Results 171 to 180 of about 3,487 (237)
Direct diazotization of indoles with 2-Methoxyethyl nitrite. [PDF]
Hashidoko A +4 more
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Csp2-H functionalization of phenols: an effective access route to valuable materials via Csp2-C bond formation. [PDF]
Brufani G +3 more
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Efficient construction of a β-naphthol library under continuous flow conditions. [PDF]
Shan C, Li R, Wang X.
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Copper-catalyzed yne-allylic substitutions: concept and recent developments. [PDF]
Yang S, Fang X.
europepmc +1 more source
Chiral Copper Catalysis in Enantioselective Domino Reactions. [PDF]
Pellissier H.
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Advances in the Synthesis of Heterocyclic Compounds and Their Applications. [PDF]
Mangalagiu II, Darabantu M.
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Iridium nitrenoid-catalyzed atroposelective C2 arylation of indoles. [PDF]
Mi F, Zheng W, Cao Y, Qi LW, Lu Y.
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Substituted Naphthols: Preparations, Applications, and Reactions
Substituted naphthols (SNs) are an important class of chemical compounds present in many natural and synthetic products with biological and pharmaceutical activities.
Jorge Andres Mora Vargas +2 more
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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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Fungal degradation of 1-naphthol
Canadian Journal of Microbiology, 1972The biological degradation of 1-naphthol was studied during growth, with replacement cultures and cell extracts of the fungus Fusarium solani. Radioactivity of 1-naphthol-1-14C disappeared partially during growth, but it was completely dissipated by cell-extract activity.
J M, Bollag, S Y, Liu
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