| Title : Stereoselectivity of oxotremorine antagonists containing a chiral pyrrolidine group - Ringdahl_1978_Experientia_34_1334 |
| Author(s) : Ringdahl B , Dahlbom R |
| Ref : Experientia , 34 :1334 , 1978 |
|
Abstract :
Oxotremorine (Ia) and its succinimide analogue (IIa) have been substituted in the pyrrolidine ring with a methyl group in the 2- or 3-positions. The compounds are oxotremorine antagonists. The 2-methyl-substituted enantiomers show stereoselectivity, the S-isomers being the most active. |
| PubMedSearch : Ringdahl_1978_Experientia_34_1334 |
| PubMedID: 738410 |
Ringdahl B, Dahlbom R (1978)
Stereoselectivity of oxotremorine antagonists containing a chiral pyrrolidine group
Experientia
34 :1334
Ringdahl B, Dahlbom R (1978)
Experientia
34 :1334