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Catalytic Asymmetric [4+2]-Cycloadditions Using Tropolones: Developments, Scope, Transformations, and Bioactivity.

Niels HammerJeremy D EricksonVibeke H LauridsenJoakim B JakobsenBente K HansenKristian M JacobsenThomas B PoulsenKarl Anker Jørgensen
Published in: Angewandte Chemie (International ed. in English) (2018)
An organocatalyzed asymmetric [4+2]-cycloaddition between tropolones and electron-deficient dienophiles is presented. Complex and biologically interesting dihydrohomobarrelenone scaffolds are formed through a Diels-Alder reaction utilizing bifunctional Brønsted-base catalysis, affording the corresponding bridged bicyclic cycloadducts in up to quantitative yields with good enantio- (up to 92 % ee) and diastereoselectivity (up to >20:1 d.r.). The synthetic value of the obtained products is explored by downstream transformations, including photoisomerizations, and their biological relevancy by in vivo testing in MCF-7 cancer cells.
Keyphrases
  • solid state
  • breast cancer cells
  • high resolution
  • electron transfer
  • tissue engineering
  • highly efficient
  • mass spectrometry
  • crystal structure
  • metal organic framework