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Cet article examine les divers modes d'oxygénation des phénols, naphtols, anthranols et flavonols en mettant en évidence, dans la mesure du possible, la formation des peroxydes intermédiaires.Ainsi, en plus des éléments fournis dans d'autres publications
Karnojitzky V. J.
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Pd‐Catalyzed Asymmetric Dearomative Heck/Tsuji‐Trost Difunctionalization of Naphthalenes
We have developed a palladium‐catalyzed asymmetric dearomative Heck/Tsuji‐Trost 1,4‐difunctionalization reaction of naphthalenes, affording 4‐aminospirocyclohexene oxindole products bearing two remote chiral centers. Through the effect of the newly designed chiral sulfinamide phosphine ligand with large steric hindrance, side reactions are inhibited ...
Long‐Ling Ma +3 more
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An efficient one-pot synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthols is described. This involves the three-component reaction of β-naphthol, aromatic aldehydes and 2-aminobenzothiazole in the presence of a catalytic amount of ...
Limin Yang
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Amidoalkyl naphthols are synthesized via a simple, one-pot, three-component reaction between aldehydes, 2-naphthol and amides or ureas using polyphosphate ester (PPE) as a reaction mediator under solvent-free conditions in good to excellent yields.
Hassan Moghanian, Sattar Ebrahimi
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The two naphthol isomers were investigated in different organic solvents by taking cyclic voltammograms, and fouling took place on a platinum electrode surface, except for dimethyl sulfoxide and dimethyl formamide. Studies in allyl alcohol rarely used in
László Kiss +2 more
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Synthesis and application of novel heterocyclic dyes based on 11-amino-13H-acenaphtho[1,2-e]pyridazino[3,2-b]-quinazoline-13-one [PDF]
A new fused heterocyclic compound, 11-amino-13H-acenaphtho[1,2-e]pyridazino [3,2-b]quinazolin-13-one was synthesized and used to prepare a novel series of heterocyclic mono azo dyes by coupling with various naphthols.
Patel Vijay J. +2 more
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Arylglycine-derivative synthesis via oxidative sp3 C–H functionalization of α-amino esters
An efficient method for the synthesis of arylglycine derivatives is described. The oxidative coupling reactions of naphthols and phenols with α-amino esters proceeded smoothly in the presence of meta-chloroperoxybenzoic acid as an oxidant under ambient ...
Zhanwei Xu +3 more
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Ninhydrin and related indanone scaffolds are employed as effective synthon in organic and bioorganic chemistry. In the present work, the reactivity of ninhydrin is exploited to synthesize various cyclic and acyclic compounds using mortar and pestle ...
Suven Das +4 more
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A rapid and efficient one-pot method for the synthesis of 1-amidoalkyl-2-naphthols has been developed in the presence of mixed-addenda vanadium(V)-substituted polyoxomolybdates including: H3+xPMo12-xVxO40 (x=1-3) heteropolyacids (HPAs) as recyclable ...
Fatemeh F. Bamoharram +3 more
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A potassium carbonate promoted tandem oxy-Michael addition/cyclization of α,β-unsaturated carbonyl compounds with naphthol derivatives for the synthesis of 2-substituted naphthopyrans was developed.
Shan-Shan Li +5 more
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