نتایج جستجو برای: 34 dihydropyrimidin 2 1h thione

تعداد نتایج: 2609081  

Sedigheh Jahanbakhshi Soheil Sayyahi, Zahra Dehghani

In this study, a variety of 3, 4-dihydropyrimidin-2(1H)-ones derivatives were synthesized via three-component Biginelli reaction. The quaternary ammonium- treated clay -catalyzed process proved to be simple, efficient, and environmentally friendly.

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2005
ahmad shaabani ayoob bazgir sakineh arab ameri masoumeh sharifi kiasaraie sima samadi

alkali and alkaline earth metals hydrogen sulfate catalyzed the one-pot three component condensation reactions of aldehydes, 1,3-dicarbonyl compounds and urea or thiourea under solvent-free conditions leading to 3,4-dihydropyrimidin-2(1h)-ones in high yields at 80 °c. our results showed that biginelli reaction not only is ph dependent, but the cation of catalyst plays an important role.

Journal: :international journal of heterocyclic chemistry 0
ali ezabadi central tehran branch, islamic azad university, sanat square, tehran, iran neda ghassemi central tehran branch, islamic azad university, sanat square, tehran, iran

d-tartaric acid is successfully used as a green and efficient catalyst for the synthesis of 3,4-dihydropyrimidin-2(1h)-ones under solvent-free conditions. the developed method has many advantages, including devoid of harmful catalyst and solvents, high yield and easily work-up.

Mehdi Behvandi Behvandi Soheil Sayyahi,

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.

In this work, the ionic liquid triethylamine-bonded sulfonic acid {[Et3N–SO3H]Cl}, N,N-diethyl-N-sulfoethanammonium chloride was used as a green acidic homogeneous catalyst to synthesis of 3,4-dihydropyrimidin-2(1H)-ones and 3,4-dihydropyrimidin-2(1H)-thiones as two categories of heterocycles, from aldehyde, dicarbonyl compound and urea or thiourea throughout the one-pot three components cycloc...

Alireza Kiasat Mohammad Kazem Mohammadi, Parya Nasehi

3,4-dihydropyrimidin-2(1H)-thiones were synthesized in the presence of Ag nanoparticle/melamine sulfonic acid (MSA) supported on silica gel. The reaction was carried out at 110 oC for 20 min under solvent free conditions. In all cases, the three component reaction proceeded smoothly to give the corresponding 3,4-dihydropyrimidin-2(1H)-thiones in moderate to good yield. We have found the best co...

2011
Xi-Zai Zhao Jing-Jing Jia Miao Ou-Yang Fu-Ping Huang Yi-Min Jiang

The title multifunctional twisted organic ligand, C(10)H(10)N(4)S(2), contains a short C=S bond [1.671 (2) Å]. The dihedral angle between the two pyrazine rings is 39.83 (6)°. In the crystal, inter-molecular C-H⋯N and C-H⋯S hydrogen bonds result in the formation of a supra-molecular network.

Journal: :journal of the iranian chemical research 0
bi bi fatemeh mirjalili department of chemistry, college of science, yazd university, yazd, iran esmat mohammadnejad 1department of chemistry, college of science, yazd university, yazd, iran abdolhamid bamoniri department of organic chemistry, faculty of chemistry, university of kashan, kashan, iran

nano-sbcl5.sio2 and sbcl5.sio2 are bench-top catalysts which are reusable, readily available, versatile andefficient for promotion of many acid catalyzed organic reactions. these catalysts do not need specialprecautions for preparation, handling or storage, and they can be stored at an ambient temperature for monthswithout losing their catalytic activity. 4-dihydropyrimidin-2(1h)-ones(thiones) ...

Journal: :Molecular pharmacology 2012
Ja Hyun Koo Woo Hyung Lee Chan Gyu Lee Sang Geon Kim

Fyn kinase has emerged as a regulator of diverse pathological processes. However, therapeutic Fyn inhibitors are not available. This study investigated the potential of a series of cycloalkane-fused dithiolethiones (CDTs) or other congeners to increase antioxidant capacity in association with Fyn inhibition, as well as the molecular basis for this effect. Treatment of HepG2 cells with each agen...

Journal: :Acta Crystallographica Section E Structure Reports Online 2010

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