Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 88, Issue 4, Pages 2666-2669Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.3c00012
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N-Alkyl sulfoximines react with in situ generated arynes under mild conditions to afford o-sulfinylanilines in good yields. The transformation exhibits a wide substrate scope and excellent functional group tolerance. The structure of a reaction product was confirmed by single-crystal X-ray diffraction.
N-Alkyl sulfoximines react with arynes generated in situ under mild conditions providing o-sulfinylanilines in good yields. The transformation is characterized by a broad substrate scope and a good functional group tolerance. The structure of a reaction product was confirmed by single-crystal X-ray diffraction.
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