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- W2121782904 endingPage "6219" @default.
- W2121782904 startingPage "6216" @default.
- W2121782904 abstract "Hypervalent-iodine-mediated oxidative coupling of the two aryl groups in either 2-acylamino-N-phenyl-benzamides or 2-hydroxy-N-phenylbenzamides, with concomitant insertion of the ortho-substituted N or O atom into the tether, has been described for the first time. This unusual metal-free rearrangement reaction involves an oxidative C(sp2)C(sp2) aryl–aryl bond formation, cleavage of a C(sp2)C(O) bond, and a lactamization/lactonization. Furthermore, unsymmetrical diaryl compounds can be easily obtained by removing the tether within the cyclized product." @default.
- W2121782904 created "2016-06-24" @default.
- W2121782904 creator A5044143169 @default.
- W2121782904 creator A5064663421 @default.
- W2121782904 creator A5068638985 @default.
- W2121782904 creator A5070040024 @default.
- W2121782904 date "2014-04-24" @default.
- W2121782904 modified "2023-10-07" @default.
- W2121782904 title "Intramolecular Metal-Free Oxidative Aryl-Aryl Coupling: An Unusual Hypervalent-Iodine-Mediated Rearrangement of 2-Substituted<i>N</i>-Phenylbenzamides" @default.
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- W2121782904 doi "https://doi.org/10.1002/anie.201402925" @default.
- W2121782904 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24764255" @default.
- W2121782904 hasPublicationYear "2014" @default.