4.2 Article

A new strategy for the one pot synthesis of (aryloxyimino)ethylcoumarins promoted by CuCl2

期刊

JOURNAL OF CHEMICAL RESEARCH
卷 -, 期 1, 页码 5-8

出版社

SCIENCE REVIEWS 2000 LTD
DOI: 10.3184/174751912X13247245983221

关键词

cross coupling; (aryloxyimino)ethylcoumarins; phenylboronic acid; cupric chloride

资金

  1. University of Calcutta
  2. CSIR, New Delhi, India [09/028(0792)/2010 EMR-I, 09/028(0768)/2010]
  3. DST-FIST, India

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Cupric chloride showed efficient catalytic activity for the cross coupling reaction of arylboronic acids and (hydroxyimino)ethylcoumarins at room temperature in the presence of NEt3 as base. A simple and convenient protocol for the synthesis of O-aryloxime ethers having the highly base sensitive coumarin nucleus is reported. O-Aryloxime ethers are important as they provide access to scaffolds for the generation of various biologically active compounds. They are potential precursors to benzofurans and benzisoxazoles.

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