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Stereoselective Preparation of CF 3 -Containing Cyclopropanes.

Veronika MyronovaDominique CahardIlan Marek
Published in: Organic letters (2022)
A regio- and diastereoselective carbometalation of easily accessible CF 3 -substituted cyclopropenes is developed with a diastereoselectivity of the addition opposite to the CF 3 group. This simple strategy allows the preparation of polysubstituted (up to penta-) cyclopropyl rings possessing two adjacent quaternary carbon stereocenters with excellent diastereoselectivities.
Keyphrases
  • cystic fibrosis
  • molecularly imprinted
  • molecular docking
  • high resolution
  • mass spectrometry
  • molecular dynamics simulations