Design and pharmacology of quinuclidine derivatives as M2-selective muscarinic receptor ligands

Design and pharmacology of quinuclidine derivatives as M2-selective muscarinic receptor ligands Muscarinic agonist, (±)-quinuclidin-3-yl-(4-fluorophenethyl)(phenyl)carbamate: High affinity, but low subtype selectivity for human M1 – M5 muscarinic acetylcholine receptors Synthesis of some 3-(1-azabicyclo[2.2.2]octyl) 3-amino-2-hydroxy-2-phenylpropionates: profile of antimuscarinic efficacy and selectivity Structure−Activity Relationships of Dimethindene Derivatives as New M₂-Selective Muscarinic Receptor Antagonists Antimuscarinic 3-(2-Furanyl)quinuclidin-2-ene Derivatives:  Synthesis and Structure−Activity Relationships Affinity and selectivity of the optical isomers of 3-quinuclidinyl benzilate and related muscarinic antagonists Novel quinuclidine-based ligands for the muscarinic cholinergic receptor Synthesis and muscarinic activity of quinuclidinyl- and (1-azanorbornyl)pyrazine derivatives Synthesis and muscarinic receptor activity of ester derivatives of 2-substituted 2-azabicyclo[2.2.1]heptan-5-ol and -6-ol Analogs of 3-quinuclidinyl benzilate