Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/113282
DC Field | Value | Language |
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dc.contributor | Department of Applied Biology and Chemical Technology | en_US |
dc.creator | Lam, LY | en_US |
dc.creator | Ma, C | en_US |
dc.date.accessioned | 2025-06-02T06:57:20Z | - |
dc.date.available | 2025-06-02T06:57:20Z | - |
dc.identifier.issn | 1523-7060 | en_US |
dc.identifier.uri | http://hdl.handle.net/10397/113282 | - |
dc.language.iso | en | en_US |
dc.publisher | American Chemical Society | en_US |
dc.rights | Copyright © 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.rights | The 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.title | Transition-metal free photocatalytic synthesis of acylsulfonamides | en_US |
dc.type | Journal/Magazine Article | en_US |
dc.identifier.spage | 4732 | en_US |
dc.identifier.epage | 4736 | en_US |
dc.identifier.volume | 27 | en_US |
dc.identifier.issue | 18 | en_US |
dc.identifier.doi | 10.1021/acs.orglett.5c01129 | en_US |
dcterms.abstract | We 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.accessRights | open access | en_US |
dcterms.bibliographicCitation | Organic letters, 9 May 2025, v. 27, no. 18, p. 4732-4736 | en_US |
dcterms.isPartOf | Organic letters | en_US |
dcterms.issued | 2025-05-09 | - |
dc.identifier.scopus | 2-s2.0-105004061907 | - |
dc.identifier.pmid | 40306757 | - |
dc.identifier.eissn | 1523-7052 | en_US |
dc.description.validate | 202505 bchy | en_US |
dc.description.oa | Version of Record | en_US |
dc.identifier.FolderNumber | OA_TA | - |
dc.description.fundingSource | RGC | en_US |
dc.description.fundingSource | Others | en_US |
dc.description.fundingText | Hong 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.pubStatus | Published | en_US |
dc.description.TA | ACS (2025) | en_US |
dc.description.oaCategory | TA | en_US |
Appears in Collections: | Journal/Magazine Article |
Files in This Item:
File | Description | Size | Format | |
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Lam_Transition_Metal_Free.pdf | 2.03 MB | Adobe PDF | View/Open |
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