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Total synthesis of applanatumol A.

Kyohei UchidaYuichiro KawamotoToyoharu KobayashiHisanaka Ito
Published in: Chemical communications (Cambridge, England) (2023)
The first total synthesis of applanatumol A has been achieved in a highly stereocontrolled manner. The synthetic method includes assembly of the contiguous chiral centers by convergent Fráter-Seebach alkylation, construction of the seven-membered ring by intramolecular aldol reaction, and stereoselective tandem cyclization to form the tetracyclic skeleton.
Keyphrases
  • capillary electrophoresis
  • ionic liquid
  • energy transfer
  • mass spectrometry