Electro-oxidation induced O-S cross-coupling of quinoxalinones with sodium sulfinates for synthesizing 2-sulfonyloxylated quinoxalines
The functionalization of quinoxalinones is synthetically and biologically appealing, however, C2 functionalized quinoxalinones is not reported via environmentally friendly approach. Herein, we disclosed C2-O sulfonylation of quinoxalinones via our developed electrochemical oxidative O-S coupling str...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2022-11, Vol.58 (88), p.12357-1236 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The functionalization of quinoxalinones is synthetically and biologically appealing, however, C2 functionalized quinoxalinones is not reported
via
environmentally friendly approach. Herein, we disclosed C2-O sulfonylation of quinoxalinones
via
our developed electrochemical oxidative O-S coupling strategy for synthesizing 2-sulfonyloxylated quinoxalines. Applying this protocol, quinoxalin-ones and sodium sulfinates as the starting materials, a wide range of 2-sulfonyloxyl quinoxaline derivatives were obtained in moderate to good yields with good functional-group tolerance under mild conditions without additional oxidants. The utility of this methodology and the sulfonyloxyl handles was demonstrated trough gram-scale preparation and the synthesis of 2-substituted quinoxaline-based bioactive molecules, respectively.
The novel C2-O sulfonylation of quinoxalinones
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electro-oxidation induced O-S coupling strategy under mild conditions was reported. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d2cc04524a |