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Cu-Catalyzed Enantioselective Protoboration of 2,3-Disubstituted 1,3-Dienes.

Sensheng LiuYangbin LiuArthur FlagetCheng ZhangClément Mazet
Published in: Organic letters (2023)
A Cu-catalyzed regio- and enantioselective protoboration of 2,3-disubstituted 1,3-dienes is described. The protocol operates under mild conditions and is applicable to symmetrically and unsymmetrically substituted dienes, providing access to homoallylic boronates in consistently high yield, regioselectivity, and enantiomeric ratio. Preliminary investigations point to a complex mechanism.
Keyphrases
  • room temperature
  • aqueous solution
  • randomized controlled trial
  • molecular docking
  • metal organic framework
  • ionic liquid