Highly stereoselective synthesis of 2-methyl-1,3-dienes by palladium-catalyzed cross-coupling reaction with trimethylaluminum

Masahiro Miyazawa*, Risa Takehana, Takao Sanga, Aoi Hosomori, Hajime Yokoyama, Yoshiro Hirai

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Palladium-catalyzed cross-coupling reaction using tricyclohexylphosphine can be used to convert a range of 2-bromo-1,3-dienes efficiently and selectively to the corresponding methyl-branched conjugated dienes.

Original languageEnglish
Article numberST-2013-U0962-L
Pages (from-to)531-534
Number of pages4
JournalSynlett
Volume25
Issue number4
DOIs
StatePublished - 2014/03

Keywords

  • alkylation
  • conjugated diene
  • cross-coupling
  • isomerization
  • palladium catalyst

ASJC Scopus subject areas

  • Organic Chemistry
  • Drug Discovery

Fingerprint

Dive into the research topics of 'Highly stereoselective synthesis of 2-methyl-1,3-dienes by palladium-catalyzed cross-coupling reaction with trimethylaluminum'. Together they form a unique fingerprint.

Cite this