Friedländer reaction on 2-amino-3-cyano-4H-pyrans: Synthesis of derivatives of 4H-pyran [2,3-b] quinoline, new tacrine analogues
- 1 December 1997
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 7 (24) , 3165-3170
- https://doi.org/10.1016/s0960-894x(97)10165-2
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Convenient synthesis of amino-substituted pyranopyranonesTetrahedron Letters, 1997
- Discovery of Novel, Non-Peptide HIV-1 Protease Inhibitors by Pharmacophore SearchingJournal of Medicinal Chemistry, 1996
- First asymmetric synthesis of 3-alkoxycarbonyl-2-amino-4-aryl-4H-naphtho[1,2-b]pyransJournal of Heterocyclic Chemistry, 1996
- Synthesis and evaluation of tacrine-related compounds for the treatment of Alzheimer's diseaseEuropean Journal of Medicinal Chemistry, 1994
- Tacrine: First Drug Approved for Alzheimer's DiseaseAnnals of Pharmacotherapy, 1994
- Drug development for senile cognitive declineJournal of Medicinal Chemistry, 1986
- 13C NMR spectra of 2‐amino‐4H‐pyran derivativesMagnetic Resonance in Chemistry, 1985
- Synthesis of heterocyclic compounds VII. 6-amino-2,4-diaryl-3,5-dicyano-4H-pyransTetrahedron Letters, 1977