4.7 Article

Cu(II)-Catalyzed 6π-Photocyclization of Dienynes

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 81, 期 24, 页码 12553-12558

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AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.6b02537

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资金

  1. International Science AMP
  2. Technology Cooperation Program of China [2014DFE40130]
  3. National Nature Science Foundation of China [21274023]

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The first 6 pi-photocyclization of dienynes was developed, which provides a new and effective protocol for the synthesis of the phenyl ring in excellent yields with nice functional group tolerance. In this transformation, the Cu(OTf)(2) catalyst plays a key role in the conversion of alkyne moiety into an alkene-type moiety, which means that the dienyne reactant is converted into a triene-type substrate. Thus, this reaction proceeds via a Cu(II)-catalyzed 6 pi-photocyclization of triene-type derivatives.

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