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

Citation
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
Citations number
22
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404020
Volume
50
Issue
7
Year of publication
1994
Pages
2107 - 2114
Database
ISI
SICI code
0040-4020(1994)50:7<2107:RCTA-A>2.0.ZU;2-X
Abstract
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.