جستجوی مقالات مرتبط با کلیدواژه "dihydropyrimidinones" در نشریات گروه "شیمی"

An effective one-pot synthesis of dihydropyrimidinonoes in solvent free conditions using CuCl2 as an inexpensive and readily available reagent through Biginelli condensation reaction of aldehyde derivatives, 1,3-dicarbonyl compounds and urea is described. Excellent yields, short reaction times for formation of the products and simple work-up are attractive features of this green protocol. we now wish to report a facile and rapid one-pot solvent free three component procedure preparation of DHPMs derivatives with CuCl2 as a non-toxic, reusable, inexpensive and easily available reagent, under solvent-free conditions at the range of temperatures. we now wish to report a facile and rapid one-pot solvent free three component procedure preparation of DHPMs derivatives with CuCl2 as a non-toxic, reusable, inexpensive and easily available reagent, under solvent-free conditions at the range of temperatures.

An effective one-pot synthesis of dihydropyrimidinonoes in solvent free conditions using CuCl2 as an inexpensive and readily available reagent through Biginelli condensation reaction of aldehyde derivatives, 1,3-dicarbonyl compounds and urea is described. Excellent yields, short reaction times for formation of the products and simple work-up are attractive features of this green protocol.

An effective one-pot synthesis of dihydropyrimidinonoes in solvent free conditions using CuCl2 as an inexpensive and readily available reagent through Biginelli condensation reaction of aldehyde derivatives, 1,3-dicarbonyl compounds and urea is described. Excellent yields, short reaction times for formation of the products and simple work-up are attractive features of this green protocol.

An effective one-pot synthesis of dihydropyrimidinonoes in solvent free conditions using CuCl2 as an inexpensive and readily available reagent through Biginelli condensation reaction of aldehyde derivatives, 1,3-dicarbonyl compounds and urea is described. Excellent yields, short reaction times for formation of the products and simple work-up are attractive features of this green protocol.

An effective one-pot synthesis of dihydropyrimidinonoes in solvent free conditions using CuCl2 as an inexpensive and readily available reagent through Biginelli condensation reaction of aldehyde derivatives, 1,3-dicarbonyl compounds and urea is described. Excellent yields, short reaction times for formation of the products and simple work-up are attractive features of this green protocol.

In this paper, 4,4ʹ-bipyridinium dichloride  supported SBA-15 (SBA@BiPy2+ 2Cl-) was used for the synthesis of dihydropyrimidinones. The synthesized catalyst was characterized by FT-IR spectroscopy, scanning electron microscopy (SEM), Transmission electron microscopy (TEM) and Thermogravimetric analysis (TGA). This nanocomposite was shown to be an efficient heterogeneous catalyst for the synthesis of dihydropyrimidinones derivatives via one-pot multicomponent method under solvent-free conditions. In addition, the catalyst can be recycled several times with no significant loss of catalytic activity.

Multiwalled carbon nanotubes (MWCNTs) have been functionalized with -SO3H groups using new three steps chemical routes. Firstly, OH groups have been attached to CNT surfaces through a radical reaction. The second step involves converting the hydroxyl groups into the oxide one and last step included the attachment of –SO3H groups on the MWCNTs surfaces in the presence of 1-butyl-3-methyl imidazolium tetrafluoroborate [bmim]BF4 ionic liquid as catalyst. Functionalized MWCNTs were characterized by Fourier transform infrared (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and Raman Spectroscopy. Obtained product have be used as acidic nano catalyst in the Biginelli reaction for the synthesis of 3,4-dihydropyrimidin-2(1H)-one derivatives. The reaction was performed under solvent-free conditions with excellent yields and short reaction times in the presence of a reusable efficient catalyst.

In this study, an efficient and green process for the synthesis of dihydropyrimidin-2(1H)-ones from aromatic benzaldehydes, ethyl acetoacetate and urea using Al-MCM-41 as heterogeneous catalyst and microreactor under solvent-free conditions has been developed. The advantages of this method are easy work-up procedure, regeneration of the catalyst, clean and neutral reaction conditions.

An efficient synthesis route to 1,4-dihydropyrimidine derivatives from reaction of divergent aldehydes with ethylacetoacetate and urea under solvent-free conditions by ZnO nanoparticles as a relative in expansive, eco-friendly, easy available, non-volatile, non-explosion, thermally robust, recyclable and easy to handle catalyst at 90°C with excellent yields is described. Unenhanced reaction times, simple reaction protocol and work-up, have been improved synthesis of these materials in the presence of this heterogeneous catalyst.

An effective one-pot synthesis of dihydropyrimidinonoes in solvent free conditions using CuCl2 as an inexpensive and readily available reagent through Biginelli condensation reaction of aldehyde derivatives, 1,3-dicarbonyl compounds and urea is described. Excellent yields, short reaction times for formation of the products and simple work-up are attractive features of this green protocol.