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[3 + 2] cycloaddition of nonstabilized azomethine ylides and 2-benzothiazolamines to access imidazolidine derivatives.

Kai-Kai WangYan-Li LiMing-Yue WangJun JingZhan-Yong WangRongxiang Chen
Published in: RSC advances (2022)
A simple and practical method for the construction of 1,3,5-trisubstituted imidazolidine derivatives via [3 + 2] cycloaddition reaction has been developed. This reaction could smoothly proceed between nonstabilized azomethine ylides generated in situ and 2-benzothiazolamines to deliver a wide scope of differently substituted imidazolidines in high yields (up to 98%). The structure of one example was confirmed by X-ray single-crystal structure analysis.
Keyphrases
  • crystal structure
  • high resolution
  • molecular docking
  • structure activity relationship
  • magnetic resonance imaging
  • magnetic resonance
  • computed tomography
  • mass spectrometry
  • electron transfer