Publication | Closed Access
One-Pot Enantioselective Synthesis of Functionalized Pyranocoumarins and 2-Amino-4<i>H</i>-chromenes: Discovery of a Type of Potent Antibacterial Agent
210
Citations
54
References
2011
Year
Combinatorial ChemistryBioorganic ChemistryOrganic ChemistryFunction-oriented DesignChemistryHeterocycle ChemistryPharmaceutical ChemistrySmall MoleculesFunctionalized PyranocoumarinsMedicinal ChemistryHuman PathogensPotent Antibacterial AgentBiochemistryDiversity-oriented SynthesisNatural Product SynthesisPharmacologyChiral Small MoleculesEnantioselective SynthesisNatural SciencesMedicineSynthetic ChemistryOne-pot Enantioselective SynthesisDrug Discovery
Function-oriented design and synthesis of chiral small molecules with novel activity is a key goal in modern organic chemistry. As multiple antibiotic-resistant pathogens are emerging and causing serious diseases, the need for practical routes for the development of new types of antibacterial agents is very urgent. Herein, we present a highly efficient process for the synthesis of optically active pyranocoumarins and 2-amino-4H-chromenes through an organocatalytic Knoevenagel/Michael/cyclization sequence, and the preliminary biological studies of these new heterocyclic compounds revealed potent antibacterial activity. This study provides a novel strategy for further research and development of new types of antibacterial agents effective against human pathogens.
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