Simple two-step synthesis of 2,4-disubstituted pyrroles and 3,5-disubstituted pyrrole-2-carbonitriles from enones

@article{Kucukdisli2014SimpleTS,
  title={Simple two-step synthesis of 2,4-disubstituted pyrroles and 3,5-disubstituted pyrrole-2-carbonitriles from enones},
  author={Murat Kucukdisli and Dorota Ferenc and Marcel Heinz and Christine A. Wiebe and Till Opatz},
  journal={Beilstein Journal of Organic Chemistry},
  year={2014},
  volume={10},
  pages={466 - 470}
}
Summary The cyclocondensation of enones with aminoacetonitrile furnishes 3,4-dihydro-2H-pyrrole-2-carbonitriles which can be readily converted to 2,4-disubstituted pyrroles by microwave-induced dehydrocyanation. Alternatively, oxidation of the intermediates produces 3,5-disubstituted pyrrole-2-carbonitriles. 
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