Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/113282
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorLam, LYen_US
dc.creatorMa, Cen_US
dc.date.accessioned2025-06-02T06:57:20Z-
dc.date.available2025-06-02T06:57:20Z-
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://hdl.handle.net/10397/113282-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsCopyright © 2025 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0 (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Lam, L. Y., & Ma, C. (2025). Transition-Metal Free Photocatalytic Synthesis of Acylsulfonamides. Organic Letters, 27(18), 4732-4736 is available at https://doi.org/10.1021/acs.orglett.5c01129.en_US
dc.titleTransition-metal free photocatalytic synthesis of acylsulfonamidesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage4732en_US
dc.identifier.epage4736en_US
dc.identifier.volume27en_US
dc.identifier.issue18en_US
dc.identifier.doi10.1021/acs.orglett.5c01129en_US
dcterms.abstractWe have developed a transition-metal-free photocatalytic S-N coupling reaction utilizing sodium organosulfinate and hydroxamic acid to synthesize acylsulfonamides. Employing 2,3,5,6-tetra(9H-carbazol-9-yl)benzonitrile (4CzBN) as a photocatalyst, this method enables the preparation of a wide range of acylsulfonamides from arylhydroxamic acids or N-hydroxycarbamates. Mechanistic studies indicate that the generation of singlet oxygen (1O2) via the Energy Transfer Process (EnT) is crucial for facilitating the reaction. This approach offers a sustainable and efficient pathway for acylsulfonamide synthesis under mild conditions.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOrganic letters, 9 May 2025, v. 27, no. 18, p. 4732-4736en_US
dcterms.isPartOfOrganic lettersen_US
dcterms.issued2025-05-09-
dc.identifier.scopus2-s2.0-105004061907-
dc.identifier.pmid40306757-
dc.identifier.eissn1523-7052en_US
dc.description.validate202505 bchyen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_TA-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextHong Kong Polytechnic University (State Key Laboratory of Chemical Biology and Drug Discovery and PolyU Marshall Research Centre for Medical Microbial Biotechnology).en_US
dc.description.pubStatusPublisheden_US
dc.description.TAACS (2025)en_US
dc.description.oaCategoryTAen_US
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