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1.
Noureddine Raouafi Khaled Boujlel Mohamed Lamine Benkhoud 《Phosphorus, sulfur, and silicon and the related elements》2013,188(12):2471-2482
N-(-1H-Benzimidazol-2-yl) imidates 1a–c react with chlorophosphoramide to give the N-[-1-N,N,N′,N′-tetramethylphosphoramidoyl-1H-benzimidazol-2-yl]-imidates 2a–c or with dichlorophosphoramide to yield the bis[(N-1-benzimidazol-2-yl)-imidate] phosphoramide derivatives 3a–b. The reaction of compounds 2a–c toward primary amines is studied. The obtained amidine derivatives 4a–b were unambiguously characterized by different spectroscopic techniques (IR, 1H, 13C, and 31P NMR, and in some cases MS). 相似文献
2.
Raoudha Abderrahim Khaled Boujlel 《Phosphorus, sulfur, and silicon and the related elements》2013,188(5):995-999
The imidates derived from 3-aminotriazole 1 react with isocyanates and isothiocyanates to give corresponding 1,2,4-triazolo-1,3,5-triazin-4-ones and 1,2,4-triazolo-1,3,5-triazin-4-thiones in a 60–75% overall yield. If the condensation is realized at r.t., then the intermediate 2 can be isolated. 相似文献
3.
Noureddine Raouafi Khaled Boujlel Mohamed Lamine BenKhoud 《Phosphorus, sulfur, and silicon and the related elements》2013,188(7):1387-1395
The condensation of N1-benzimidazolyl amidines 1 with tris(dimethy- lamino)phosphine leads to the corresponding [1,2a]Benzimidazolo-1,3,5,2-triazaphosphorines 3 . The N2-phosphoroamidine intermediates 2′ are isolated and yielded the corresponding cyclic compounds 4 upon heating. The oxidation by sulfur of the compounds 3 gives the thiooxide derivatives 4 . The structure of these compounds is unambiguously confirmed by IR, 1H, 31P, and 13C NMR spectroscopy and by MS for some products. 相似文献
4.
Nada Abdullah Yahya Tamimi Sergey Dobretsov Najwa Al Balushi Jalila Alshekaili Hamed Al Balushi Mahmood Al Kindi Syed Imran Hassan Shadia Al Bahlani Benjamin K. Tsang Ikram A. Burney 《Molecules (Basel, Switzerland)》2021,26(12)
High-grade epithelial ovarian cancer is a fatal disease in women frequently associated with drug resistance and poor outcomes. We previously demonstrated that a marine-derived compound MalforminA1 (MA1) was cytotoxic for the breast cancer cell line MCF-7. In this study, we aimed to examine the effect of MA1 on human ovarian cancer cells. The potential cytotoxicity of MA1was tested on cisplatin-sensitive (A2780S) and cisplatin-resistant (A2780CP) ovarian cancer cell lines using AlamarBlue assay, Hoechst dye, flow cytometry, Western blot, and RT-qPCR. MA1 had higher cytotoxic activity on A2780S (IC50 = 0.23 µM) and A2780CP (IC50 = 0.34 µM) cell lines when compared to cisplatin (IC50 = 31.4 µM and 76.9 µM, respectively). Flow cytometry analysis confirmed the cytotoxic effect of MA1. The synergistic effect of the two drugs was obvious, since only 13% of A2780S and 7% of A2780CP cells remained alive after 24 h of treatment with both MA1 and cisplatin. Moreover, we examined the expression of bcl2, p53, caspase3/9 genes at RNA and protein levels using RT-qPCR and Western blot, respectively, to figure out the cell death mechanism induced by MA1. A significant down-regulation in bcl2 and p53 genes was observed in treated cells compared to non-treated cells (p < 0.05), suggesting that MA1 may not follow the canonical pathway to induce apoptosis in ovarian cancer cell lines. MalforminA1 showed promising anticancer activity by inducing cytotoxicity in cisplatin-sensitive and cisplatin-resistant cancer cell lines. Interestingly, a synergistic effect was observed when MA1 was combined with cisplatin, leading to it overcoming its resistance to cisplatin. 相似文献
5.
Stefani Gamboa-Ramirez Dr. Bruno Faure Dr. Marius Réglier Dr. A. Jalila Simaan Dr. Maylis Orio 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(66):e202202206
The stereoselective copper-mediated hydroxylation of intramolecular C−H bonds from tridentate ligands is reinvestigated using DFT calculations. The computational study aims at deciphering the mechanism of C−H hydroxylation obtained after reaction of Cu(I) precursors with dioxygen, using ligands bearing either activated ( L1 ) or non-activated ( L2 ) C−H bonds. Configurational analysis allows rationalization of the experimentally observed regio- and stereoselectivity. The computed mechanism involves the formation of a side-on peroxide species ( P ) in equilibrium with the key intermediate bis-(μ-oxo) isomer ( O ) responsible for the C−H activation step. The P/O equilibrium yields the same activation barrier for the two complexes. However, the main difference between the two model complexes is observed during the C−H activation step, where the complex bearing the non-activated C−H bonds yields a higher energy barrier, accounting for the experimental lack of reactivity of this complex under those conditions. 相似文献
6.
N. Raouafi M. Freytag P. G. Jones K. Boujlel M. L. BenKhoud 《Structural chemistry》2005,16(2):169-172
The preparation of N-[1-(N,N,N,N-tetramethylphosphoramidoyl)-1H-benzimidazol-2-yl]-proponimidic ethyl ester 2 has been achieved by the reaction of N-(1H-benzimidazol-2-yl)-proponimidic acid ethyl ester 1 with N,N,N,N-tetramethylchlorophosphoramide. The structure of compound 2 has been determined by X-ray diffraction. The results of (1H, 13C, 31P) NMR, IR, EI-MS spectral data are consistent with those obtained from the X-ray diffraction. The compound crystallizes in the triclinic system, following the EsZ conformation. In the crystal, there are two weak C3–H3s1 and C15–H15sO1 intermolecular hydrogen bonds. 相似文献
7.
A simple method for the synthesis of 6-thioxo-[1,3,5]-triazinane-2,4-dione derivatives was reported. The electrogenerated cyanomethyl base obtained from electroreduction of neat acetonitrile assisted the reaction between thiourea derivatives and alkyl or aryl isocyanate. This protocol had the advantage of giving good yields using mild conditions. The obtained products have been identified by spectroscopic data, mass spectrometry, and high-resolution mass spectra or elemental analysis. 相似文献
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9.
Meriem Toumi Noureddine Raouafi Khaled Boujlel Issa Tapsoba Jean-Paul Picard Michel Bordeau 《Phosphorus, sulfur, and silicon and the related elements》2013,188(10):2477-2490
Electrogenerated cyanomethyl anion promotes the reaction between primary or secondary amines, carbon disulfide, and alkyl or benzyl halide. Secondary amines are converted to alkyl or benzyl dithiocarbamates, whereas primary amines give N-substituted alkyl or benzyl 3-amino-2-cyanodithiocrotonates. The mechanisms are discussed. 相似文献
10.
In this Note, we propose and we prove the convergence of a Neumann–Dirichlet algorithm in order to approximate a Signorini problem between two elastic bodies. The idea is to retain the natural interface between the two bodies as numerical interface for the domain decomposition and to replace the Dirichlet problem in [4] by a variational inequality. To cite this article: G. Bayada et al., C. R. Acad. Sci. Paris, Ser. I 335 (2002) 381–386. 相似文献