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Functionalization of λ<sup>5</sup>-Phosphinines via metalation strategies.


ABSTRACT: Phosphinines, or phosphabenzenes, exhibit distinctive electronic properties yet remain underexplored due to the challenges associated with their selective functionalization. We present herein the straightforward functionalization of λ5-phosphinine derivatives using organometallic strategies. Halogen-zinc and -magnesium exchanges were successfully performed employing Et2Zn·2Oamyl or i-PrMgCl·LiCl species under smooth reaction conditions. Such method allowed access to a wide range of sophisticated architectures, photophysical studies of which demonstrated interesting fluorescence properties. With the possibility of using such fluorescence in biomarking, λ5-phosphinines were grafted on a few glycosides, nucleosides and pharmaceutically relevant moieties.

SUBMITTER: Rambaud F 

PROVIDER: S-EPMC12748612 | biostudies-literature | 2025 Dec

REPOSITORIES: biostudies-literature