Articles with "thianthrenation" as a keyword



Palladium-Catalyzed Synthesis of Esters from Arenes through C-H Thianthrenation.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c02330

Abstract: The efficient palladium-catalyzed synthesis of esters from readily available arenes has been developed. These C-H bond esterifications were achieved relying on the regioselective thianthrenation to generate the aryl-TT salts, which were treated as reactive electrophilic… read more here.

Keywords: catalyzed synthesis; palladium catalyzed; synthesis esters; thianthrenation ... See more keywords

Site-Selective C-H Mono- and Bis-Thianthrenation of Polycyclic Aromatic Hydrocarbons.

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Published in 2025 at "Organic letters"

DOI: 10.1021/acs.orglett.5c02903

Abstract: Organic functional materials are often constructed from polycyclic aromatic hydrocarbons. They contain multiple C-H positions, making site-selective functionalization challenging. We present the highly site-selective thianthrenation of unsubstituted polycyclic aromatic hydrocarbons, giving single regioisomers. The site… read more here.

Keywords: bis thianthrenation; thianthrenation; polycyclic aromatic; site selective ... See more keywords

Cu-Mediated Thianthrenation and Phenoxathiination of Arylborons.

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Published in 2023 at "Journal of the American Chemical Society"

DOI: 10.1021/jacs.3c03413

Abstract: Great success in synthetic chemistry is motivated by the development of novel and reactive linchpins for carbon-carbon and carbon-heteroatom bond formation reactions, which has dramatically altered chemists' approach to building molecules. Herein, we report the… read more here.

Keywords: thianthrenation phenoxathiination; chemistry; phenoxathiination arylborons; mediated thianthrenation ... See more keywords

Unified metal-free intermolecular Heck-type sulfonylation, cyanation, amination, amidation of alkenes by thianthrenation

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Published in 2024 at "Nature Communications"

DOI: 10.1038/s41467-024-44746-w

Abstract: Direct and site-selective C-H functionalization of alkenes under environmentally benign conditions represents a useful and attractive yet challenging transformation to access value-added molecules. Herein, a unified protocol for a variety of intermolecular Heck-type functionalizations of… read more here.

Keywords: metal free; thianthrenation; intermolecular heck; heck type ... See more keywords

Thianthrenation-promoted photoinduced alkene difunctionalization and aryl allylation with Morita-Baylis-Hillman adducts.

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Published in 2024 at "Chemical communications"

DOI: 10.1039/d4cc01792g

Abstract: An organophotoredox-catalyzed alkoxyallylation of feed-stock olefins, through thianthrenation using a Morita-Baylis-Hillman adduct as an allylating agent, is described. Site-selective addition of MeOH to an alkene-thianthrenium salt and its subsequent conversion into a nucleophilic radical species… read more here.

Keywords: aryl allylation; baylis hillman; thianthrenation; morita baylis ... See more keywords