
TY  - JOUR
A1  - Brown, RFC 
A1  - Irvine, F 
A1  - Smith, RJ 
T1  - The rearrangement of 8-Phenyl-2-quinolyl nitrene at 530&#176;
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1973
VL  - 26
IS  - 10
SP  - 2213
EP  - 2219
KW  - 
UR  - https://doi.org/10.1071/CH9732213 
N2  - 8-Phenyl-2-quinolyl nitrene, generated by pyrolysis of 9- phenyltetrazolo[1,5-a]-quinoline at 530°/0.2 mm, rearranged to form a single product, 7H-pyrido[2,3,4-gh]-phenanthridine (82%). The formation of this product is consistent with rearrangement by ring expansion of 8-phenyl-2-quinolyl nitrene followed by ring contraction to give 8- phenyl-1-isoquinolyl nitrene. 
ER  -

