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Org Biomol Chem ; 21(22): 4591-4595, 2023 Jun 07.
Article in English | MEDLINE | ID: mdl-37203457

ABSTRACT

Fragment-based lead discovery (FBLD) often relies on flat, aromatic compounds which display undesirable physicochemical properties with limited exit vectors for fragment growth. Herein, we report concise synthetic strategies to sp3-rich heterocyclic fragments encompassing polar exit vectors poised for fragment-to-lead (F2L) development.

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