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Synthesis of Polysubstituted Pyrroles through a Formal [4 + 1] Cycloaddition/E1cb Elimination/Aromatization Sequence of Sulfur Ylides and α,β-Unsaturated Imines.

Bei-Yi ChengYa-Ni WangTian-Ren LiLiang-Qiu LuWen-Jing Xiao
Published in: The Journal of organic chemistry (2017)
A reaction sequence comprising a formal [4 + 1] cycloaddition, an E1cb elimination, and an aromatization process is described in this work. By doing so, polysubstituted pyrroles were achieved from easily available chemicals, sulfur ylides, and α,β-unsaturated imines. This protocol features mild conditions, high efficiency, and wide substrate scopes.
Keyphrases
  • high efficiency
  • amino acid
  • randomized controlled trial
  • structural basis