4.7 Article

C-H nitrogenation and oxygenation by ruthenium catalysis

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CHEMICAL COMMUNICATIONS
卷 50, 期 1, 页码 29-39

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc47028h

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  1. Humboldt Foundation
  2. European Research Council
  3. Fonds der Chemischen Industrie

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Remarkable recent progress has been accomplished in direct C-H functionalizations for the formation of C-N and C-O bonds through the use of readily accessible ruthenium catalysts. Particularly, ruthenium(II) complexes allowed for challenging direct C(sp(2))-H hydroxylation of arenes. These catalysts set the stage for step-economical C-H functionalization with electron-rich as well as electron-deficient (hetero) arenes and, therefore, provided versatile access to diversely decorated phenols. While a number of synthetically useful protocols for ruthenium-catalyzed C(sp(3))-H bond nitrogenation have been elaborated, the analogous transformations of more stable C(sp(2))-H bonds were very recently achieved.

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