
TY  - JOUR
A1  - Evans, DD 
A1  - Weale, J 
A1  - Weyell, DJ 
T1  - Synthesis of some tricyclic amines&#8211;Hexahydro-1H-indenoazepines and a Hexahydro-1H-benzo-quinoline and -isoquinoline
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1973
VL  - 26
IS  - 6
SP  - 1333
EP  - 1336
KW  - 
UR  - https://doi.org/10.1071/CH9731333 
N2  - 2,3,4,4a,5,6-Hexahydro-1H-indeno[7,1-cd]azepine (6), 2,3,3a,4,5,6- hexahydro-1H-benzo[de]quinoline (10), 2,3,3a,4,5,6-hexahydro-1H- benz[de]isoquinoline (12), isolated as their hydrochlorides, and 2,3,4,4a,5,6-hexahydro-1H-indeno[7,1-bc]azepine (8) have been prepared by lithium aluminium hydride reduction of the corresponding lactams which were synthesized from the appropriate tricyclic ketones by Beckmann rearrangement or Schmidt reaction. The base (8) was also synthesized from 1,2,3,4-tetrahydronaphthalene-1,8-dimethanol (15). 
ER  -

