Rh-catalyzed transannulation of pyridotriazoles with alkynes and nitriles

Stepan Chuprakov, Frank W. Hwang, Vladimir Gevorgyan

Research output: Contribution to journalArticle

197 Citations (Scopus)

Abstract

(Chemical Equation Presented) Changing the rings: A variety of N-fused pyrrolo- and imidazopyridines can be readily formed by a direct Rh-catalyzed transannulation of pyridotriazoles with alkynes and nitriles, respectively (see scheme). Substituted pyridotriazoles can also serve as stable precursors for Rh carbenoids, the preparation of which does not require special precautions or slow-addition techniques.

Original languageEnglish (US)
Pages (from-to)4757-4759
Number of pages3
JournalAngewandte Chemie - International Edition
Volume46
Issue number25
DOIs
StatePublished - Jul 4 2007
Externally publishedYes

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Nitriles
Alkynes

Keywords

  • Annulation
  • Nitrogen heterocycles
  • Rhodium
  • Synthetic methods
  • Triazoles

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)

Cite this

Rh-catalyzed transannulation of pyridotriazoles with alkynes and nitriles. / Chuprakov, Stepan; Hwang, Frank W.; Gevorgyan, Vladimir.

In: Angewandte Chemie - International Edition, Vol. 46, No. 25, 04.07.2007, p. 4757-4759.

Research output: Contribution to journalArticle

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