and C–N bond formation is described. Also, one-pot multistep transformation of the Baylis–Hillman acetates into di(E)-arylidene-spiro-bisglutarimides is presented.
D. Basavaiah and R. J. Reddy, Org. Biomol. Chem., 2008, 6, 1034 DOI: 10.1039/B717843C
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