314769-46-5Relevant academic research and scientific papers
Regioselective synthesis of diaryl sulfides by [3+3] cyclizations of 1,3-bis(trimethylsilyloxy)-1,3-dienes
Rashid, Muhammad A.,Reinke, Helmut,Langer, Peter
, p. 2321 - 2323 (2007)
Functionalized and sterically encumbered diaryl sulfides were prepared based on [3+3] cyclizations of 1,3-bis(trimethylsilyloxy)-1,3-dienes.
A Green Mechanochemical Synthesis of New 3,5-Dimethyl-4-(arylsulfanyl)pyrazoles
Saeed, Aamer,Channar, Pervaiz Ali
, p. 780 - 783 (2017/02/03)
A small series of new 3,5-dimethyl-4-(arylsulfanyl)pyrazoles have been synthesized in good to excellent yields by a grinding-induced, sequential one-pot three-component reaction, of an equimolar mixture of 3-chloro-2,4-pentanedione, differently substitute
K2S2O8/I2 promoted syntheses of α-thio-β-dicarbonyl compounds via oxidative C-S coupling reactions under transition metal-free and solvent-free conditions
Liu, Yi-Wei,Badsara, Satpal Singh,Liu, Yi-Chen,Lee, Chin-Fa
, p. 44299 - 44305 (2015/06/02)
A K2S2O8/I2 promoted C-S coupling reaction of β-diketones with disulfides has been described. The resulting α-thio-β-diketone compounds were obtained in good to excellent yields. Both diaryl and dialkyl disulfid
Synthesis of functionalized diaryl sulfides based on regioselective one-pot cyclizations of 1,3-bis(trimethylsilyloxy)-1,3-butadienes
Rashid, Muhammad A.,Rasool, Nasir,Adeel, Muhammad,Reinke, Helmut,Fischer, Christine,Langer, Peter
, p. 3782 - 3793 (2008/09/20)
Functionalized diaryl sulfides were prepared based on one-pot cyclizations of 1,3-bis(trimethylsilyloxy)-1,3-butadienes.
