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Organocatalytic Asymmetric Tamura Cycloaddition with α- Branched Nitroolefins: Synthesis of Functionalized 1-Tetralones.

Utpal NathSubhas Chandra Pan
Published in: The Journal of organic chemistry (2017)
A new catalytic asymmetric Tamura cycloaddition with nitroolefins was developed. This demonstration of the reaction of α-branched nitroolefins with homophthalic anhydrides delivers highly functionalized 1-tetralone compounds. With bifunctional squaramide catalyst, the desired tetralone products are obtained with high enantioselectivity and good diastereoselectivity.
Keyphrases
  • quantum dots
  • highly efficient
  • molecularly imprinted
  • metal organic framework
  • solid state
  • ionic liquid
  • room temperature
  • reduced graphene oxide
  • simultaneous determination