Results 31 to 40 of about 2,171 (198)

Hydantoins: Synthesis, properties and anticonvulsant activity [PDF]

open access: yesHemijska Industrija, 2009
Hydantoin is a five-membered cyclic ureide that is present in numerous biologically active compounds including antiarrhytmics, anticonvulsants and antitumor agents. This paper describes different ways of synthesis of hydantoin-derivatives, their physical
Trišović Nemanja P.   +2 more
doaj   +1 more source

Pulsed Fe Electro-Oxidation for Catalytic Synthesis of Hydantoin Derivatives

open access: yesInternational Journal of Electrochemical Science, 2016
This paper presents an original and practical organic electrochemical/chemical (EC/C) synthesis to prepare hydantoin derivatives from N-Alkyl-piperidin-4-ones.
S. Santiago-Ruiz   +3 more
doaj   +1 more source

The Pyroglutamate Hydantoin Rearrangement [PDF]

open access: yesEuropean Journal of Organic Chemistry, 2006
Abstract When a mixture of a pyroglutamate and an isocyanate in THF is treated with NaH, a ring transformation occurs leading to functionalised hydantoins. The novel reaction involves a ring‐closing ring‐opening sequence providing a new and straightforward access to an interesting class of heterocyclic compounds. Furthermore, starting
Nicolai Dieltiens   +6 more
openaire   +1 more source

Synthesis, structure and biological properties of active spirohydantoin derivatives [PDF]

open access: yesHemijska Industrija, 2016
Spirohidantoins represent an pharmacologically important class of heterocycles since many derivatives have been recognized that display interesting activities against a wide range of biological targets.
Lazić Anita M.   +4 more
doaj   +1 more source

Cu-catalyzed N-3-Arylation of Hydantoins Using Diaryliodonium Salts

open access: yes, 2020
A general Cu-catalyzed, regioselective method for the N-3-arylation of hydantoins is described. The protocol utilizes aryl(trimethoxyphenyl)iodonium tosylate as the arylating agent in the presence of triethylamine and a catalytic amount of a simple Cu ...
Sandtorv, Alexander Harald   +3 more
core   +1 more source

Biologically Oriented Hybrids of Indole and Hydantoin Derivatives

open access: yesMolecules, 2023
Indoles and hydantoins are important heterocycles scaffolds which present in numerous bioactive compounds which possess various biological activities. Moreover, they are essential building blocks in organic synthesis, particularly for the preparation of ...
Konstantin A. Kochetkov   +2 more
doaj   +1 more source

Lipophilicity assessment of some 5,5-disubstituted hydantoins by the means of reversed phase liquid chromatography [PDF]

open access: yesChemical Industry and Chemical Engineering Quarterly, 2013
The retention of some 5,5-disubstituted hydantoins was investigated by reversed phase high performance thin-layer chromatography (RP HPTLC) and reversed phase high-pressure liquid chromatography (RP HPLC).
Despotović Vesna   +4 more
doaj   +1 more source

New insights in the removal of the hydantoins, oxidation product of pyrimidines, via the base excision and nucleotide incision repair pathways. [PDF]

open access: yesPLoS ONE, 2011
BACKGROUND: Oxidative damage to DNA, if not repaired, can be both miscoding and blocking. These genetic alterations can lead to mutations and/or cell death, which in turn cause cancer and aging.
Modesto Redrejo-Rodríguez   +6 more
doaj   +1 more source

Synthesis and investigation of solvent effects on the ultraviolet absorption spectra of 1, 3-bis-substituted-5, 5-dimethylhydantoins [PDF]

open access: yesJournal of the Serbian Chemical Society, 2003
A series of 1,3-bis-substituted-5,5-dimethylhydantoins was synthesized using the reaction of 5,5-dimethylhydantoin with the corresponding alkyl halide in the presence of trimethylamine as catalyst and sodium hydroxide, according to a modified literature ...
Ušćumlić Gordana S.   +2 more
doaj   +3 more sources

Revisiting the Urech Synthesis of Hydantoins: Direct Access to Enantiopure 1,5-Substituted Hydantoins Using Cyanobenziodoxolone

open access: yes, 2019
A method for the synthesis of enantiopure 1,5-substituted hydantoins was developed using a hypervalent iodine cyanation reagent (cyanobenziodoxolone, CBX) as a source of electrophilic carbon.
Franck Le Vaillant (3211635)   +2 more
core   +1 more source

Home - About - Disclaimer - Privacy