
TY  - JOUR
A1  - Cameron, DW 
A1  - Samuel, EL 
T1  - Reaction of <I>peri</I>-Aminonaphthoquinones and Dihydroperimidinones with piperidine
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1977
VL  - 30
IS  - 9
SP  - 2081
EP  - 2085
KW  - 
UR  - https://doi.org/10.1071/CH9772081 
N2  - Reaction of methyl-substituted 5-amino-1,4-naphthoquinones with piperidine gave preferentially 3-piperidino derivatives. The corresponding orientation also resulted from amination of the dihydroperimidinone system (1), a slower process. When position 3 of the naphthoquinone was substituted by a methyl group, preferential side-chain amination of that group was observed. 
ER  -

