4.2 Article

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

期刊

JOURNAL OF CHEMICAL RESEARCH
卷 -, 期 12, 页码 732-736

出版社

SAGE PUBLICATIONS LTD
DOI: 10.3184/030823409X12586584303880

关键词

chloroarenes; anthraquinones; Suzuki-Miyaura cross-coupling; tetrakis(triphenylphosphino)palladium

资金

  1. Global Centre of Excellence on New Carbon Resources, Kyushu University, Japan

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

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