Results 51 to 60 of about 3,621 (239)
Hydrogen-Transfer-Mediated N‑Arylation of Naphthols Using Indolines as Hydrogen Donors
Using a hydrogen-transfer-mediated activation mode, we report a new catalytic system for the transfer hydrogenation of naphthols. In the presence of the Pd/C catalyst and base, various naphthols reacted with indolines to afford N-aryl-substituted ...
Yibiao Li (2078623) +13 more
core +1 more source
Development of ProPhenol/Ti(IV) Catalyst for Asymmetric Hydroxylative Dearomatization of Naphthols
By development of ProPhenol/Ti(IV) catalysts, a catalytic enantioselective hydroxylative dearomatization of naphthols is achieved by using TBHP as a simple oxidative reagent. The side coordinative chain equipped on the C1-position of β-naphthols plays an
Linqing Wang (1470319) +15 more
core +1 more source
In this work, a novel biomolecule/semiconductor hybrid catalyst was prepared by loading anthraquinone‐liked juglone onto anatase TiO2. This catalyst exhibited high photocatalytic activity for H2O2 production. Hydrogen peroxide (H2O2) is a vital oxidant with broad industrial applications, and its production via photocatalysis represents a highly ...
Zengyin He +4 more
wiley +1 more source
Two efficient and direct procedures have been developed for the preparation of 1-amidoalkyl-2-naphthols by a one-pot condensation of aldehydes, 2-naphthol, and amides in the presence of trichloroacetic acid or cobalt (II) chloride as catalyst.
Zahed Karimi-Jaberi +2 more
doaj +1 more source
A three-component reaction of naphthols, sulfur dioxide, and aryldiazonium tetrafluoroborates catalyzed by iron(iii) chloride through a radical process via direct C–H functionalization is developed, leading to diverse sulfonated naphthols in good yields.
Mo Chen +3 more
core +1 more source
Nucleophilic Reactions of Cyclobutenones and the Related 4,4‐Dichlorocyclobutenone Derivatives
Cyclobutenone derivates and their 4,4‐dichloro counterparts have an uninterrupted attention as useful synthons in the synthesis of complex organic molecules. Their nucleophilic reactions remain underexplored. This review brings attention to these reactions, whose outcome is not straightforward.
Sarah J. Wright +2 more
wiley +1 more source
Imidazolium salts are shown to catalyze the rapid room temperature reaction of indoles or naphthol with aldehydes to provide bis(indolyl)methanes or bis(naphthol)methane in excellent yields and the reaction proceeds optimally in dichloromethane with no ...
Xu Wang, Courtney C Aldrich
doaj +1 more source
The chemoselective reaction of the C- followed by the O-centered naphthyl radicals with the more electron-deficient hypervalent bond of the diaryliodonium(III) salts is described.
Yuvraj Satkar +5 more
doaj +1 more source
Radical scavenging effects of 1-naphthol, 2-naphthol, and their sulfate-conjugates
1-Naphthol (1-Nap) and 2-naphthol (2-Nap) are phenolic isomers that may be subjected to sulfate conjugation in vivo. Phase-II sulfate conjugation of phenolic compounds is generally thought to result in their inactivation. This study aimed to investigate the antioxidative effects of 1-NapS and 2-NapS, in comparison with their unsulfated counterparts ...
Sugahara, Shintaro +10 more
openaire +3 more sources
Organocatalyzed Intermolecular Asymmetric Allylic Dearomatization of Both α- and β‑Naphthols
The first highly stereoselective intermolecular catalytic asymmetric dearomatization (CADA) of α-naphthols through C–C formation and the first asymmetric allylic dearomatization of naphthols by chiral organocatalysis have been achieved.
Binmiao Yang (6155915) +5 more
core +1 more source

