Publication | Closed Access
[2+2]-Photocycloaddition of <i>N</i>-Benzylmaleimide to Alkenes As an Approach to Functional 3-Azabicyclo[3.2.0]heptanes
66
Citations
60
References
2018
Year
EngineeringHeterocyclicPhotochemistryPhotoredox ProcessMedicineSynthetic PhotochemistryOrganic ChemistryOne-step SynthesisChemistryHeterocycle ChemistryPharmacologyAdvanced Building BlocksSynthetic ChemistryBiomolecular EngineeringDrug Discovery
A one-step synthesis of functionalized 3-azabicyclo[3.2.0]heptanes by [2+2]-photochemical intermolecular cycloaddition of N-benzylmaleimide to alkenes was elaborated. The obtained compounds were easily transformed into the bi- and tricyclic analogues of piperidine, morpholine, piperazine, and GABA, which are advanced building blocks for drug discovery.
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