The thioamidation of -dibromoalkenes in an aqueous medium

The direct integration of sulphur and amine groups with 1,1-dibromoalkenes for thioamide synthesis has been achieved in an aqueous medium. The presented green protocol emphasizes the suitability of aqueous media for the thioamidation reaction and enables greater selectivity with synthetic utility. A...

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Veröffentlicht in:Organic & biomolecular chemistry 2021-03, Vol.19 (11), p.2473-248
Hauptverfasser: Vankar, Jigarkumar K, Gupta, Ankush, Jadav, Jaydeepbhai P, Nanjegowda, Shankara H, Gururaja, Guddeangadi N
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Zusammenfassung:The direct integration of sulphur and amine groups with 1,1-dibromoalkenes for thioamide synthesis has been achieved in an aqueous medium. The presented green protocol emphasizes the suitability of aqueous media for the thioamidation reaction and enables greater selectivity with synthetic utility. A wide range of thioamides in moderate to excellent yields has been achieved using readily available starting materials, with the use of no organic solvents, catalysts, or additives. The direct integration of sulphur and amine groups with 1,1-dibromoalkenes for thioamide synthesis has been achieved in an aqueous medium.
ISSN:1477-0520
1477-0539
DOI:10.1039/d0ob02319a