Benzisothiazol‐3‐ones through a Metal‐Free Intramolecular N–S Bond Formation

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dc.contributor.authorYang, Ke
dc.contributor.authorZhang, Hao
dc.contributor.authorNiu, Ben
dc.contributor.authorTang, Tiandi
dc.contributor.authorGe, Haibo
dc.contributor.departmentChemistry and Chemical Biology, School of Scienceen_US
dc.date.accessioned2019-06-13T19:36:49Z
dc.date.available2019-06-13T19:36:49Z
dc.date.issued2018-11
dc.description.abstractThe highly efficient synthesis of benzoisothiazol‐3‐ones from thiobenzamides has been described with good functional group compatibility and excellent yields. This work represents the first example of selectfluor‐promoted N–S bond formation processes. This method provides a facile approach to access various important bioactive benzoisothiazol‐3‐ones.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationYang, K., Zhang, H., Niu, B., Tang, T., & Ge, H. (2018). Benzisothiazol-3-ones through a Metal-Free Intramolecular N–S Bond Formation. European Journal of Organic Chemistry, 2018(40), 5520–5523. https://doi.org/10.1002/ejoc.201801090en_US
dc.identifier.urihttps://hdl.handle.net/1805/19609
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1002/ejoc.201801090en_US
dc.relation.journalEuropean Journal of Organic Chemistryen_US
dc.rightsPublisher Policyen_US
dc.sourceAuthoren_US
dc.subjectcleavage reactionsen_US
dc.subjectcyclizationen_US
dc.subjectsynthetic methodsen_US
dc.titleBenzisothiazol‐3‐ones through a Metal‐Free Intramolecular N–S Bond Formationen_US
dc.typeArticleen_US
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