Conclusions from NMR on the preferred direction of attack during quaternisation of 1-benzyl-tetrahydroisoquinolines
- 1 January 1980
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 36 (14) , 2157-2159
- https://doi.org/10.1016/0040-4020(80)80109-8
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Quaternization of 1-substituted 2-methyl-6,7-dialkoxy-1,2,3,4-tetrahydroiso - quinolines and demethylation of the quaternary salts using D, T and 14C marking.Tetrahedron Letters, 1971
- Revision of the structures of (+)-tubocurarine chloride and (+)-chondrocurineJournal of the Chemical Society D: Chemical Communications, 1970
- Quaternization of 1,2-disubstituted 6,7-dimethoxy-1,2,3,4-tetrahydroiso-quinolinesTetrahedron Letters, 1968