
TY  - JOUR
A1  - Badger, GM 
A1  - Cheuychit, P 
A1  - Sasse, WHF 
T1  - Synthetical applications of activated metal catalysts. XXIV. The desulphurization of sulphones
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1964
VL  - 17
IS  - 3
SP  - 371
EP  - 374
KW  - 
UR  - https://doi.org/10.1071/CH9640371 
N2  - Diphenylsulphone has been found to be much more resistant to desulphurization than diphenylsulphoxide or diphenylsulphide. The desulphurization of benzo[b]thiophen-3-(carboxylic acid)-1,1-dioxide with Raney cobalt has been found to give benzo[b]thiophen-3-oarboxylic acid, 2-phenylpropionic acid, phenylacetic acid, and a small amount of an unidentified labile acid. The results support the view that the desulphurization of sulphones proceeds via the sulphides. 
ER  -

