Conversion of aryl iodides into aryliodine(III) dichlorides by an oxidative halogenation strategy using 30% aqueous hydrogen peroxide in fluorinated alcohol.

scientific article published on 20 April 2010

Conversion of aryl iodides into aryliodine(III) dichlorides by an oxidative halogenation strategy using 30% aqueous hydrogen peroxide in fluorinated alcohol. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.3390/MOLECULES15042857
P932PMC publication ID6257259
P698PubMed publication ID20428084
P5875ResearchGate publication ID43352095

P50authorJernej IskraQ43081373
P2093author name stringAjda Podgorsek
P2860cites workElectrophilic aromatic chlorination and haloperoxidation of chloride catalyzed by polyfluorinated alcohols: a new manifestation of template catalysisQ79100775
Chemistry of polyvalent iodineQ37318116
Hypervalent iodine chemistry in synthesis: scope and new directionsQ40430875
Oxidative halogenation with "green" oxidants: oxygen and hydrogen peroxideQ43261863
Synthesis of alkenyldiarylmethane (ADAM) non-nucleoside HIV-1 reverse transcriptase inhibitors with non-identical aromatic ringsQ43821541
Synthesis and reactivity of fluorous and nonfluorous aryl and alkyl iodine(III) dichlorides: new chlorinating reagents that are easily recycled using biphasic protocolsQ46075388
Hypervalent Iodine Goes CatalyticQ60368668
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue4
P407language of work or nameEnglishQ1860
P304page(s)2857-2871
P577publication date2010-04-20
P1433published inMoleculesQ151332
P1476titleConversion of aryl iodides into aryliodine(III) dichlorides by an oxidative halogenation strategy using 30% aqueous hydrogen peroxide in fluorinated alcohol
P478volume15

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Q37353359Catalytic, Stereoselective Dihalogenation of Alkenes: Challenges and Opportunitiescites workP2860

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