Efficient synthesis of diverse hetero-bis-metallated alkenes as modular reagents towards highly conjugated and isolated olefinic systems

Chem Commun (Camb). 2012 Aug 25;48(66):8267-9. doi: 10.1039/c2cc34052f. Epub 2012 Jul 13.

Abstract

An efficient synthesis of diverse hetero-bis-metallated alkenes with conjugated and isolated olefin subunits is reported. Relying on those useful tin/boron reagents a convergent, palladium-catalyzed fragment coupling strategy has been developed as an elegant methodology to construct highly conjugated polyenes and stabilized olefinic analogues thereof. The utility of these reagents was further demonstrated in a concise and modular construction of extended polyene side chains of the potent polyketide antibiotic etnangien.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemical synthesis*
  • Alkenes / chemistry
  • Anti-Bacterial Agents / chemical synthesis
  • Macrolides / chemical synthesis
  • Macrolides / chemistry
  • Molecular Structure
  • Palladium / chemistry*
  • Polyenes / chemical synthesis
  • Polyenes / chemistry

Substances

  • Alkenes
  • Anti-Bacterial Agents
  • Macrolides
  • Polyenes
  • etnangien
  • Palladium