39601-01-9Relevant academic research and scientific papers
Generation and reactions of thiirenium ions by the Cation Pool method
Shimizu, Akihiro,Horiuchi, Shun,Hayashi, Ryutaro,Matsumoto, Kouichi,Miyamoto, Yu,Morisawa, Yusuke,Wakabayashi, Tomonari,Yoshida, Jun-Ichi
, p. 97 - 113 (2017)
Thiirenium ions generated and accumulated by low-temperature electrochemical oxidation of disulfides in the presence of alkynes were successfully observed by low-temperature NMR, Raman, and mass spectroscopies and were found to be stable at temperatures below -40 °C. The thiirenium ions showed ambident reactivity toward subsequently added nucleophiles to give either disubstituted alkenes or alkynes depending on the nature of the nucleophiles.
Electrophilic Addition of 4'-Nitrobenzenesulphenanilide to Alkynes in Acetic Acid. A Synthesis of β-Acetoxyvinyl Sulphides
Benati, Luisa,Casarini, Daniele,Montevecchi, Pier Carlo,Spagnolo, Piero
, p. 1113 - 1116 (2007/10/02)
4'-Nitrobenzenesulphenanilide reacts at room temperature with simple alkyl- and aryl-alkynes in acetic acid in the presence of boron trifluoride-diethyl ether to afford products of acetoxysulphenylation in moderate to good yields.The addition products are
A CONVENIENT SYNTHESIS OF Β-KETO PHENYL SULPHIDES FROM ALKYNES.
Benati, L.,Montevecchi, P.C.,Spagnolo, P.
, p. 2381 - 2384 (2007/10/02)
β-Keto sulphides can be conveniently prepared by BF3-promoted reaction of 4'-nitrobenzenesulphenanilide in acetonitrile or acetic acid and subsequent hydrolysis of the resulting β-acetamidino- or β-acetoxy-vinyl phenyl sulphides.
