1383467-84-2Relevant academic research and scientific papers
An aqueous and recyclable copper(i)-catalyzed route to α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols
Watile, Rahul A.,Biswas, Srijit,Samec, Joseph S. M.
supporting information, p. 3176 - 3179 (2013/11/06)
A highly efficient one-step copper(i)-catalyzed method for the synthesis of α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols in aqueous media is described. A variety of α-sulfenylated carbonyl compounds can be synthesized in good to excellent yields. The catalyst has been successfully recycled up to 4 times without any loss of activity in an aqueous medium.
Atom-efficient gold(I)-chloride-catalyzed synthesis of α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols: Substrate scope and experimental and theoretical mechanistic investigation
Biswas, Srijit,Dahlstrand, Christian,Watile, Rahul A.,Kalek, Marcin,Himo, Fahmi,Samec, Joseph S. M.
supporting information, p. 17939 - 17950 (2014/01/17)
Gold(I)-chloride-catalyzed synthesis of α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols showed a wide substrate scope with respect to both propargylic alcohols and aryl thiols. Primary and secondary aromatic propargylic alcohol
A gold(I)-catalyzed route to α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols
Biswas, Srijit,Samec, Joseph S. M.
supporting information; experimental part, p. 6586 - 6588 (2012/07/28)
A one-step atom efficient gold(i)-catalyzed route to α-sulfenylated ketones and aldehydes from propargylic alcohols and aryl thiols is described.
