Photocatalysis and Kinetic Resolution by Lithiation to Give Enantioenriched 2-Arylpiperazines.

Org Lett

Department of Chemistry, University of Sheffield, Brook Hill, Sheffield S3 7HF, U.K.

Published: February 2023

Piperazines are important heterocycles in drug compounds. We report the asymmetric synthesis of arylpiperazines by photocatalytic decarboxylative arylation (metallaphotoredox catalysis) then kinetic resolution using -BuLi/(+)-sparteine. This gave a range of piperazines with very high enantioselectivities. Further functionalizations gave enantioenriched 2,2-disubstituted piperazines, and either N-substituent can be removed selectively. Late-stage functionalizations of enantioenriched piperazine derivatives were demonstrated, including synthesis of a drug compound with glycogen synthase kinase (GSK)-3β inhibitor activity with potential for treating Alzheimer's disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9942196PMC
http://dx.doi.org/10.1021/acs.orglett.3c00074DOI Listing

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