Stereoselectivity of oxotremorine antagonists containing a chiral pyrrolidine group
- 1 October 1978
- journal article
- Published by Springer Nature in Cellular and Molecular Life Sciences
- Vol. 34 (10) , 1334-1335
- https://doi.org/10.1007/bf01981455
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- The Optical Activity of the Amide Chromophore, I. MO‐Theoretical calculation of the long‐wavelength optical activity of γ‐lactams and of related isoelectronic moleculesHelvetica Chimica Acta, 1975
- Acetylene compounds of potential pharmacological value. XIX. N-(dialkylaminoalkynyl)-substituted succinimides and 2-pyrrolidones as partial cholinergic agonists.1975
- Stereospecificity of oxotremorine antagonistsCellular and Molecular Life Sciences, 1974
- Asymmetrical nonbridgehead nitrogen—IVTetrahedron, 1974
- Conformational analysis of substituted pyrrolidonesBiopolymers, 1973
- N-(t-Aminoalkynyl)-substituted pyrrolidones as oxotremorine antagonistsCellular and Molecular Life Sciences, 1970
- Acetylene compounds of potential pharmacological value. XIV. N-(tert-aminoalkynyl)-substituted succinimides and maleimides. Class of central anticholinergic agentsJournal of Medicinal Chemistry, 1970
- Absolute configuration and parasympathetic action: Pharmacodynamics of enantiomorphic and diastereoisomeric esters of β-methylcholineJournal of Pharmacy and Pharmacology, 1965
- The Absolute Configuration of the C1 Atom in Retronecanone (1-Methyl-7-oxopyrrolizidine)Journal of the American Chemical Society, 1959
- Überführung optisch aktiver α‐Aminocarbonsäuren in optisch aktive Amine mit gleichem KohlenstoffskelettHelvetica Chimica Acta, 1951