
TY  - JOUR
A1  - Griffiths, PG 
A1  - Moad, G 
A1  - Rizzardo, E 
T1  - Synthesis of the radical scavenger 1,1,3,3-Tetramethylisoindolin-2-yloxyl
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1983
VL  - 36
IS  - 2
SP  - 397
EP  - 401
KW  - 
UR  - https://doi.org/10.1071/CH9830397 
N2  - A versatile free-radical trapping agent, 1,1,3,3-tetramethylisoindolin-2-yloxyl, has been prepared from N-benzylphthalimide by reaction with 'methylmagnesium iodide' in refluxing toluene followed by hydrogenolysis and oxidation. The Grignard reaction gives 2-benzyl-1,1,3,3-tetramethylisoindoline along with a small proportion of an unexpected by-product, 2-benzyl-1-ethyl-1,3,3-trimethyliso-indoline. 
ER  -

