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Mild and phosphine-free iron-catalyzed cross-coupling of nonactivated secondary alkyl halides with alkynyl grignard reagents

  • Chi Wai Cheung
  • , Peng Ren
  • , Xile Hu*
  • *Corresponding author for this work
  • Swiss Federal Institute of Technology Lausanne

Research output: Contribution to journalArticlepeer-review

Abstract

A simple protocol for iron-catalyzed cross-coupling of nonactivated secondary alkyl bromides and iodides with alkynyl Grignard reagents at room temperature has been developed. A wide range of secondary alkyl halides and terminal alkynes are tolerated to afford the substituted alkynes in good yields. A slight modification of the reaction protocol also allows for cross-coupling with a variety of primary alkyl halides.

Original languageEnglish
Pages (from-to)2566-2569
Number of pages4
JournalOrganic Letters
Volume16
Issue number9
DOIs
StatePublished - 2 May 2014
Externally publishedYes

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