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 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
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. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d3cc05416k |