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- W4378781411 startingPage "4183" @default.
- W4378781411 abstract "An iminoiodane-enabled oxidative ring-opening of 2H-indazoles via C–N bond cleavage has been developed under metal-free reaction conditions. This methodology afforded a new array of unsymmetrical ortho-N-acylsulfonamidated azobenzenes with a wide functional group tolerance in good yields. The reaction potentially proceeds through the formation of a zwitterionic adduct, which is formed by the reaction between 2H-indazoles and iminoiodane." @default.
- W4378781411 created "2023-06-01" @default.
- W4378781411 creator A5027137508 @default.
- W4378781411 creator A5074084285 @default.
- W4378781411 date "2023-05-31" @default.
- W4378781411 modified "2023-10-01" @default.
- W4378781411 title "Imino-λ<sup>3</sup>-iodane-Triggered Oxidative Ring-Opening of 2<i>H</i>-Indazoles to <i>ortho</i>-<i>N</i>-Acylsulfonamidated Azobenzenes" @default.
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- W4378781411 doi "https://doi.org/10.1021/acs.orglett.3c01498" @default.
- W4378781411 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37255286" @default.
- W4378781411 hasPublicationYear "2023" @default.
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