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http://hdl.handle.net/10397/113282
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. |
Appears in Collections: | Journal/Magazine Article |
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