| Literature DB >> 20160840 |
Jonathan D Rosen1, Nadezhda German, Robert J Kerns.
Abstract
An optimized total synthesis of the 2-amino-6-chloro-4-cyclopropyl-7-fluoro-5-methoxy-pyrido[1,2-c]pyrimidine-1,3-dione core structure of a new fluoroquinolone-like class of antibacterial agents is described. This synthesis is highlighted by a nearly quantitative ring-closing reaction to form the pyrido[1,2-c]pyrimidine core. This bicyclic ring system serves as a scaffold for a family of biologically active compounds.Entities:
Year: 2009 PMID: 20160840 PMCID: PMC2631556 DOI: 10.1016/j.tetlet.2008.11.121
Source DB: PubMed Journal: Tetrahedron Lett ISSN: 0040-4039 Impact factor: 2.415