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A Brønsted acid catalyzed tandem reaction for the diastereoselective synthesis of cyclobuta-fused tetrahydroquinoline carboxylic esters.

Valentina MarrasPierluigi CaboniFrancesco SecciRegis GuillotDavid J AitkenAngelo Frongia
Published in: Organic & biomolecular chemistry (2021)
A novel Brønsted acid catalyzed tandem reaction provides highly functionalized cyclobuta-fused tetrahydroquinoline carboxylic esters from anilines and 2-alkylenecyclobutanones in good to high yield. During the reaction a dynamic diastereoselective cyclization is achieved, resulting in the formation of three contiguous stereocenters with high stereoselectivity.
Keyphrases
  • room temperature
  • quantum dots
  • high resolution
  • molecularly imprinted
  • simultaneous determination