Results 141 to 150 of about 1,728 (205)

3-Aryl-2<i>H</i>-azirines as annulation reagents in the Ni(II)-catalyzed synthesis of 1<i>H</i>-benzo[4,5]thieno[3,2-<i>b</i>]pyrroles. [PDF]

Beilstein J Org Chem
Pavlenko JI, Sakharov PA, Agafonova AV, Isadzhanyan DA, Khlebnikov AF, Novikov MS.   +5 more
europepmc   +1 more source

Cooperative Copper/Lipase Catalysis for the Chemoenzymatic Dynamic Kinetic Resolution (DKR) of Bis(hetero)arenols. [PDF]

JACS Au
Wang K, Peng Y, Lou D, Zhu C.
europepmc   +1 more source

Stereoselective Synthesis of Axially Chiral Allenes and Styrenes via Chiral Phosphoric Acid Catalysis: An Overview. [PDF]

ACS Omega
Woldegiorgis AG, Mustafai A, Muhammad FY, Farooqi R, Tolesa LD, Aimun K.   +5 more
europepmc   +1 more source

Iron(III) Complexes with Luminescence Lifetimes of up to 100 ns to Enhance Upconversion and Photocatalysis. [PDF]

J Am Chem Soc
Wellauer J, Pfund B, Becker I, Meyer F, Prescimone A, Wenger OS.   +5 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

IPC behaviour of some sulphonated naphthols and nitroso-naphthols

Fresenius' Zeitschrift für analytische Chemie, 1988
The 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
openaire   +1 more source

4-Chloro-1-naphthol

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, Bernard, Marciniak   +1 more
openaire   +2 more sources

Metabolism of 1-naphthol by tyrosinase

Biochemical Pharmacology, 1985
1-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, G M, Cohen, T W, Gant, S, Naish, P A, Riley   +4 more
openaire   +2 more sources

Synthesis of Polysubstituted‐2‐naphthols.

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
Hélène Juteau, Yves Gareau, Hugo Lachance   +2 more
openaire   +1 more source

Contact dermatitis from Naphthol AS

Contact Dermatitis, 1990
Naphthol AS, a coupling agent in cotton dyeing, caused allergic contact dermatitis in 5 patients, sensitized from wearing a special kind of shirt. Patch tests with Naphthol AS and pieces of shirt were positive in all 5 patients. Analysis of 1 of the shirts revealed the presence of Naphthol AS.
J, Roed-Petersen, W, Batsberg, E, Larsen
openaire   +2 more sources