Metal-free efficient thiolation of C(sp) functionalization -generated NHTS for the synthesis of novel sulfenylated 2-aminothiazole and imidazothiazole

A direct metal-free approach for the synthesis of novel sulfenylated 2-aminothiazole and imidazothiazole derivatives at room temperature is reported via an in situ -generated electrophilic thiolating agent. The present protocol provides mild and selective access for the insertion of C-S bond functio...

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Veröffentlicht in:New journal of chemistry 2021-03, Vol.45 (1), p.4632-4637
Hauptverfasser: Kadam, Shuddhodan N, Ambhore, Ajay N, Kamble, Rahul D, Wakhradkar, Mahesh G, Gavhane, Priya D, Gaikwad, Milind V, Gunturu, Krishna Chaitanya, Dawane, Bhaskar S
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Zusammenfassung:A direct metal-free approach for the synthesis of novel sulfenylated 2-aminothiazole and imidazothiazole derivatives at room temperature is reported via an in situ -generated electrophilic thiolating agent. The present protocol provides mild and selective access for the insertion of C-S bond functionalization with good yield. The mechanistic path was justified via density functional theory (DFT) calculations, which explore the role of the solvent in the reaction mechanism. A direct metal-free approach for the synthesis of novel sulfenylated 2-aminothiazole and imidazothiazole derivatives at room temperature is reported via an in situ -generated electrophilic thiolating agent.
ISSN:1144-0546
1369-9261
DOI:10.1039/d0nj05904h