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Three-Component Borylallenylation of Alkynes: Access to Densely Boryl-Substituted Ene-allenes.

Shang-Hai YuTian-Jun GongYao Fu
Published in: Organic letters (2020)
Ene-allenes serve as versatile building blocks in organic synthesis, and the development of their efficient preparation is valuable. Herein the synthesis of boryl-substituted ene-allenes utilizing a Cu/Pd-catalyzed borylallenylation of alkynes with propargylic carbonates and bis(pinacolato)diboron is reported. Densely (tetra-, penta-, and hexa-) substituted ene-allenes were synthesized in acceptable yield with high regio- and stereoselectivity. More important molecule structures can be obtained by subsequent modifications.
Keyphrases
  • molecular docking
  • high resolution
  • room temperature
  • ionic liquid
  • molecularly imprinted
  • solid phase extraction