The Michael reaction of acetophenones with trans-dibenzoylethylene

Starting from 2,5‐bisarylidenecyclopentanone and malononitrile (1:1) several novel pyrindine derivatives were synthesized by a facile and convenient one‐pot reaction using sodium ethoxide in absolute ethanol at room temperature. The structure of the reaction products was unambiguously deduced ftom their infrared, 1H‐nuclear magnetic resonance spectroscopy, elemental analysis and single crystal X‐ray crystallography.

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Saturated and partially unsaturated carbocycles

Booker‐Milburn¹,

Sharpe²

1998

J. Chem. Soc., Perkin Trans. 1

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The Michael reaction of acetophenones with trans-dibenzoylethylene

Cited by 6 publications

References 18 publications

ChemInform Abstract: The Michael Reaction of Acetophenones with trans‐Dibenzoylethylene.

ChemInform Abstract: The Michael Reaction of Acetophenones with trans‐Dibenzoylethylene.

Synthesis of novel pyrindine derivatives from a facile reaction of 2,5‐bisarylidenecyclopentanone and malononitrile

Saturated and partially unsaturated carbocycles

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