113345-65-6Relevant academic research and scientific papers
An alternative route to protected aldols: Cobalt-catalyzed hydroformylation of epoxides and in situ protection of β-hydroxyaldehydes by HC(OMe) 3
Nakano, Koji,Katayama, Masaya,Ishihara, Shinjiro,Hiyama, Tamejiro,Nozaki, Kyoko
, p. 1367 - 1370 (2004)
A wide range of epoxides were efficiently converted to protected aldols by hydroformylation-acetalization using Co2(CO)8 as a catalyst in trimethyl orthoformate. The formylation of terminal epoxides was regioselective for the terminal position, and (S)-1-benzyloxy-2,3-epoxypropane was transformed into (R)-1-benzyloxy-4,4-dimethoxybutan-2-ol with retention of the configuration.
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.
Electrochemical Oxidation of 1-Phenylthio-1-trimethylsilylalkanes
Yoshida, Jun-ichi,Isoe, Sachihiko
, p. 631 - 634 (2007/10/02)
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.
