Synthesis of Symmetrical Sulfides Enabled by a Sulfur Dioxide Surrogate Acting as a Divalent Sulfur Source

Herein, we present a safe and practical methodology for synthesizing symmetrical sulfides using iodoarenes and potassium metabisulfite (K2S2O5). While K2S2O5 is known as a convenient sulfur dioxide surrogate, here it acts as a divalent sulfur source, pioneering its potential utility. The reaction ex...

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Veröffentlicht in:Organic letters 2022-05, Vol.24 (20), p.3663-3667
Hauptverfasser: Konishi, Hideyuki, Fujita, Ririka, Yamaguchi, Miyuki, Manabe, Kei
Format: Artikel
Sprache:eng
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Zusammenfassung:Herein, we present a safe and practical methodology for synthesizing symmetrical sulfides using iodoarenes and potassium metabisulfite (K2S2O5). While K2S2O5 is known as a convenient sulfur dioxide surrogate, here it acts as a divalent sulfur source, pioneering its potential utility. The reaction exhibits wide substrate generality in which even highly bulky substrates can be applied to afford sterically congested sulfides.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.2c01284