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1.
Kalagouda?B.?GudasiEmail author Ramesh?S.?Vadavi Rashmi?V.?Shenoy Manjula?S.?Patil Siddappa?A.?Patil Munirathinam?Nethaji 《Transition Metal Chemistry》2005,30(6):661-668
The synthesis of cobalt(II), nickel(II) and zinc(II) complexes of 2-pyridine-2-yl-3(pyridine-2-carboxylideneamino)-1,2-dihydroquinazolin-4(3H)-one is described. The ligand and metal complexes were characterized by elemental analysis, conductivity measurements, spectral (u.v.–vis., i.r., 1D n.m.r., 2D hetcor and mass) and thermal studies. The cobalt(II) complex crystallizes as pink crystals in the monoclinic crystal system, space group P21/n with a = 10.066(6) Å, b = 15.929(9) Å, c = 12.624(7) Å, α = 90.00(9)°, β = 110.850 (8)°, γ = 90.00, V = 1891.5 (18) Å3 and Z = 4. The geometry around the cobalt atom is distorted trigonal bipyramidal with τ = 0.83 [structural parameter, τ = (β − α)/60; where α and β are the two basal angles in a five coordinate complex]. 相似文献
2.
Magnetic nanoparticle‐tethered Schiff base–palladium(II): Highly active and reusable heterogeneous catalyst for Suzuki–Miyaura cross‐coupling and reduction of nitroarenes in aqueous medium at room temperature 下载免费PDF全文
K. Manjunatha Tuhin S. Koley Vishal Kandathil Ramesh B. Dateer Geetha Balakrishna B. S. Sasidhar Shivaputra A. Patil Siddappa A. Patil 《应用有机金属化学》2018,32(4)
As a continuation of our efforts to develop new heterogeneous nanomagnetic catalysts for greener reactions, we identified a Schiff base–palladium(II) complex anchored on magnetic nanoparticles (SB‐Pd@MNPs) as a highly active nanomagnetic catalyst for Suzuki–Miyaura cross‐coupling reactions between phenylboronic acid and aryl halides and for the reduction of nitroarenes using sodium borohydride in an aqueous medium at room temperature. The SB‐Pd@MNPs nanomagnetic catalyst shows notable advantages such as simplicity of operation, excellent yields, short reaction times, heterogeneous nature, easy magnetic work up and recyclability. Characterization of the synthesized SB‐Pd@MNPs nanomagnetic catalyst was performed with various physicochemical methods such as attenuated total reflectance infrared spectroscopy, UV–visible spectroscopy, inductively coupled plasma atomic emission spectroscopy, energy‐dispersive X‐ray spectroscopy, field‐emission scanning electron microscopy, transmission electron microscopy, powder X‐ray powder diffraction, thermogravimetric analysis and Brunauer–Emmett–Teller surface area analysis. 相似文献
3.
Siddappa Patil Anthony Deally Brendan Gleeson Helge Müller‐Bunz Francesca Paradisi Matthias Tacke 《应用有机金属化学》2010,24(11):781-793
From the reaction of 1H‐imidazole ( 1a ), 4,5‐dichloro‐1H‐imidazole ( 1b ) and 1H‐benzimidazole ( 1c ) with p‐cyanobenzyl bromide ( 2 ), symmetrically substituted N‐heterocyclic carbene (NHC) [( 3a–c )] precursors, 1‐methylimidazole ( 5a ), 4,5‐dichloro‐1‐methylimidazole ( 5b ) and 1‐methylbenzimidazole ( 5c ) with benzyl bromide ( 6 ), non‐symmetrically substituted N‐heterocyclic carbene (NHC) [( 7a–c )] precursors were synthesized. These NHC? precursors were then reacted with silver(I) acetate to yield the NHC‐silver complexes [1,3‐bis(4‐cyanobenzyl)imidazole‐2‐ylidene] silver(I) acetate ( 4a ), [4,5‐dichloro‐1,3‐bis(4‐cyanobenzyl)imidazole‐2‐ylidene] silver(I) acetate ( 4b ), [1,3‐bis(4‐cyanobenzyl)benzimidazole‐2‐ylidene] silver(I) acetate ( 4c ), (1‐methyl‐3‐benzylimidazole‐2‐ylidene) silver(I) acetate ( 8a ), (4,5‐dichloro‐1‐methyl‐3‐benzylimidazole‐2‐ylidene) silver(I) acetate ( 8b ) and (1‐methyl‐3‐benzylbenzimidazole‐2‐ylidene) silver(I) acetate ( 8c ) respectively. The four NHC‐precursors 3a–c, 7c and four NHC–silver complexes 4a–c and 8c were characterized by single crystal X‐ray diffraction. The preliminary antibacterial activity of all the compounds was studied against Gram‐negative bacteria Escherichia coli, and Gram‐positive bacteria Staphylococcus aureus using the qualitative Kirby‐Bauer disc‐diffusion method. All NHC–silver complexes exhibited medium to high antibacterial activity with areas of clearance ranging from 4 to 12 mm at the highest amount used, while the NHC‐precursors showed significantly lower activity. In addition, all NHC–silver complexes underwent preliminary cytotoxicity tests on the human renal‐cancer cell line Caki‐1 and showed medium to high cytotoxicity with IC50 values ranging from 53 ( ± 8) to 3.2 ( ± 0.6) µM. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
4.
Zusammenfassung Verschiedene, brom-, chlor-, dichlor-, brommethoxy- und phenylsubstituierte 2-Hydroxy-4-azachalkone wurden durch basenkatalysierte Kondensation geeigneter o-Hydroxy-acetophenone mit Pyridin-4-aldehyd hergestellt und in die entsprechenden 4-Azaflavone, 4-Azaflavonole und 4-Azaflavanone umgewandelt.
Several bromo-, chloro-, dichloro-, bromomethoxy- and phenylsubstituted 2-hydroxy-4-azachalcones have been prepared by base catalyzed condensation of the appropriate o-hydroxyacetophenones with 4-pyridinealdehyde, and subsequently converted into the corresponding 4-azaflavones, 4-azaflavonols and 4-azaflavanones.相似文献
5.
Miss K. H. Sinnur G. R. Revankar S. Siddappa 《Monatshefte für Chemie / Chemical Monthly》1966,97(2):417-422
Zusammenfassung Eine Reihe von Hydroxybenzylbenzimidazolen wurde durch Kondensation verschiedener aromatischer o-Diamine mit Brommandelsäuren unter Verwendung von 6n-HCl als Kondensationsmittel hergestellt. Für die Substituenten in der Benzolhälfte wurden die Stellungen 4(7)-, 5(6)-, 5,6- oder 4,6(5,7)- ge-wählt; der Phenylrest der Hydroxybenzylhälfte trägt ein Bromatom in der o- oder p-Stellung. Die Darstellung der o-Brom-mandelsäure wird beschrieben.
A series of hydroxybenzylbenzimidazoles has been synthesized by condensing various aromatic o-diamines with bromomandelic acids using 6 N hydrochloric acid as condensing agent. o-Phenylene diamines to yield benzimidazoles substituted at positions 4(7)-, 5(6)- or 4,6(5,7)- were selected; the phenyl group of the hydroxybenzyl moiety carries a bromo substituent in the o- or p-position. The preparation of o-bromomandelic acid is described in some detail.相似文献
6.
7.
Vikrant Patil Enrique Barragan Shivaputra A. Patil Siddappa A. Patil Alejandro Bugarin 《Tetrahedron letters》2017,58(35):3474-3477
A series of new chlorinated thiabendazoles (6a–m) have been synthesized from readily available anilines and 4-cyanothiazole in moderate to good yields. All synthesized compounds were fully characterized using 1H NMR, 13C NMR, IR, and mass spectrometry. Additionally, the structure of the compound (6f) was confirmed by single-crystal X-ray diffraction. In addition, synthesis of 2-substituted benzimidazoles and 2-phenyl benzothiazole was investigated using our optimized conditions and the outcome is presented herein. 相似文献
8.
Siddappa Patil Karolin Dietrich Anthony Deally Brendan Gleeson Helge Müller‐Bunz Francesca Paradisi Matthias Tacke 《Helvetica chimica acta》2010,93(12):2347-2364
From the reaction of 1H‐imidazole ( 1a ), 4,5‐dichloro‐1H‐imidazole ( 1b ), 1H‐benzimidazole ( 1c ), 1‐methyl‐1H‐imidazole ( 1d ), and 1‐methyl‐1H‐benzimidazole ( 1f ) with methyl 4‐(bromomethyl)benzoate ( 2 ), symmetrically and nonsymmetrically 4‐(methoxycarbonyl)benzyl‐substituted N‐heterocyclic carbene (NHC) precursors, 3a – 3f , were synthesized. These NHC precursors were then reacted with silver(I) acetate (AgOAc) to yield the NHC–silver acetate complexes (acetato‐κO){1,3‐bis[4‐(methoxycarbonyl)benzyl]imidazol‐2‐ylidene}silver ( 4a ), (acetato‐κO){4,5‐dichloro‐1,3‐bis[4‐(methoxycarbonyl)benzyl]‐2,3‐dihydro‐1H‐imidazol‐2‐yl}silver ( 4b ), (acetato‐κO){1,3‐bis[4‐(methoxycarbonyl)benzyl]‐2,3‐dihydro‐1H‐benzimidazol‐2‐yl}silver ( 4c ), (acetato‐κO){1‐[4‐(methoxycarbonyl)benzyl]‐3‐methyl‐2,3‐dihydro‐1H‐imidazol‐2‐yl}silver ( 4d ), (acetato‐κO){4,5‐dichloro‐1‐[4‐(methoxycarbonyl)benzyl]‐3‐methyl‐2,3‐dihydro‐1H‐imidazol‐2‐yl}silver ( 4e ), and (acetato‐κO){1‐[4‐(methoxycarbonyl)benzyl]‐3‐methyl‐2,3‐dihydro‐1H‐benzimidazol‐2‐yl}silver ( 4f ), respectively. The three NHC–AgOAc complexes 4a, 4c , and 4d were characterized by single‐crystal X‐ray diffraction. All compounds studied in this work were preliminarily screened for their antimicrobial activities in vitro against Gram‐positive bacteria Staphylococcus aureus, and Gram‐negative bacteria Escherichia coli using the qualitative disk‐diffusion method. All NHC–AgOAc complexes exhibited weak‐to‐medium antibacterial activity with areas of clearance ranging from 4 to 7 mm at the highest amount used, while the NHC precursors showed significantly lower activity. In addition, NHC–AgOAc complexes 4a and 4b , and 4d – 4f exhibited in preliminary cytotoxicity tests on the human renal‐cancer cell line Caki‐1 medium‐to‐high cytotoxicities with IC50 values ranging from 3.3±0.4 to 68.3±1 μM . 相似文献
9.
Chandrappa Siddappa 《Tetrahedron letters》2010,51(50):6493-6497
A one-pot synthesis of benzimidazoles from gem-dibromomethylarenes is described. The reaction shows the method to prepare a variety of benzimidazole analogues with excellent yield. 相似文献
10.
Madhusudana Reddy M. Bhojegowd Ashoka Siddaramanna Anandakumar B. Siddappa Chandrappa G. Thimmanna Mohamed A. Pasha 《中国化学》2011,29(9):1863-1868
Nanocrystalline zirconium(IV) oxide (nc‐ZrO2) possessing high surface area was synthesized by a low temperature eco‐friendly solution combustion method using a new organic fuel alanine. The powder XRD, SEM and surface area measurements were carried out for characterization of nc‐ZrO2. The powder XRD results revealed that, the nc‐ZrO2 has the pure tetragonal phase. The crystallite size calculated by Scherrer's formula and BET surface area were found to be ca. 53–57 nm and ca. 275 m2/g, respectively. SEM micrograph exhibited the macroporous nature of the powder. nc‐ZrO2 has been employed as a catalyst for the solvent‐free synthesis of 3,4‐dihydro‐ pyrimidin‐2‐ones (DHPMs) by a microwave (MW) assisted one‐pot, multicomponent Biginelli condensation reaction of araldehydes, ethylacetoacetate and urea or thiourea. DHPMs are obtained in good to excellent yields (85%–96%) under this reaction condition within short interval of time (10–20 min). 相似文献