Transition-metal-free four-component reaction of nitriles and disulfides/diselenides

One-pot synthesis of structurally diverse sulfurized/selenated 4-aminopyrimidines has been reported via t -BuOK/K 2 S 2 O 8 -promoted four-component reaction of mixed nitriles and disulfides/diselenides. Mechanistic studies indicate that the reaction proceeds through radical and ionic pathways, and...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2024-01, Vol.6 (7), p.862-865
Hauptverfasser: Wang, Hui-Hui, Zhu, Yang-Yun, Chen, Chuan-Li, Huang, Xiao-Bo, Liu, Miao-Chang, Zhou, Yun-Bing, Wu, Hua-Yue
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Sprache:eng
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Zusammenfassung:One-pot synthesis of structurally diverse sulfurized/selenated 4-aminopyrimidines has been reported via t -BuOK/K 2 S 2 O 8 -promoted four-component reaction of mixed nitriles and disulfides/diselenides. Mechanistic studies indicate that the reaction proceeds through radical and ionic pathways, and an alkenyl sulfide serves as a key intermediate. We have reported t -BuOK/K 2 S 2 O 8 -promoted four-component reaction of mixed nitriles and disulfides/diselenides, providing a one-pot synthetic route to sulfurized/selenated 4-aminopyrimidines.
ISSN:1359-7345
1364-548X
DOI:10.1039/d3cc05416k