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Chemoselective Reduction of Azlactones Using Schwartz's Reagent.

Danielle L J PinheiroEloah P ÁvilaGabriel M F BatistaGiovanni Wilson Amarante
Published in: The Journal of organic chemistry (2017)
Highly chemoselective addition of Schwartz's reagent to widely available azlactones is described. This method allows the preparation of challenged functionalized α-amino aldehydes, in good to high isolated yields at room temperature, after only 2 min reaction. The presence of sensitive functionalities or electronic factors does not compromise the potential of the method. The use of an excess of the reducing reagent gave a very functionalized allylic alcohol derivative in 86% yield.
Keyphrases
  • room temperature
  • molecularly imprinted
  • quantum dots
  • ionic liquid
  • high resolution
  • climate change
  • tandem mass spectrometry