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Catalytic asymmetric intermolecular [4 + 2] annulation of benzocyclobutenones with Alkynes and activated carbonyls via C-C activation. [PDF]
Liu H +8 more
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Recent advances in the transformation reactions of the Betti base derivatives. [PDF]
Olyaei A, Sadeghpour M.
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Stereocontrol in Conformationally Stable C(sp<sup>2</sup>)─C(sp<sup>3</sup>) Atropisomers. [PDF]
Domain A +10 more
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Distribution of Environmental Phenols into Follicular Fluid and Urine of Women Attending Infertility Clinic. [PDF]
Klimowska A +5 more
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Copper-catalysed dynamic kinetic asymmetric C-O cross-coupling to access chiral aryl oxime ethers and diaryl ethers. [PDF]
Zhang MR +8 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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Acta Crystallographica Section C Crystal Structure Communications, 2009
Molecules of the title compound, C(10)H(7)ClO, (I), are connected by a single strong O-H...O hydrogen bond into a simple C(2) chain, which runs parallel to the c axis and is additionally stabilized by intermolecular pi-pi stacking interactions. The significance of this study lies in the comparison drawn between the crystal structure of (I) and those of
Ewa, Rozycka-Sokolowska +1 more
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Molecules of the title compound, C(10)H(7)ClO, (I), are connected by a single strong O-H...O hydrogen bond into a simple C(2) chain, which runs parallel to the c axis and is additionally stabilized by intermolecular pi-pi stacking interactions. The significance of this study lies in the comparison drawn between the crystal structure of (I) and those of
Ewa, Rozycka-Sokolowska +1 more
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Metabolism of 1-naphthol by tyrosinase
Biochemical Pharmacology, 19851-Naphthol was metabolized by the polyphenol oxidase, tyrosinase, primarily to 1,2-naphthoquinone and to small amounts of 1,4-naphthoquinone as well as to covalently bound products. The inhibition of covalent binding by ethylenediamine, which reacts specifically with 1,2-naphthoquinone but not 1,4-naphthoquinone, suggested that most of the covalent ...
D, Doherty M +4 more
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Synthesis of Polysubstituted‐2‐naphthols.
ChemInform, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
Hélène Juteau +2 more
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