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901.
Dr. Ivan Halasz Andreas Puškarić Dr. Simon A. J. Kimber Patrick J. Beldon Dr. Ana M. Belenguer Frank Adams Dr. Veijo Honkimäki Prof. Robert E. Dinnebier Bhavnita Patel Prof. William Jones Dr. Vjekoslav Štrukil Prof. Tomislav Friščić 《Angewandte Chemie (International ed. in English)》2013,52(44):11665-11665
902.
The objective of this research is to utilize a new poly[N,N-diallyl pyrrolidinium bromide-co-N,Ndimethyl acrylamide-co-acrylic acid sodium salt]superabsorbent hydrogel(SAH)for the removal of two anionic dyes,e.g.,Reactive Red 5B(RR5B)and Reactive Orange M2R(ROM2R),from water.The SAH was characterized by swelling in water,FTIR,TGA and SEM.The SAH DDA6showed good swelling property and thermal stability.We have also investigated the parameters affecting dye adsorption such as pH,adsorbent dose,adsorption rate and initial dye concentration.The experimental data were also analyzed by applying the well known Langmuir and Freundlich isotherm models. 相似文献
903.
A new series of pyrido[1,2-α]benzimidazole derivatives bearing the aryloxypyrazole nucleus have been synthesized by base-catalyzed cyclocondensation reaction through multi-component reaction(MCR) approach.All the synthesized compounds were investigated against a representative panel of pathogenic strains using broth microdilution minimum inhibitory concentration(MIC) method for their in vitro antimicrobial activity.Reviewing the data,majority of the compounds were found to be active against employed pathogens.SAR study explores that antimicrobial activity is strongly depends on the nature of the substituents at the ether linked aryl ring attached to the pyrazole unit,together with the substituent present on the C5 of the benzimidazole unit. 相似文献
904.
Neal J. Fazakerley Dr. Matthew D. Helm Prof. David J. Procter 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(21):6718-6723
The first enantiospecific total synthesis of the antibacterial natural product (+)‐pleuromutilin has been achieved. The approach includes the synthesis of a non‐racemic cyclisation substrate from (+)‐trans‐dihydrocarvone, a highly selective SmI2‐mediated cyclisation cascade, an electron transfer reduction of a hindered ester, and the first efficient conversion of (+)‐mutilin to the target. 相似文献
905.
Anju Chopra Dheer Singh R. Manna S. Saravanan M. I. S. Sastry M. B. Patel B. Basu 《Chromatographia》2014,77(11-12):845-851
A GC and IR based protocol was developed for monitoring the isobutene dimerisation process wherein the complete characterisation of the products was carried out by GC coupled with mass spectrometry. In the dimerisation process, LPG from FCC process comprising a mixture of saturated and unsaturated C4 hydrocarbons is subjected to a dimerisation process using a catalyst to produce C8 hydrocarbons. The reaction is carried out keeping in view the demand for high-octane blending components in gasoline. The isooctene generated in the process (mainly from the dimerisation of isobutene) is converted into isooctane having the RON and MON value 100. The monitoring process requires the use of two different column chemistries, viz., a 100 m CPSIL PONA CB non-polar column for C8 and its isomers and an Alumina PLOT column for C4 hydrocarbons. A 100 m non-polar column does not separate the C4 mixture since the column is meant for gasoline range products containing C5 and above hydrocarbons. Therefore, a need was felt for an improvised method which can handle both the analyses simultaneously. A cryogenic oven program starting from 0 °C was developed for separating the isomers of C4 hydrocarbons and C8 hydrocarbons on a single column during the single run by Detailed Hydrocarbon Analyzer. The data obtained using the cryo programme was validated with data obtained using Alumina PLOT column on C4 mixture since the Alumina PLOT column is the widely accepted column chemistry for separating the C4 hydrocarbons. An IR method for the estimation of the total olefin content was developed using 2,2,4-trimethyl pentene-1 as the reference standard. The total olefins generated during the process were identified by GC–MS, quantified by DHA-FID and validated by infrared spectroscopy. A good correlation was found between GC and IR spectral results (correlation coefficient R 2 = 0.99). 相似文献
906.
Satish S. More Akula Raghunadh Ramanathan Shankar Navin B. Patel Dinesh S. Bhalerao Unniaran K. Syam Kumar 《Helvetica chimica acta》2014,97(3):404-413
The first total synthesis of the α‐oxo amide‐based natural product, N‐(3‐guanidinopropyl)‐2‐(4‐hydroxyphenyl)‐2‐oxoacetamide ( 3 ), isolated from aqueous extracts of hydroid Campanularia sp., has been achieved. The α‐oxo amide 12 , prepared via the oxidative amidation of 1‐[4‐(benzyloxy)phenyl]‐2,2‐dibromoethanone ( 9a ) with 4‐{[(tert‐butyl)(dimethyl)silyl]oxy}butan‐1‐amine ( 10a ), has been used as the key intermediate in the total synthesis of 3 as HBr salt. On the way, an expeditious total synthesis of polyandrocarpamide C ( 2c ), isolated from marine ascidian Polyandrocarpa sp., was carried out in four steps. 相似文献
907.
Synthesis and In Vitro Antimicrobial Screening of New Azetidin‐2‐ones of 5‐Ethyl Pyridine‐2‐ethanol
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Navin B. Patel Hemant R. Patel Faiyazalam M. Shaikh Dhanji Rajani 《Journal of heterocyclic chemistry》2014,51(3):775-787
A new series of azetidinones is described in this paper; Schiff base ( 4a , 4b , 4c , 4d , 4e , 4f , 4g , 4h , 4i , 4j , 4k , 4l , 4m , 4n , 4o ) were synthesized from 4‐[2‐(5‐ethylpyridin‐2‐yl)ethoxy]benzaldehyde, which was used to synthesize azetidinones ( 5a , 5b , 5c , 5d , 5e , 5f , 5g , 5h , 5i , 5j , 5k , 5l , 5m , 5n , 5o ), ( 6a , 6b , 6c , 6d , 6e , 6f , 6g , 6h , 6i , 6j , 6k , 6l , 6m , 6n , 6o ), and ( 7a , 7b , 7c , 7d , 7e , 7f , 7g , 7h , 7i , 7j , 7k , 7l , 7m , 7n , 7o ). The structures of the synthesized compounds were assigned on the basis of elemental analysis, IR, 1H NMR, and 13C NMR spectral data. All the products were screened against different strains of bacteria and fungi. Most of the monosubstituted and disubstituted chloro groups are more effective to both bacterial and fungal species in comparison with the standard drugs. 相似文献
908.
909.
Ajit Patel 《Journal of Applied Mathematics and Computing》2011,37(1-2):37-56
The basic requirement for the stability of the mortar element method is to construct finite element spaces which satisfy certain criteria known as inf-sup (well known as LBB, i.e., Ladyzhenskaya-Babu?ka-Brezzi) condition. Many natural and convenient choices of finite element spaces are ruled out as these spaces may not satisfy the inf-sup condition. In order to alleviate this problem Lagrange multiplier method with penalty is used in this paper. The existence and uniqueness results of the discrete problem are discussed without using the discrete LBB condition. We have also analyzed the Lagrange multiplier method with penalty for parabolic initial-boundary value problems using semidiscrete and fully discrete schemes. We have derived sub-optimal order of estimates for both semidiscrete and fully discrete schemes. The results of numerical experiments support the theoretical results obtained in this article. 相似文献
910.