Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 6, Issue 6, Pages 1034-1039Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b717843c
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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.
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