Ara
Toplam kayıt 116, listelenen: 111-116
Green protocol: Catalyst-free synthesis of 2-substituted benzimidazoles under ultrasound irradiation
(Science Reviews 2000 Ltd, 2018)
The synthesis of 2-substituted benzimidazoles from the reaction of o-phenylenediamine and an imino ester hydrochloride with ultrasound irradiation is reported. The procedure has an eco-friendly and simple workup with good ...
A new green protocol for the synthesis of 2-substituted perimidines from hydrazones under catalyst- and solvent-free conditions
(Bulgarian Academy of Sciences, 2018)
A new green protocol was developed for the synthesis of 2-substituted perimidines. The protocol involves a reaction of ethoxy carbonylhydrazone with 1,8-diaminonaphthalene under solvent- and catalyst-free conditions. Simple ...
Efficient synthesis of 2-[(3,4-dichlorophenyl)methyl]-1h-benzimidazole derivatives, and their α-glucosidase inhibitory and antioxidant activities
(Bentham Science Publishers, 2020)
In this work, some new 2-[(3,4-dichlorophenyl)methyl]-1H-benzimidazole derivatives containing different five-membered heterocycles like 1,3,4-oxadiazole, 1,3,4-triazole, and 1,3,4-thiadiazole moieties were designed and ...
Microwave-assisted synthesis of some benzimidazole derivatives containing imine function
(2015)
Benzimidazol modern ilaç keşfinde önemli bir farmakofordur. Birçok benzimidazole türevi yeni ilaç adayı bileşikler elde etmek amacıyla organik kimyacılar tarafından sentezlenmektedir. Bu çalışmada, imin fonksiyonu içeren ...
Synthesis and anticancer activities of amide-bridged coumarin–quinazolinone hybrid compounds
(Springer, 2024)
Abstract: Some novel 3-aminoquinazolin-4(3H)-one derivatives were synthesized by the reaction of 2-aminobenzhydrazide and corresponding iminoester hydrochlorides and then reacted with coumarin-3-carbonyl chloride to obtain ...
Synthesis of novel quinazolinone-triheterocyclic hybrides as dual inhibition of urease and ache
(Springer, 2024)
New triheteroyclic compounds containing quinazolinone, thiophene, andthiadiazole /thiazolidinone structureswere synthesized and characterized by FT-IR, 1H–NMR, and13C–NMRspectral data. The new compounds’ inhibitory activities ...