
%0 Journal Article
%A Bailey, TS 
%A Bremner, JB 
%A Pelosi, L 
%A Skelton, BW 
%A White, AH 
%T Synthesis and X-Ray Crystal Structure of 8,9-Dimethoxy-4-methyl-3-phenyl-2,3,5,6-tetrahydropyrrolo[2,1-&#945;]isoquinolinium Iodide
%J Australian Journal of Chemistry
%D 1995/08/01
%V 48
%N 8
%P 1437-1445
%K 
%R https://doi.org/10.1071/CH9951437
%U https://www.publish.csiro.au/paper/CH9951437 
%X 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. 
