Title of article :
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
Author/Authors :
Mathias Lubbe، نويسنده , , Franziska Bendrath، نويسنده , , Tiana Trabhardt، نويسنده , , Alexander Villinger، نويسنده , , Christine Fischer، نويسنده , , Peter Langer، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
10
From page :
5998
To page :
6007
Abstract :
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-bis(methylthio)ketenacetals resulted in the formation of regioisomeric products containing an acyl group located at position 6.
Keywords :
arenes , Cyclizations , silyl enol ethers , Sulfur , Regioselectivity
Journal title :
Tetrahedron
Serial Year :
2013
Journal title :
Tetrahedron
Record number :
1105993
Link To Document :
بازگشت