
TY  - JOUR
A1  - Black, DSC 
A1  - Johnstone, LM 
T1  - Nitrones and oxaziridines. XXXII. Some reactions of bicyclic 1-pyrroline 1-oxides
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1984
VL  - 37
IS  - 3
SP  - 577
EP  - 585
KW  - 
UR  - https://doi.org/10.1071/CH9840577 
N2  - Oxidation of the bicyclic nitrone (2) with nitric acid gave the nitro diketone (3). Bridgehead hydroxylation was achieved by conversion of the nitrones (1), (2) and (8) into the imino-benzoates (4), (5) and (9) respectively with benzoyl chloride and subsequent base hydrolysis to give the hydroxy-imines (6), (7) and (10) respectively. Photoirradiation of the bicyclic nitrone (2) gave the oxaziridine (14), which on further irradiation gave the fused azetidine (15) and the fused pyrroline (16). 
ER  -

