• Media type: E-Article
  • Title: Palladium-catalyzed Sonogashira coupling reactions in γ-valerolactone-based ionic liquids
  • Contributor: Orha, László; Tukacs, József M; Kollár, László; Mika, László T
  • imprint: Beilstein Institut, 2019
  • Published in: Beilstein Journal of Organic Chemistry
  • Language: English
  • DOI: 10.3762/bjoc.15.284
  • ISSN: 1860-5397
  • Keywords: Organic Chemistry
  • Origination:
  • Footnote:
  • Description: <jats:p>It was demonstrated that the γ-valerolactone-based ionic liquid, tetrabutylphosphonium 4-ethoxyvalerate as a partially bio-based solvent can be utilized as alternative reaction medium for copper- and auxiliary base-free Pd-catalyzed Sonogashira coupling reactions of aryl iodides and functionalized acetylenes under mild conditions. Twenty-two cross-coupling products were isolated with good to excellent yields (72–99%) and purity (&gt;98%). These results represent an example which proves that biomass-derived safer solvents can be utilized efficiently in common, industrially important transformations exhibiting higher chemical and environmental efficiency.</jats:p>
  • Access State: Open Access