
TY  - JOUR
A1  - Prager, RH 
A1  - Raner, KD 
A1  - Ward, AD 
T1  - The rearrangements of the nitrones of simple cyclic conjugated ketones
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1984
VL  - 37
IS  - 2
SP  - 381
EP  - 387
KW  - 
UR  - https://doi.org/10.1071/CH9840381 
N2  - The ring expansions of N-methyl nitrones formed from cyclic conjugated ketones have been investigated.  Low yields of cyclic amides were obtained. In general, the best conditions for the rearrangementinvolved using p-toluenesulfonyl chloride and polyphosphoric acid in tetrahydrofuran. The parent ketone and, in some cases, an N-aryl sulfonamide were also obtained; mechanisms for their formation are discussed. 
ER  -

