1088703-89-2Relevant academic research and scientific papers
Regioselective synthesis of 3-(methylthio)phenols by formal [3+3]-cyclocondensations of 3-oxo-bis(methylthio)ketenacetals with 1,3-bis(trimethylsilyloxy)-1,3-butadienes and 1,3-dicarbonyl dianions
Lubbe, Mathias,Bendrath, Franziska,Trabhardt, Tiana,Villinger, Alexander,Fischer, Christine,Langer, Peter
, p. 5998 - 6007 (2013/07/25)
The cyclization of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with 3-oxo-bis(methylthio)ketenacetals afforded 3-(methylthio)phenols containing an acyl or ester substituent located at position 2. The cyclization of free 1,3-dicarbonyl dianions with 3-oxo-bi
Regioselective synthesis of functionalized 3-(methylthio)phenols by the first formal [3+3] cyclocondensations of 1,3-bis(trimethylsilyloxy)-1,3- butadienes with 1,1-bis(methylthio)-1-en-3-ones
Lubbe, Mathias,Klassen, Renske,Trabhardt, Tiana,Villinger, Alexander,Langer, Peter
scheme or table, p. 2331 - 2333 (2009/04/11)
The [3+3] cyclocondensation of 1,3-bis(silyl enol ethers) with 1,1-bis(methylthio)-1-en-3-ones results in the regioselective formation of 3-(methylthio)phenols. The products represent useful synthetic building blocks, which are not readily available by ot
