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Heteroannulation of 3-Nitroindoles and 3-Nitrobenzo[b]thiophenes: A Multicomponent Approach toward Pyrrole-Fused Heterocycles.

P V SanthiniSheba Ann BabuAkhil Krishnan RE SureshJubi John
Published in: Organic letters (2017)
A simple, efficient, and general multicomponent reaction involving an enolizable ketone, a primary amine, and an N-protected 3-nitroindole was developed for the synthesis of a range of functionalized pyrrolo[3,2-b]indoles. The methodology was efficaciously utilized for the "pyrroloindoliztion" of natural products, the pyrrolization of 3-nitrobenzo[b]thiophene, and the gram-scale synthesis of pyrroloindole. Furthermore, a "one-pot" approach for accessing indolo[3,2-b]indoles was realized.
Keyphrases
  • quantum dots
  • molecularly imprinted
  • mass spectrometry
  • tandem mass spectrometry