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Ligand-Enabled Double γ-C(sp<sup>3</sup> )-H Functionalization of Aliphatic Acids: One-Step Synthesis of γ-Arylated γ-Lactones.


ABSTRACT: γ-methylene C(sp3 )-H functionalization of linear free carboxylic acids remains a significant challenge. Here in we report a Pd(II)-catalyzed tandem γ-arylation and γ-lactonization of aliphatic acids enabled by a L,X-type CarboxPyridone ligand. A wide range of γ-arylated γ-lactones are synthesized in a single step from aliphatic acids in moderate to good yield. Arylated lactones can readily be converted into disubstituted tetrahydrofurans, a prominent scaffold amongst bioactive molecules.

SUBMITTER: Hoque ME 

PROVIDER: S-EPMC11221842 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature