
TY  - JOUR
A1  - Bailey, TS 
A1  - Bremner, JB 
A1  - Pelosi, L 
A1  - Skelton, BW 
A1  - White, AH 
T1  - Synthesis and X-Ray Crystal Structure of 8,9-Dimethoxy-4-methyl-3-phenyl-2,3,5,6-tetrahydropyrrolo[2,1-&#945;]isoquinolinium Iodide
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1995
VL  - 48
IS  - 8
SP  - 1437
EP  - 1445
KW  - 
UR  - https://doi.org/10.1071/CH9951437 
N2  - N-Methylation of 6,7-dimethoxy-1-(2¿-phenylcyclopropyl)-3,4-dihydroisoquinoline (3b) with iodomethane in refluxing acetone gave the modified Cloke rearrangement product, 8,9-dimethoxy-4-methyl-3-phenyl-2,3,5,6-tetrahyropyrrolo[2,1-a] isoquinolinium iodide (5b), a new derivative of the pyrrolo [2,1-a] isoquinoline skeleton, together with the methiodide salt (4b) of (3b). The structure of (5b) was confirmed by X-ray crystallographic analysis. 
ER  -

