23,99 €
inkl. MwSt.
Versandfertig in 6-10 Tagen
12 °P sammeln
Andere Kunden interessierten sich auch für
![Energy efficient Synthesis of 5-substituted phenyl-3H-chromeno]( "Energy efficient Synthesis of 5-substituted phenyl-3H-chromeno")
Energy efficient Synthesis of 5-substituted phenyl-3H-chromeno36,99 €![Synthesis of Pyrazoles: A Simple, Convenient and Efficient Approach]( "Synthesis of Pyrazoles: A Simple, Convenient and Efficient Approach")
Synthesis of Pyrazoles: A Simple, Convenient and Efficient Approach51,99 €![Development of Method for the Synthesis of Bioactive Heterocycles]( "Development of Method for the Synthesis of Bioactive Heterocycles")
Development of Method for the Synthesis of Bioactive Heterocycles36,99 €![New Avenues to Efficient Chemical Synthesis]( "New Avenues to Efficient Chemical Synthesis")
New Avenues to Efficient Chemical Synthesis74,99 €![Studies on Post Heterocyclization of THTPs]( "Studies on Post Heterocyclization of THTPs")
Studies on Post Heterocyclization of THTPs44,99 €![Studies on Chemical Synthesis of Peptides: Efficient Synthetic Methods for ¿-Amino Acids, Azides, Amino Acid Hydroxamates and Esters]( "Studies on Chemical Synthesis of Peptides: Efficient Synthetic Methods for ¿-Amino Acids, Azides, Amino Acid Hydroxamates and Esters")
Studies on Chemical Synthesis of Peptides: Efficient Synthetic Methods for ¿-Amino Acids, Azides, Amino Acid Hydroxamates and Esters52,95 €![Synthesis and Biological activities of some Heterocyclics]( "Synthesis and Biological activities of some Heterocyclics")
Synthesis and Biological activities of some Heterocyclics36,99 €
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.