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Math @ Duke
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Publications [#363558] of Sayan Mukherjee
Papers Published
- Mukherjee, S; Pramanik, A, Mild and Expeditious Synthesis of Sulfenyl Enaminones of l -α-Amino Esters and Aryl/Alkyl Amines through NCS-Mediated Sulfenylation,
ACS Omega, vol. 6 no. 49
(December, 2021),
pp. 33805-33821 [doi]
(last updated on 2025/04/11)
Abstract: Sulfenylation or selenylation of enaminones of l-α-amino esters requires mild reaction conditions due to the presence of a racemization-prone chiral center and reactive side chains. An N-chlorosuccinimide (NCS)-mediated methodology has been developed for rapid sulfenylation of enaminones of l-α-amino esters and aryl/alkyl amines at room temperature in open air under metal-free conditions. Enaminones of l-α-amino esters bearing aliphatic, aromatic, and heterocyclic side chains react efficiently with diverse aryl/alkyl/heteroaryl thiols (R1SH) in the presence of NCS to afford a library of biologically important sulfenyl enaminones in good-to-excellent yields (71-90%). Under similar reaction conditions, the enaminones also react with benzeneselenol to produce selenyl enaminones in good yield (73-83%). The NCS-mediated pathway generates sulfenyl chloride (R1SCl) as an intermediate which leads to rapid sulfenylation of enaminones through cross-dehydrogenative coupling (CDC) under mild reaction conditions.
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