1541-29-3Relevant articles and documents
REGIOSPECIFIC SYNTHESIS OF α-ARYLSULFONOXY KETONES FROM KETONE DERIVATIVES
Hoffman, Robert V.,Carr, C. Sean
, p. 5811 - 5812 (1986)
Isomeric enol ester, enamine, and silyl enol ether derivatives of unsymmetrical ketones are converted regiospecifically to α-arylsulfonoxy ketones with arylsulfonyl peroxides.
A convenient and selective method for preparation of enol acetates from ketones using montmorillonite KSF clay
Kalita, Biswajit,Bezbarua, Maitreyee Sarma,Barua, Nabin C.
, p. 3181 - 3184 (2007/10/03)
The reaction of ketones with stoichiometric amounts of acetic anhydride and Montmorillonite KSF clay at room temperature afforded the corresponding enol acetates in excellent yields. It has also been observed that by performing the reactions under microwave irradiation the reaction time can be dramatically reduced.
A selective catalytic method of enol-acetylation under microwave Irradiation
Kalita, Dipok J.,Borah, Ruli,Sarma, Jadab C.
, p. 404 - 405 (2007/10/03)
Six-membered cyclic ketones on treatment with acetic anhydride and a catalytic amount of iodine under microwave irradiation give the corresponding enol acetates in good yield.
Unprecedented Route to Enolates from Silyl Enol Ethers and Enol Acetates: Reaction with Hard and Soft Electrophiles
Duhamel, Pierre,Cahard, Dominique,Poirier, Jean-Marie
, p. 2509 - 2512 (2007/10/02)
Reaction of silyl enol ethers with lithium, sodium or better, potassium alkoxides resulted in a rapid formation of enolates which were trapped with hard electrophiles and benzaldehyde.Moreover, in the aldolisation reaction, only a catalytic amount of alka
