Palladium(II)-Catalyzed meta-C-H Olefination: Constructing Multisubstituted Arenes through Homo-Diolefination and Sequential Hetero-Diolefination

Milan Bera, Arun Maji, Santosh K. Sahoo, Debabrata Maiti

Research output: Contribution to journalArticlepeer-review

214 Scopus citations

Abstract

Divinylbenzene derivatives represent an important class of molecular building blocks in organic chemistry and materials science. Reported herein is the palladium-catalyzed synthesis of divinylbenzenes by meta-C-H olefination of sulfone-based arenes. Successful sequential olefinations in a position-selective manner provided a novel route for the synthesis of hetero-dialkenylated products, which are difficult to access using conventional methods. Additionally, 1,3,5-trialkenylated compounds can be generated upon successful removal of the directing group. Jockeying for position: Reported herein is the palladium-catalyzed synthesis of mono- and divinylbenzenes by meta-C-H olefination of benzyl sulfones. Successful sequential olefinations in a position-selective manner provided a novel route for the synthesis of hetero-dialkenylated products, which are difficult to access using conventional methods. DG=directing group.

Original languageEnglish
Pages (from-to)8515-8519
Number of pages5
JournalAngewandte Chemie - International Edition
Volume54
Issue number29
DOIs
StatePublished - Jul 13 2015

Bibliographical note

Publisher Copyright:
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Keywords

  • C-H activation
  • olefination
  • palladium
  • sulfur
  • synthetic methods

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry

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