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March 31, 2026Bioconjugate Chemistry2 citations

Ugi-Type Reaction Enables Access to Fused Imidazole Derivatives for DNA-Encoded Library Technology

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HGHao GuoZLZitao LiGWGaonan Wang

Key Points

  • The research aims to develop a DNA-compatible method for synthesizing diverse N-fused imidazopyridines using a Ugi-type reaction.
  • Catalyst-free Ugi-type multicomponent reaction
  • Use of TMSCN as a functional isonitrile equivalent
  • Desilylation activation in water
  • Broad substrate scope for aldehydes and heterocyclic amidines
  • Achieved diverse synthesis of N-fused imidazopyridines
  • Exhibited excellent chemoselectivity
  • Demonstrated efficient reaction without additional catalysts

Abstract

This study presents a DNA-compatible synthesis of diverse N-fused imidazopyridines via a catalyst-free Ugi-type multicomponent reaction using TMSCN as a functional isonitrile equivalent. The desilylation activation occurs efficiently in water without additional catalysts. The method exhibits a broad substrate scope for aldehydes and heterocyclic amidines and excellent chemoselectivity, underscoring its utility for constructing privileged heteroaromatic scaffolds in DNA-encoded library technology.

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Cite This Study

Guo et al. (2026) studied this question.

synapsesocial.com/papers/69cb645fe6a8c024954b8aa7https://doi.org/10.1021/acs.bioconjchem.5c00655
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