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排序方式: 共有123条查询结果,搜索用时 15 毫秒
1.
Dinabandhu Naskar Amrita RoyWilliam L. Seibel David E. Portlock 《Tetrahedron letters》2003,44(31):5819-5821
Tertiary aromatic amines can serve as amine substrates for the Petasis boronic acid-Mannich reaction, providing a practical synthetic route for the CC bond formation of α-(4-N,N-dialkylamino-2-alkyloxyphenyl)carboxylic acids. The scope and limitations of this method have been examined. 相似文献
2.
Rupankar PairaArindam Maity Shyamal MondalSubhendu Naskar Krishnendu B. SahuPritam Saha Abhijit HazraE. Padmanaban Sukdeb BanerjeeNirup B. Mondal 《Tetrahedron letters》2011,52(14):1653-1657
Basic alumina supported solvent-free one-pot synthesis of pyridine-fused polycyclic diazepaniums was achieved under microwave irradiation. The process was successfully extended to the synthesis of pyridine-fused bicyclic imidazolidiniums and tetrahydro-pyrimidiniums and also of tri- and tetracyclic diaza-heterocycle-fused quinoliniums. The dual characteristic of basic alumina, a solid support as well as a base, was successfully employed in the current investigation. The method emerged to be an effective route in terms of product yield, reaction time, and ease of purification and most importantly for environment friendly protocols. 相似文献
3.
Subhendu Naskar Priyankar Paira Rupankar Paira Shyamal Mondal Arindam Maity Abhijit Hazra Krishnendu B. Sahu Pritam Saha Sukdeb Banerjee Peter Luger Manuela Webe Nirup B. Mondal 《Tetrahedron》2010,66(27-28):5196-5203
An environmentally benign protocol has been described for the synthesis of novel 2-(1′,3′-dihydro-1H-[2,3′]biindolyl-2′-ylidene)-indan-1,3-diones/bis-indolylindane-1,3-diones from ninhydrin and 3-substituted/unsubstituted indoles. It uses montmorillonite K-10 as catalyst in a solvent-free condition under microwave irradiation. The method was also used for the synthesis of novel bisindolylindeno[1,2-b]quinoxaline derivatives. 相似文献
4.
Kinsuk Das Tarak Nath Mandal Somnath Roy Samik Gupta Anil Kumar Barik Partha Mitra Arnold L. Rheingold Susanta Kumar Kar 《Polyhedron》2010
The varying coordination modes of the title ligand, L [5-methyl-1-(pyridin-2-yl)-N′-[pyridin-2-ylmethylidene]pyrazole-3-carbohydrazide] towards the different metal centers is reported by preparation and characterization of Cu(II), Zn(II) and Cd(II) complexes, [Cu(L)NO3.H2O](NO3) (1) [Zn(L)2](ClO4)2·2DMF (2) and [Cd(L)(I)2] (3) respectively. In 1, the neutral ligand serves as tetradentate 4 N donor where both pyridine and pyrazole nitrogen atoms of pyridyl–pyrazole part are coordinatively active, leaving the carbonyl oxygen of the carbohydrazide part inactive. The same pyridine and pyrazole N atoms remain abstained from the coordination process towards the Zn(II) and Cd(II) metal centers. For 2 and 3 the ligand behaves as a tridentate NNO donor where the two nitrogen atoms come from azomethine, pyridine of pyridine-2-carbaldehyde parts and O from carbonyl oxygen atoms (carbohydrazide part). The complex 1 and 2 are distorted octahedral while complex 3 adopts distorted square pyramidal geometry. All the complexes are X-ray crystallographically characterized. 相似文献
5.
Jnan Prakash Naskar Chiranjan Biswas Liping Lu Miaoli Zhu 《Journal of chemical crystallography》2011,41(4):502-507
Abstract
Schiff-base condensation of a equimolar proportion of diacetyl-monoxime monohydrazone and 1-methylimidazole-2-carboxaldehyde in methanol gives rise to the imidazole azine, 3-(1-methylimidazol-2-yl)methylenehydrazonobutan-2-one oxime(HL). Reaction of 1:1 stoichiometric proportion of HL with copper(II)perchlorate hexahydrate in methanol yields a dimeric oximato bridged copper compound, [Cu2L2(H2O)2](ClO4)2 (1). The compound is characterized by C, H and N analyses, FT-IR, ESI–MS, conductivity measurement, UV–Vis spectra and X-ray single crystal diffraction. The title compound (1) crystallizes in the monoclinic space group P21/c with a = 6.8533 (8), b = 18.413 (2), c = 11.7399 (14) ?, β = 93.685 (2)°, V = 1478.4 (3) ?3 and Z = 2. The geometry around each copper center is distorted square pyramidal. The copper(II) dimer shows antiferromagnetic interaction mediated by symmetric disposition of oximato groups. 相似文献6.
Subhendu Naskar 《Tetrahedron letters》2010,51(10):1437-1531
A high yielding green protocol has been developed for the synthesis of tri-, tetra-, and pentacyclic fused 2-quinolones in micellar medium. The method is more effective compared to phase-transfer catalytic (PTC) method in terms of the yield of the product as well as the reaction time. It is operationally simple as well as environmentally benign. 相似文献
7.
Exploring the effect of radiation crosslinking on the physico‐mechanical,dynamic mechanical and dielectric properties of EOC–PDMS blends for cable insulation applications
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This work focuses on the effect of electron beam irradiation on the physico‐mechanical, dynamic mechanical and dielectric properties of blends based on ethylene octene copolymer (EOC) and poly dimethyl siloxane (PDMS) rubber. It is found that electron beam irradiation caused considerable improvement in the physico‐mechanical properties; the tensile strength was enhanced by nearly 35% for 70:30 EOC:PDMS blend. Phase morphology of the blends analyzed before irradiation by scanning electron microscopy (SEM) exhibited droplet/matrix morphology with sizes of the PDMS rubber domain varying from 0.55 µm to 0.47 µm as the amount of PDMS rubber decreased from 30 wt% to 10 wt%. This reduction in the PDMS rubber domain has been correlated with the physico‐mechanical properties of the blends. Further, the dynamic mechanical properties and creep behavior of these EOC:PDMS blends before and after irradiation has been studied. It is inferred that the 70:30 blend after radiation crosslinking shows a 17% decrease in the creep compliance, i.e. higher creep resistance compared to neat blends. All the radiation crosslinked blends exhibited lower dielectric constant, lower dielectric loss and higher electrical resistivity as compared to the virgin blends which makes it suitable for cable insulating application. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
8.
Shuvankar Naskar Rweetuparna Guha Jens Müller 《Angewandte Chemie (International ed. in English)》2020,59(4):1397-1406
The incorporation of metal ions into nucleic acids by means of metal‐mediated base pairs represents a promising and prominent strategy for the site‐specific decoration of these self‐assembling supramolecules with metal‐based functionality. Over the past 20 years, numerous nucleoside surrogates have been introduced in this respect, broadening the metal scope by providing perfectly tailored metal‐binding sites. More recently, artificial nucleosides derived from natural purine or pyrimidine bases have moved into the focus of AgI‐mediated base pairing, due to their expected compatibility with regular Watson–Crick base pairs. This minireview summarizes these advances in metal‐mediated base pairing but also includes further recent progress in the field. Moreover, it addresses other aspects of metal‐modified nucleic acids, highlighting an expansion of the concept to metal‐mediated base triples (in triple helices and three‐way junctions) and metal‐mediated base tetrads (in quadruplexes). For all types of metal‐modified nucleic acids, proposed or accomplished applications are briefly mentioned, too. 相似文献
9.
Dipankar Mishra Subhendu Naskar Shyamal K. Chattopadhyay Milan Maji Parbati Sengupta Rupam Dinda Saktiprasad Ghosh Thomas C. W. Mak 《Transition Metal Chemistry》2005,30(3):352-356
The synthesis, crystal structure, redox and spectroscopic properties of trans-[Ru(bbpH2)(PPh3)2Cl]Cl are reported. In the crystalline solvate trans-[Ru(bbpH2)(PPh3)2cCl]Cl CHCl3 H2O, the molecular components are connected by strong intermolecular hydrogen bonding to form an infinite double column. 相似文献
10.
Two important configurations of Yang-Mills fields are discussed applying to them the Painleve test of Ablowitz. The case with a constant electric E-field does not admit an exact solution while the cylindrically symmetric self-dual system admits an inverse scattering approach for instanton solution. 相似文献