113345-68-9Relevant academic research and scientific papers
Electrochemical Oxidation of 1-Phenylthio-1-trimethylsilylalkanes
Yoshida, Jun-ichi,Isoe, Sachihiko
, p. 631 - 634 (1987)
Electrochemical oxidation of 1-phenylthio-1-trimethylsilylalkanes in the presence of alcohol resulted in facile cleavage of the carbon-silicon bond and formation of the corresponding acetals.
New one carbon homologation reagents utilizing electrochemical oxidation of organosilicon compounds
Yoshida,Matsunaga,Murata,Isoe
, p. 615 - 624 (2007/10/02)
Phenylthio(trimethylsilyl)methane, phenylthiobis(trimethylsilyl)methane, methoxy(trimethylsilyl)-methane, and methoxybis(trimethylsilyl)methane are deprotonated and the resulting anions are alkylated with electrophiles such as organic halides. The alkylation products are readily converted into the corresponding dimethyl acetals or methyl esters by electrochemical oxidation in methanol.
