排序方式: 共有49条查询结果,搜索用时 15 毫秒
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Sanjay Jadhav Gajanan Rashinkar Rajashri Salunkhe Arjun Kumbhar 《Tetrahedron letters》2017,58(33):3201-3204
A simple, efficient and metal-free route for the synthesis of dissymmetric ketones through Suzuki type cross-coupling reaction has been established. This strategy signifies an attractive, cost-effective and operationally convenient tool for the synthesis of a wide range of dissymmetric ketones. Although conventional routes for the synthesis of ketones have been widely used, the potential challenge with these methods is functional group tolerance. The reported metal-free method represents a reaction with moderate functional group tolerance. The procedure is operationally convenient and shows broad substrate scope with good to excellent product yields. 相似文献
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Pawar Arvind Gajare Shivanand Patil Audumbar Kurane Rajanikant Rashinkar Gajanan Patil Suresh 《Research on Chemical Intermediates》2021,47(7):2801-2820
Research on Chemical Intermediates - Magnetic separable nanoparticles-decorated N-heterocyclic carbene complex with copper (MNP[1-Methyl benzimidazole]NHC@Cu) has been prepared by covalent grafting... 相似文献
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Shivanand Gajare Megha Jagadale Altafhusen Naikwade Prakash Bansode Gajanan Rashinkar 《应用有机金属化学》2019,33(6)
Ferrocene tethered N‐heterocyclic carbene‐copper complex anchored on graphene ([GrFemImi]NHC@Cu complex) has been synthesized by covalent grafting of ferrocenyl ionic liquid in the matrix of graphene followed by metallation with copper (I) iodide. The [GrFemImi]NHC@Cu complex has been characterized by fourier transform infrared (FT‐IR), fourier transform Raman (FT‐Raman), CP‐MAS 13C NMR spectroscopy, transmission electron microscopy (TEM), thermogravimetric analysis (TGA), energy dispersive X‐ray (EDX) analysis, X‐ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET) surface area analysis and X‐ray diffractometer (XRD) analysis. This novel complex served as a robust heterogeneous catalyst for the synthesis of bioactive N‐aryl sulfonamides from variety of aryl boronic acids and sulfonyl azides in ethanol by Chan‐Lam coupling. Recyclability experiments were executed successfully for six consecutive runs. 相似文献
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Jagannath Jadhav Sharanabasappa KhanapaureRajanikant Kurane Rajashri SalunkheGajanan Rashinkar 《Tetrahedron letters》2013
An unprecedented methodology for the facile synthesis of 2-substituted 3-cyano-4-azaindoles using modified Madelung synthesis is described. The methodology relies on acid and amine coupling under very mild conditions. 相似文献
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Jagannath Jadhav Sharanabasappa Khanapure Rajashri Salunkhe Gajanan Rashinkar 《应用有机金属化学》2013,27(8):486-488
Zirconocene dichloride (Cp2ZrCl2) in the presence of DMF was found to be a highly efficient catalyst for the synthesis of structurally diverse 2‐substituted quinozolin‐4(3H)‐ones by reaction of anthranilimide with a wide range of aryl aldehydes. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
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R. Santhosh Reddy Tanveer Mahamadali Shaikh Varun Rawat Pratibha U. Karabal Gajanan Dewkar Gurunath Suryavanshi Arumugam Sudalai 《Catalysis Surveys from Asia》2010,14(1):21-32
A novel, exceptionally stable titanium superoxide radical ion was prepared and its structure determined by FTIR, ESR, Raman
spectroscopy, X-ray diffraction, thermogravimetric/differential thermal analysis and elemental analysis. This heterogeneous
catalyst has been found to be effective for the selective oxidation of aromatic amines and phenols to the corresponding nitro
aromatics and p-quinones, respectively. In addition, this non-toxic, inexpensive and reusable catalyst has also been used in aminobromination
of olefins, which proceed to give the 1, 2-bromoaminated anti-Markovnikov product. A brief account of these results is summarized in this review. 相似文献
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Kalaga Mahalakshmi Naidu Rudresh Naik Gajanan Kondapalli Venkata Gowri Chandra Sekhar 《Arabian Journal of Chemistry》2019,12(8):2418-2429
A series of thirty-six novel 5-(2-(4-(benzo[d]isoxazol-3-yl)piperazin-1-yl)acetyl)indolin-2-one and 5-(2-(4-substitutedpiperazin-1-yl)acetyl)indolin-2-one analogues were synthesized, characterized and screened for their in vitro anti-tubercular activity against Mycobacterium tuberculosis H37Rv strain. These compounds exhibited minimum inhibitory concentration between 1.56 and 50 μg/mL. Among these derivatives, compounds 10c, 10d, 10j, 10o and 10v (MIC 6.25 μg/mL) displayed moderate activity, while compounds 10e, 10l, 10q, 10w,10x, 12d, 12e and 12i (MIC 3.12 μg/mL) showed good anti-tubercular activity and compounds 10f, 10k, 10p, 10r, 12f, 12j and 12k (MIC 1.56 μg/mL) exhibited excellent anti-tubercular activity. In addition, MTT assay was accomplished on the active analogues of the series against mouse macrophage (RAW 264.7) cells to evaluate the cytotoxic effect of the newly synthesized compounds and selectivity index of the compounds was determined. 相似文献