Sulfenylation of β-Diketones Using C-H Functionalization Strategy was written by Varun, Begur Vasanthkumar;Gadde, Karthik;Prabhu, Kandikere Ramaiah. And the article was included in Organic Letters in 2015.Reference of 23417-29-0 This article mentions the following:
Sulfenylation of β-diketones is challenging as β-diketones undergo deacylation after sulfenylation in the reaction medium. The sulfenylation of β-diketones without deacylation under metal-free conditions at ambient temperature via a cross dehydrogenative coupling (CDC) strategy is reported. The resultant products can be further manipulated to form α,α-disubstituted β-diketones and pyrazoles. In the experiment, the researchers used many compounds, for example, 6-Methyl-1,3-benzoxazole-2-thiol (cas: 23417-29-0Reference of 23417-29-0).
6-Methyl-1,3-benzoxazole-2-thiol (cas: 23417-29-0) belongs to benzoxazole derivatives. Benzoxazole derivatives have different biological activities. In the past years, numerous benzoxazole derivatives have been synthesised and evaluated for their biological potential.Reference of 23417-29-0
Referemce:
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem