Results 111 to 120 of about 5,810 (254)

Chlorierung von α‐Naphthol [PDF]

open access: yesBerichte der deutschen chemischen Gesellschaft, 1911
n ...
openaire   +1 more source

OBSERVATIONS ON NAPHTHOL STAINING AND THE HISTOCHEMICAL LOCALIZATION OF ENZYMES BY NAPHTHOL-AZO DYE TECHNIQUE [PDF]

open access: yesJournal of Histochemistry & Cytochemistry, 1957
A group of naphthols—1- and 2-naphthol, 6-benzoyl-2-naphthol and 6-bromo-2-naphthol—have been investigated in relation to their tissue affinity. It has been found that naphthol binding is mainly dependent on the solubility of the naphthols and on the type of tissue considered.
openaire   +2 more sources

Phase‐Transfer‐Catalyzed Interrupted Barton–Zard Reaction Between Electron‐Deficient Indoles and Benzophenone‐Derived Isocyanides

open access: yesEuropean Journal of Organic Chemistry, Volume 29, Issue 19, 22 May 2026.
A cascade reaction under phase‐transfer conditions between 3‐nitro indoles and isocyanomethylene dibenzenes affords the construction of pyrrolo[3,4‐b]indole cores. Control experiments provide insight into moderate product yields and clarify why the reaction is not amenable to asymmetric induction. A cascade reaction enabling the construction of pyrrolo[
Ana Mikleušević   +4 more
wiley   +1 more source

Anion–π interactions influence pKa values

open access: yesBeilstein Journal of Organic Chemistry, 2011
Five 8-(4-R-phenyl)-1-naphthol derivatives were prepared by PdCl2-catalysed electrophilic aromatic substitution. The pKa' values for these 1,8-disubstituted arene naphthols have been measured in acetonitrile/water (R = NO2, 8.42; R = Cl, 8.52; R = H, 8 ...
Christopher J. Cadman, Anna K. Croft
doaj   +1 more source

Dynamic Kinetic Resolution of Axially Chiral Heterobiaryl N‐Oxides via Peptide‐Catalyzed Aldol Reaction

open access: yesEuropean Journal of Organic Chemistry, Volume 29, Issue 18, 14 May 2026.
Resin‐supported tripeptide achieved the dynamic kinetic resolution in the catalytic aldol reaction of formylated heterobiaryl N‐oxides with high efficiency and enantioselectivity. The system features a broad substrate scope and a recyclable catalyst.
Jiaqi Tian   +3 more
wiley   +1 more source

Risikoanalyse durch eine wirkungsbezogenen Analytik mit der instrumentellen Hochleistungs-Dünnschichtchromatographie in der Lebensmittelüberwachung [PDF]

open access: yes, 2018
Zusammenfassung.: Als wirkungsbezogene Analytik wird die Kopplung von biochemischen bzw. biologischen Testverfahren an chemisch/physikalische oder chromatographische Verfahren bezeichnet.
Oehme-Peter, M., Weins, C.
core  

Functionalized Diaryliodonium Salts with N‐Reactive Amides: Versatile Reactivity for Constructing Benzo‐Fused Nitrogen Heterocycles

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 9, 5 May 2026.
A practical one‐pot strategy for the synthesis of ortho‐amide‐functionalized TMP‐iodonium(III) salts has been developed. These iodonium salts exhibited distinct reactivities toward N‐, O‐, and S‐nucleophiles, facilitating arylocyclization and producing a variety of benzo‐fused heterocycles under mild conditions.
Naoki Miyamoto   +4 more
wiley   +1 more source

Naphthol and lens.

open access: yesIndian journal of medical sciences, 1992
Alpha and beta naphthols, the metabolites of naphthalene, a cataractogenic agent, was tested for it's effect on sheep lens proteases and their inhibitors. It reduced protease activities, not that of inhibitor activities of lens proteins. It also increased the efflux of free amino acid from lenses which was retarded by a high concentration of tissue ...
openaire   +1 more source

O2‐Mediated Cu‐Catalyzed Dehydrogenative Sulfilimination of Tyrosines and Bioactive Phenols

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 9, 5 May 2026.
We report herein the mild O2‐mediated Cu‐catalyzed dehydrogenative sulfilimination of diverse bioactive phenols with simple sulfenamides. The bioconjugation of unmodified native peptides, in particular at their tyrosine units with the dehydrogenative phenochalcogenazination reaction, has attracted much attention lately due to potential click type ...
Fang Xiao, Frederic W. Patureau
wiley   +1 more source

Catalytic Enantioselective Synthesis of Conformationally Stable C(sp2)−C(sp3) Naphthocoumarin Atropisomers

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 9, 5 May 2026.
The enantioselective synthesis of naphthocoumarin adducts via a tandem organocatalytic 1,4‐addition/decarboxylation delivers excellent control over a newly forged stereocenter and yields configurationally stable synclinal atropisomers. The process features broad substrate scope and scalability, and its structural and mechanistic foundations are ...
M. Chiara Cabua   +10 more
wiley   +1 more source

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