Anti-Markovnikov Addition of Anilines to Aliphatic Terminal Alkynes Catalyzed by an 8-Quinolinolato Rhodium Complex

Yoshihiko Morimoto, Takuya Kochi, Fumitoshi Kakiuchi

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Anti-Markovnikov addition of anilines to aliphatic terminal alkynes proceeded using an 8-quinolinolato rhodium/phosphine catalyst system. The use of a strong organic base, 1,1,3,3,–tetramethylguanidine, in the catalyst system enabled the formation of the aldimine products. Substrates with various functional groups including polar groups such as a phenolic hydroxy group are applicable to the hydroamination.

Original languageEnglish
Article numbere2100125
JournalHelvetica Chimica Acta
Volume104
Issue number10
DOIs
Publication statusPublished - 2021 Oct

Keywords

  • 8-quinolinolate ligand
  • aldimines
  • aliphatic terminal alkynes
  • alkynes
  • anilines
  • anti-Markovnikov addition
  • rhodium

ASJC Scopus subject areas

  • Catalysis
  • Biochemistry
  • Drug Discovery
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

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