Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/113282
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Title: Transition-metal free photocatalytic synthesis of acylsulfonamides
Authors: Lam, LY 
Ma, C 
Issue Date: 9-May-2025
Source: Organic letters, 9 May 2025, v. 27, no. 18, p. 4732-4736
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.
Publisher: American Chemical Society
Journal: Organic letters 
ISSN: 1523-7060
EISSN: 1523-7052
DOI: 10.1021/acs.orglett.5c01129
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/).
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.
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