198077-47-3Relevant academic research and scientific papers
O -Iodoxybenzoic Acid (IBX)-Iodine Mediated One-Pot Deacylative Sulfonylation of 1,3-Dicarbonyl Compounds: A Synthesis of β-Carbonyl Sulfones
Katrun, Praewpan,Songsichan, Teerawat,Soorukram, Darunee,Pohmakotr, Manat,Reutrakul, Vichai,Kuhakarn, Chutima
supporting information, p. 1109 - 1121 (2017/02/24)
A combination of o-iodoxybenzoic acid (IBX) and a catalytic amount of iodine is found to promote a facile one-pot deacylative sulfonylation reaction of 1,3-dicarbonyl compounds with sodium sulfinates to yield β-carbonyl sulfones. The present method provides the target products bearing a wide variety of functional groups in one step and in good yields.
An efficient electrochemical synthesis of β-keto sulfones from sulfinates and 1,3-dicarbonyl compounds
Pan, Xiao-Jun,Gao, Jian,Yuan, Gao-Qing
, p. 5525 - 5530 (2015/08/03)
An efficient electrochemical synthesis of β-keto sulfones from sulfinates and 1,3-dicarbonyl compounds has been developed. The present electrochemical route could afford the target products in high to excellent yields under mild conditions.
Spectroscopic and theoretical studies of some N,N-diethyl-2-[(4′- substituted)phenylsulfonyl]acetamides
Vinhato, Elisangela,Olivato, Paulo R.,Rodrigues, Alessandro,Zukerman-Schpector, Julio,Colle, Maurizio Dal
experimental part, p. 97 - 106 (2011/11/05)
The analysis of the IR carbonyl band of the N,N-diethyl-2-[(4′- substituted)phenylsulfonyl]acetamides Et2NC(O)CH2S(O) 2C6H4Y (Y = OMe 1, Me 2, H 3, Cl 4, Br 5, NO2 6) supported by B3LYP/6-3
