Publication | Closed Access
Efficient Synthesis of Fused Oxazepino-isoquinoline Scaffolds via an Ugi, Followed by an Intramolecular Cyclization
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Citations
37
References
2017
Year
Combinatorial ChemistryBioorganic ChemistryOrganic ChemistryEfficient SynthesisChemistryHeterocycle ChemistryMedicinal ChemistryOxazepino-isoquinoline ScaffoldsPurification StepIntramolecular CyclizationBiochemistryMicrowave Irradiation ConditionsPharmacologyNatural Product SynthesisHeterocyclicNatural SciencesActive ScaffoldsMedicineSynthetic ChemistryDrug Discovery
A mild and efficient protocol was developed for the synthesis of oxazepino-isoquinolines via a one-pot Ugi four-component reaction, followed by the intramolecular addition of the resulting alcohol to an alkyne moiety under microwave irradiation conditions. Notably, this process only required one purification step, providing facile access to two series of complex and potentially interesting biologically active scaffolds.
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