1 article(s) from Pradhan, Suman
An overview of different chiral iodine reagents or precursors thereof.
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Asymmetric oxidation of sulfides by chiral hypervalent iodine reagents.
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Oxidative dearomatization of naphthol derivatives by Kita et al.
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[4 + 2] Diels–Alder dimerization reported by Birman et al.
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m-CPBA guided catalytic oxidative naphthol dearomatization.
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Oxidative dearomatization of phenolic derivatives by Ishihara et al.
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Oxidative spirocyclization applying precatalyst 11 developed by Ciufolini et al.
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Asymmetric hydroxylative dearomatization.
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Enantioselective oxylactonization reported by Fujita et al.
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Dioxytosylation of styrene (47) by Wirth et al.
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Oxyarylation and aminoarylation of alkenes.
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Asymmetric diamination of alkenes.
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Stereoselective oxyamination of alkenes reported by Wirth et al.
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Enantioselective and regioselective aminofluorination by Nevado et al.
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Fluorinated difunctionalization reported by Jacobsen et al.
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Aryl rearrangement reported by Wirth et al.
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α-Arylation of β-ketoesters.
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Asymmetric α-oxytosylation of carbonyls.
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Asymmetric α-oxygenation and α-amination of carbonyls reported by Wirth et al.
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Asymmetric α-functionalization of ketophenols using chiral quaternary ammonium (hypo)iodite salt re...
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Oxidative Intramolecular coupling by Gong et al.
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α-Sulfonyl and α-phosphoryl oxylation of ketones reported by Masson et al.
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α-Fluorination of β-keto esters.
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Alkynylation of β-ketoesters and amides catalyzed by phase-transfer catalyst.
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Alkynylation of β-ketoesters and dearomative alkynylation of phenols.
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Beilstein J. Org. Chem. 2018, 14, 1244–1262, doi:10.3762/bjoc.14.107
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