4.7 Article

Pd(ii)-Catalyzed atroposelective C-H olefination: synthesis of enantioenriched N-aryl peptoid atropisomers

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CHEMICAL COMMUNICATIONS
卷 59, 期 90, 页码 13518-13521

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cc04425d

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In this study, enantioenriched N-aryl peptoid atropisomers were synthesized via Pd(ii)-catalyzed atroposelective C-H olefination using easily accessible l-pyroglutamic acid as the chiral ligand. The obtained optically active N-aryl peptoid atropisomers exhibited high enantioselectivities and useful yields.
Herein, we reported the synthesis of enantioenriched N-aryl peptoid atropisomers via Pd(ii)-catalyzed atroposelective C-H olefination using the easily accessible l-pyroglutamic acid (l-pGlu-OH) as the chiral ligand. A series of optically active N-aryl peptoid atropisomers were obtained in synthetically useful yields with high enantioselectivities.

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