Short and efficient syntheses of analogues of way-100635: new and potent 5-HT1A receptor antagonists
- 1 March 2001
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry
- Vol. 9 (3) , 695-702
- https://doi.org/10.1016/s0968-0896(00)00287-x
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- An Efficient Synthesis of (Fluoromethyl)pyridylamines for Labeling with Fluorine-18The Journal of Organic Chemistry, 1999
- Linear and macrocyclic ligands containing alternating pyridine and imidazolidin-2-one units 1Journal of the Chemical Society, Perkin Transactions 1, 1998
- Structure−Activity Relationships for the Binding of Arylpiperazines and Arylbiguanides at 5-HT3Serotonin ReceptorsJournal of Medicinal Chemistry, 1996
- First delineation of 5-HT1A receptors in human brain with PET and [11C]WAY-100635European Journal of Pharmacology, 1995
- New (2-Methoxyphenyl)piperazine Derivatives as 5-HT1A Receptor Ligands with Reduced .alpha.1-Adrenergic Activity. Synthesis and Structure-Affinity RelationshipsJournal of Medicinal Chemistry, 1995
- Regioselective Monobromination of Aromatic Amines with Tetrabutylammonium TribromideSynthetic Communications, 1986
- Preparation of 2‐fluoroquinoline and 2,6‐difluoropyridine by halogen exchangeRecueil des Travaux Chimiques des Pays-Bas, 1962
- A new synthesis of 2,6‐dibromopyridine‐N‐oxideRecueil des Travaux Chimiques des Pays-Bas, 1959
- 33. The structure and reactivity of 2-aminopyridine 1-oxideJournal of the Chemical Society, 1957
- The chlorination of pyridine: Investigations on pyridine and quinoline derivatives 41st. CommunicationRecueil des Travaux Chimiques des Pays-Bas, 1939