Synthesis of C-3 halogene-substituted apocodeines and apomorphines

Article abstract of DOI:10.1080/00397919108021590

A new effective method has been elaborated for the preparation of the hitherto unknown C-3 halogene derivatives (Cl, Br) of apocodeine and apomorphine, as well as of their N-demethyl-N-substituted (N-propyl, N-alkyl) analogues. These compounds are expected to possess an effect on the dopamine receptor system.

Full text of DOI:10.1080/00397919108021590

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Synthesis of C-3 Halogene-
Substituted Apocodeines and
Apomorphines
Csaba Simon a , Sándor Hosztafi a , Sándor
Makleit b & Sándor Berényi b
a Alkaloida Chemical Factory , Tiszavasvári,
H-4440
b Department of Organic Chemistry , Kossuth
Lajos University , P.O. Box 20, H-4010,
Debrecen, Hungary
Published online: 23 Sep 2006.
To cite this article: Csaba Simon , Sándor Hosztafi , Sándor Makleit & Sándor
Berényi (1991) Synthesis of C-3 Halogene-Substituted Apocodeines and
Apomorphines, Synthetic Communications: An International Journal for Rapid
Communication of Synthetic Organic Chemistry, 21:22, 2309-2316, DOI:
10.1080/00397919108021590
To link to this article: http://dx.doi.org/10.1080/00397919108021590
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