Arylation of chloroanthraquinones by surprisingly facile Suzuki-Miyaura cross-coupling reactions

Thies Thiemann, Yasuko Tanaka, Jesus Iniesta, H. Tresa Varghese, C. Yohannan Pannicker

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)

Abstract

Chloroanthraquinones were found to undergo facile Suzuki-cross coupling with substituted phenyl boronic acids using a commercial catalyst Pd(PPh 3)4 and with Pd(PPh3)4 prepared in situ from Pd(PPh3)2Cl2 and PPh3.

Original languageEnglish
Pages (from-to)732-736
Number of pages5
JournalJournal of Chemical Research
Issue number12
DOIs
Publication statusPublished - 2009

Keywords

  • Anthraquinones
  • Chloroarenes
  • Suzuki-Miyaura cross-coupling
  • Tetrakis(triphenylphosphino)palladium

ASJC Scopus subject areas

  • General Chemistry

Fingerprint

Dive into the research topics of 'Arylation of chloroanthraquinones by surprisingly facile Suzuki-Miyaura cross-coupling reactions'. Together they form a unique fingerprint.

Cite this