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排序方式: 共有161条查询结果,搜索用时 31 毫秒
1.
The present paper establishes sufficient conditions for the uniformly bounded of any solution of (1.1) and which tend to zero as t → ∞. 相似文献
2.
Novel products from attempted michael addition to 1-methyl-1,2,5,6-tetrahydropyridine-4-carbonitrile
Graeme L. Butt Leslie W. Deady Maureen F. Mackay Maruse Sadek 《Tetrahedron letters》1982,23(43):4485-4488
The reaction of some phenols with the title compound, in the presence of sodium, gives 2-(2-hydroxyaryl_piperidine derivatives. Geometrical isomers have been separated, which differ in having an equatorial (A) or axial (B) cyano group on the piperidine chair (the methyl and aryl groups are equatorial in both forms). The x-ray crystallographic structures of an example of each of A and B are reported and the proton NMR spectra are assigned. 相似文献
3.
Ramadan Ahmed Mekheimer Kamal Usef Sadek Hisham Ahmed Abd El‐Nabi Afaf Abd El‐Hameid Mohamed Ehab Anwer Ebraheem Michael B. Smith 《Journal of heterocyclic chemistry》2005,42(4):567-574
Ethyl 3‐amino‐4‐chlorothieno[3,2‐c]quinoline‐2‐carboxylate ( 4 ) is a versatile synthon, prepared by reacting an equimolar amount of 2,4‐dichloroquinoline‐3‐carbonitrile ( 1 ) with ethyl mercaptoacetate ( 2 ). Ethyl 5‐alkyl‐5H‐1‐thia‐3,5,6‐triazaaceanfhrylene‐2‐carboxylates 9a‐c , novel perianellated tetracyclic heteroaro‐matics, were prepared by refluxing 4 with excess of primary amines 7a‐c to yield the corresponding amino‐thieno[3,2‐c]quinolines 8a‐c . Subsequent reaction with an excess of triethyl orthoformate (TEO) furnished 9a‐c . Reaction of 4 with TEO in Ac2O at reflux, gave the simple acetylated compounds, thieno[3,2‐c]‐quinolines 12 and 13 . Refluxing 4 with benzylamine ( 7d ) gave 10 , and subsequent treatment with TEO gave the tetracyclic compound 11 . Refluxing 13 with an excess of alkylamines 7a‐d gave the fhieno[3,2‐c]quino‐lines 15 . Refluxing the aminothienoquinolines 8b with an excess of triethyl orthoacetate gave thieno[3,2‐c]quinoline 17 , while heating with Ac2O gave 18 and 19 , with small amounts of 16 . Reaction of 8a,b with ethyl chloroformate and phenylisothiocyanate generated the new 1‐thia‐3,5,6‐triazaaceanthrylenes 20a,b and 21a,b , respectively. Diazotization of 8a‐c afforded the novel tetracyclic ethyl 5‐alkyl‐5H‐1‐fhia‐3,4,5,6‐tetraazaaceanthrylene‐2‐carboxylates 22a‐c in good yields. 相似文献
4.
M. B. Alamin A. A. Mhapes A. M. Bejey A. Sadek R. H. Atweer K. Dubali Daw M. Saad 《Journal of Radioanalytical and Nuclear Chemistry》2007,271(1):247-250
Since there is no database in Libya defining the intake of the individuals from different essential (minor and trace) and
toxic elements provided through food, drinking water and aerosol, a project has been proposed with the cooperation of IAEA
to determine the concentration of a number of elements such as Cs, Fe, Cr, Rb, Sc, Se, Co, Zn in the three mentioned sources.
Emphasis was placed on the use of nuclear and nuclear-related techniques. In this paper, the primary results are presented
for the concentration of minor and trace elements in some vegetables, spices and other foods which are widely used in the
Libyan meals. Instrumental neutron activation analysis utilizing a 10 MW water pool reactor and a γ-ray spectroscopy facility
was employed. For quality control, certified reference materials were analyzed simultaneosly with the samples which show good
agreements compared with the certified data. Emphasis was given to both elements iron and zinc for their importance. 相似文献
5.
6.
Nabil Abdul‐kader Saleh Hussein El‐abd Saltani Fadhil Abbas Al‐Issa Al‐Sadek Gomaa Melad 《中国化学会会志》2013,60(10):1234-1240
The antimicrobial activity of thirteen newly synthesized 4‐thiazolidinones (TZONs) and four dithiolane derivatives was assessed against susceptible and resistant bacteria, including MRSA, as well as Candida albicans. The structure‐activity relationships revealed that 4‐Thiazolidinone derivatives harboring p‐chlorophenyl and dicarboxyethyl at the 2‐ethenyl and 5‐arylidine positions of the thiazolidinone ring display considerable antibacterial properties. No antifungal activity was recorded by all tested compounds against Candida albicans. The possible potentiative (synergistic) effect of the most active compounds to a few commercial antibiotics was also investigated. 相似文献
7.
Nabil Abdul‐Kader Saleh Hussein El‐Abd Saltani Fadhil Abbas Al‐Issa Ahmad Abul‐kasem Errabie Al‐Sadek Gomaa Melad 《中国化学会会志》2013,60(11):1353-1358
The antifungal and antioxidant activities of thirty newly synthesized 4‐thiazolidinone (TZON) derivatives were assessed against some fungal species including Candida albicans and Aspergillus niger. The introduction of different arylidene moieties at 5‐positions of the thiazolidinone ring successfully enhanced its biological activity. The structure–activity relationships revealed that 4‐thiazolidinone derivatives harboring dicarboxyethyl (at the 2‐ethenyl) and p‐nitrophenylhydrazyl arm (at the 5‐arylidine positions of the thiazolidinone ring) display considerable antifungal and antioxidant properties. 相似文献
8.
9.
The synthesis of several new polyfunctionally substituted fused pyrazoles via reaction of 5‐amino‐3‐methylthio‐1H‐pyrazole‐4‐carboxylate ( 2 ) with different reagents is described. 相似文献
10.
A new series of 1,3-thiazole and benzo[d]thiazole derivatives 10-15 has been developed, characterized, and evaluated for in vitro antimicrobial activity at concentrations of 25-200 μg/mL against Gram+ve organisms such as methicillin-resistant Staphylococcus aureus (MRSA), Gram-ve organisms such as Escherichia coli (E. coli), and the fungal strain Aspergillus niger (A. niger) by the cup plate method. Ofloxacin and ketoconazole (10 μg/mL) were used as reference standards for antibacterial and antifungal activity, respectively. Compounds 11 and 12 showed notable antibacterial and antifungal activities at higher concentrations (125-200 μg/mL), whereas benzo[d]thiazole derivatives 13 and 14 were found to display significant antibacterial or antifungal activity (50-75 μg/mL) against the Gram+ve, Gram-ve bacteria, or fungal cells used in the present study. In addition, a correlation between calculated and determined partition coefficient (log P) was established which allows future development of compounds within this series to be carried out based on calculated log P values. Moreover, compounds 13 and 14 show that the optimum logarithm of partition coefficient (log P) should be around 4. 相似文献