RADICAL CYCLIZATION TO APORPHINES - A NEW, EFFICIENT TOTAL SYNTHESIS OF THE APORPHINE GLAUCINE AND THE 4,5-DIOXOAPORPHINE PONTEVEDRINE, ANDTHE FIRST TOTAL SYNTHESIS OF 5-OXOAPORPHINES
Jc. Estevez et al., RADICAL CYCLIZATION TO APORPHINES - A NEW, EFFICIENT TOTAL SYNTHESIS OF THE APORPHINE GLAUCINE AND THE 4,5-DIOXOAPORPHINE PONTEVEDRINE, ANDTHE FIRST TOTAL SYNTHESIS OF 5-OXOAPORPHINES, Tetrahedron, 50(7), 1994, pp. 2107-2114
We describe the radical cyclization of bromobenzylisoquinolines and be
nzylisoquinolin-3-ones, which afford aporphines or the novel 5-oxoapor
phines and 5-oxodehydroaporphines respectively. Oxidation of the latte
r compounds provides a new route to 4,5-dioxoaporphines.