Synthesis of ortho-Phenolic Sulfilimines via an Intermolecular Sulfur Atom Transfer Cascade Reaction

To expand the toolbox for the synthesis of ortho-phenolic sulfilimines, sigmatropic rearrangements were introduced to the field of sulfilimine chemistry. Herein we report a N–H sulfenylation/[2,3]-sigmatropic rearrangement cascade reaction. This mild reaction enables commercially available thiols to...

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Veröffentlicht in:Organic letters 2020-05, Vol.22 (10), p.3799-3803
Hauptverfasser: Xiong, Feng, Zuo, Yingying, Song, Yinan, Zhang, Linxing, Zhang, Xinhao, Xu, Shaojian, Ren, Yan
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Sprache:eng
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Zusammenfassung:To expand the toolbox for the synthesis of ortho-phenolic sulfilimines, sigmatropic rearrangements were introduced to the field of sulfilimine chemistry. Herein we report a N–H sulfenylation/[2,3]-sigmatropic rearrangement cascade reaction. This mild reaction enables commercially available thiols to serve as the sulfenylation reagent and generates water as the sole byproduct. Moreover, the reaction has a wide substrate scope and can be conducted on a gram scale with excellent reaction efficiency.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.0c01032