MAHBOOBI, S and KARCHER, A and GROTHUS, G and WAGNER, W and WIEGREBE, W (1994) REMOVAL OF THE PYRROLIDINE SUBSTITUENT BY DEHYDROGENATION OF 4-PYRROLIDIN-2-YL-3,4-DIHYDRO-TETRAHYDROISOQUINOLINE AND 1,2,3,4-TETRAHYDROISOQUINOLINE. ARCHIV DER PHARMAZIE, 327 (7). pp. 417-428. ISSN 0365-6233, 1521-4184
Full text not available from this repository.Abstract
Pyrrolidin-2-yl-groups located at C-4 of 3,4-dihydro- or 1,2,3,4-tetrahydroisoquinolines, respectively, are lost in the course of dehydrogenation of these isoquinoline derivatives. However, acyclically substituted isoquinolines, hydrogenated in ring B, 2-benzyl-4-(1-dimethylaminoethyl)-1,2,3,4-tetrahydroisoquinoline, e.g., show loss of the amine group only by benzylic cleavage, affording 4-ethylisoquinoline. Scope and limitation of this reaction are determined using specifically substituted isoquinolines.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | ; |
| Depositing User: | Dr. Gernot Deinzer |
| Last Modified: | 19 Oct 2022 08:40 |
| URI: | https://pred.uni-regensburg.de/id/eprint/53204 |
Actions (login required)
 |
View Item |
