Csp2-H functionalization of phenols: an effective access route to valuable materials via Csp2-C bond formation. [PDF]
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Visible-light-enabled excited-state dearomatization reactions. [PDF]
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Atroposelective Construction of Biaryls Enabled by a Ni(II)-Catalyzed Aerobic Oxidation Strategy. [PDF]
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Catalyst-controlled regiodivergence in enantioselective synthesis of spirocyclic γ- versus δ-lactams. [PDF]
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Methyl itaconate-anthracene adducts (MIAs) facilitate the enantiomeric separation of 1,1'-bi-2-naphthols <i>via</i> thin-layer chromatography (TLC) with trends predicted by molecular dynamics simulations. [PDF]
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Efficient construction of a β-naphthol library under continuous flow conditions. [PDF]
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Investigating the Binding Mode of a Naphthol-Based Inhibitor Targeting SARS-CoV-2 Main Protease. [PDF]
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IPC behaviour of some sulphonated naphthols and nitroso-naphthols
Fresenius' Zeitschrift für analytische Chemie, 1988The ion-pair chromatographic behaviour of a naphthol and some sulpho-substituted naphthols and nitroso-naphthols is studied. Formation of the ion-pair compounds is done either by pre-extraction or during elution with long-chained quaternary alkyl- or alkylarylammonium salts.
H. Sirén, R. Dammert, L. Huhanantti
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