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Divergent synthesis of N-heterocyclic 1,6-enynes through a zinc-catalyzed decarboxylative A3 reaction.

Zhuo-Ya MaoYi-Wen LiuRui-Jun MaJian-Liang YeChang-Mei SiChang-Mei SiGuo-Qiang Lin
Published in: Chemical communications (Cambridge, England) (2019)
A zinc-catalyzed decarboxylative A3 reaction of cyclic amino acids, α,β-unsaturated aldehydes and terminal alkynes has been developed. A series of functionalized N-heterocyclic 1,6-enynes have been successfully obtained with excellent regioselectivities through this novel approach. In addition, the utility of this straightforward process is demonstrated by the preparation of a polycyclic nitrogen-containing heterocyclic compound.
Keyphrases
  • room temperature
  • amino acid
  • oxide nanoparticles
  • molecularly imprinted
  • visible light
  • high resolution
  • mass spectrometry
  • ionic liquid
  • simultaneous determination