Armir Zogu | University of Prishtina (original) (raw)

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Papers by Armir Zogu

Research paper thumbnail of De-risking S–F bond formation: A gas cylinder-free strategy to access S(IV) and S(VI) fluorinated compounds

The sulfur-fluorine partnership occupies a privileged position in fluorine chemistry given the fu... more The sulfur-fluorine partnership occupies a privileged position in fluorine chemistry given the functional versatility that it imparts to organic structures. Despite this, available methodologies to forge S–F bonds are limited compared to C–F bond formation. Here, we describe a synthetic protocol that selectively enables the oxidative halogenation of aliphatic, aromatic, and heteroaromatic thiols to their corresponding SF4Cl, SO2F and SF3 derivatives. Selective oxidation of thiols to either S(IV)–F or S(VI)–F compounds is achieved by employing bench-stable calcium hypochlorite as chlorine surrogate (CLOgen), in the presence of KF as fluoride source. DFT calculations provided insight into the mechanistic aspects of the transformation and rationalized the observed isomeric preference towards the SF4Cl derivatives. Ultimately, this glovebox-free method selectively dispatches three classes of compounds upon reaction condition finetuning. Furthermore, first-in-class transformations are re...

Research paper thumbnail of Frontispiece: Chemistry of Pentafluorosulfanyl Derivatives and Related Analogs: From Synthesis to Applications

Chemistry – A European Journal

Research paper thumbnail of Chemistry of Pentafluorosulfanyl Derivatives and Related Analogs: From Synthesis to Applications

Chemistry – A European Journal

Research paper thumbnail of De‐risking S‐F bond formation:A gas cylinder‐free strategy to access S(IV) and S(VI) fluorinated compounds

Chemistry – A European Journal

Research paper thumbnail of Sn

Research paper thumbnail of De-risking S–F bond formation: A gas cylinder-free strategy to access S(IV) and S(VI) fluorinated compounds

The sulfur-fluorine partnership occupies a privileged position in fluorine chemistry given the fu... more The sulfur-fluorine partnership occupies a privileged position in fluorine chemistry given the functional versatility that it imparts to organic structures. Despite this, available methodologies to forge S–F bonds are limited compared to C–F bond formation. Here, we describe a synthetic protocol that selectively enables the oxidative halogenation of aliphatic, aromatic, and heteroaromatic thiols to their corresponding SF4Cl, SO2F and SF3 derivatives. Selective oxidation of thiols to either S(IV)–F or S(VI)–F compounds is achieved by employing bench-stable calcium hypochlorite as chlorine surrogate (CLOgen), in the presence of KF as fluoride source. DFT calculations provided insight into the mechanistic aspects of the transformation and rationalized the observed isomeric preference towards the SF4Cl derivatives. Ultimately, this glovebox-free method selectively dispatches three classes of compounds upon reaction condition finetuning. Furthermore, first-in-class transformations are re...

Research paper thumbnail of Frontispiece: Chemistry of Pentafluorosulfanyl Derivatives and Related Analogs: From Synthesis to Applications

Chemistry – A European Journal

Research paper thumbnail of Chemistry of Pentafluorosulfanyl Derivatives and Related Analogs: From Synthesis to Applications

Chemistry – A European Journal

Research paper thumbnail of De‐risking S‐F bond formation:A gas cylinder‐free strategy to access S(IV) and S(VI) fluorinated compounds

Chemistry – A European Journal

Research paper thumbnail of Sn

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