4.8 Article

Rh(III)-Catalyzed Synthesis of Multisubstituted Isoquinoline and Pyridine N-Oxides from Oximes and Diazo Compounds

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 33, 页码 12204-12207

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AMER CHEMICAL SOC
DOI: 10.1021/ja406338r

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资金

  1. Alexander von Humboldt Foundation
  2. European Research Council under the European Community/ERC [25936]
  3. DFG

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Multisubstituted isoquinoline and pyridine N-oxides have been prepared by Rh(III)-catalyzed cyclization of oximes and diazo compounds via aryl and vinylic C-H activation. This intermolecular annulation involving tandem C-H activation, cyclization, and condensation steps proceeds under mild conditions, obviates the need for oxidants, releases N-2 and H2O as the byproducts, and displays a broad substituent scope.

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