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Electrochemical Radical-Radical Cross-Coupling Approach between Sodium Sulfinates and 2 H-Indazoles to 3-Sulfonylated 2 H-Indazoles

Authors
Kim, W.Kim, H.Y.Oh, K.
Issue Date
Aug-2020
Publisher
American Chemical Society
Citation
Organic Letters, v.22, no.16, pp 6319 - 6323
Pages
5
Journal Title
Organic Letters
Volume
22
Number
16
Start Page
6319
End Page
6323
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/53626
DOI
10.1021/acs.orglett.0c02144
ISSN
1523-7060
1523-7052
Abstract
A direct cross-coupling between sodium sulfinates and 2H-indazoles has been developed under electrochemical conditions. The utilization of a graphite anode and platinum cathode in an undivided cell with a constant current of 7 mA allowed the concurrent oxidations of sulfinates and 2H-indazoles to sulfonyl radical and radical cationic 2H-indazoles, facilitating the direct radical-radical coupling strategy to 3-sulfonylated 2H-indazole derivatives. The transition-metal- A nd redox-reagent-free synthetic approach should serve as a valuable synthetic tool to achieve heteroaromatic compounds. Copyright © 2020 American Chemical Society.
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