Search results for "Bischler-Napieralski cyclodehydration"

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Synthesis of new antimicrobial pyrrolo[2,1-a]isoquinolin-3-ones

2012

The attractive structure of the pyrroloisoquinoline moiety, together with its potential antimicrobial activity, encouraged us to prepare six 8-substituted and seven 8,9-disubstituted-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinolin-3-ones in a few steps with good yields. We applied a convenient methodology via double intramolecular cyclization conducted by a Bischler-Napieralski cyclodehydration-imine reduction sequence, which is widely employed in the synthesis of isoquinoline alkaloids. Therefore, we synthesized three series of these pyrrolo[2,1-a]isoquinolin-3-ones characterized by the substituent at the 8-position or 8,9-positions of the aromatic ring: (a) different side chains are atta…

StereochemistryFungicideClinical BiochemistrySubstituentPharmaceutical ScienceMicrobial Sensitivity TestsRing (chemistry)Gram-Positive BacteriaBiochemistrychemistry.chemical_compoundStructure-Activity RelationshipQUIMICA ORGANICAAnti-Infective AgentsBischler-Napieralski cyclodehydrationGroup (periodic table)Drug DiscoveryGram-Negative BacteriaSide chainStructure–activity relationshipMoietyPyrrolesBactericideIsoquinolineMolecular BiologyChemistryOrganic ChemistryFungiAntimicrobialIsoquinolinesPyrrolo[21-a]isoquinolin-3-onesMolecular Medicine
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