Efficient Method for the Synthesis of Novel Oxazinoquinolinones

Pyranoquinoline skeletons including both a quinoline ring and a pyran moiety, afford exceptional biological activities.Rings annulated to the pyranoquinolinone units showed potential medicinal properties such as antibacterial, anticoagulant, antitumor,and microtubule targeting agents. Despite the extensive body of published work on the synthesis of this type of compounds, we are not aware of any report that describes a simple procedure for the annulation of an oxazole and /or oxazino nucleus to the pyranoquinolinone moiety to give a tetracyclic system. Oxazole and/ or oxazino derivatives have been found in numerous natural products and many of them have been shown to have an interesting broad range of biological activities, such as in inhibition of Streptococcus mutans biofilm formation,antipsychotics, HIV inhibitory, and anti-tumoral activities.

Autorentext

Mohamed Hassan graduated from Ain Shams University with a BSc (Hons) and PhD after several scientific awards in organic chemistry departments all overt the world(Slovakia and Italy ) before his appointment as visitor scholarship Fellow at the Australian national university(Australia) as a good expert in synthetic organic chemistry.