Academic literature on the topic 'Chloro benzaldehyde'

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Journal articles on the topic "Chloro benzaldehyde"

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Neamah, Rawaa, та Shaimaa Adnan. "Study the Biological Activity for Shiff Base and Β – Lactam Compounds that Synthesis and Identification from Pyrimidine Derivatives". International Journal of Pharmaceutical Quality Assurance 11, № 01 (2013): 37–39. http://dx.doi.org/10.25258/ijpqa.11.1.12.

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In This study We are synthesis and characterization of some Schiff base and β- lactam derivatives) by three steps. The First react 2-amino-4-Chloro-6-methyl pyrimidine with 4-amino acetophenone in an acid medium to get shiff base derivative(E)-4-(1-((4-Chloro-6-methyl pyridine-2-yl)imino)ethyl)aniline (1), the second step (1) react with (3,4- dimethoxybenzal dehyde,4-methyl benzaldehyde,4-dimethylamino benzaldehyde,4-bromo benzaldehyde,4–hydroxy benzaldehyde, 4-Nitro benzaldehyde) to get Schiff base derivatives (2-7), the last step (2-7) derivatives react with Chloro acetyl chloride to get –β-
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Li, Yong-Fei, Can-Cheng Guo, Xu-Hui Yan, and Qiang Liu. "Aerobic oxidative cleavage of C=C double bond of styrene catalyzed by simple manganese porphyrin." Journal of Porphyrins and Phthalocyanines 10, no. 07 (2006): 942–47. http://dx.doi.org/10.1142/s1088424606000260.

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The aerobic oxidative cleavage of styrene C=C double bonds catalyzed by simple manganese porphyrin is reported. Under the catalysis of chloro(tetraphenylporphinato)manganese, the oxidative cleavage of the carbon-carbon double bond of the styrene with air yields benzaldehyde. Our results show that the oxidative cleavage and the epoxidation of the styrene double bond are the competition reactions in the styrene-manganese porphyrin-air system. The reaction temperature decided the product distribution. Under the conditions of 0.4 MPa air and 30 ppm of chloro(tetraphenylporphinato)manganese, the st
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Ramesh, Baboo. "Ru (III) Catalysed Oxidative Degradation of Sodium Bisulphite Derivatives of Aromatic Aldehydes by Potassium Hexacyano Ferrate (III) in Aqueous Alkaline Medium." International Journal of Current Research and Review 14, no. 19 (2022): 17–20. http://dx.doi.org/10.31782/ijcrr.2022.141903.

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Introduction: The catalysed oxidation of the derivatives of aromatic aldehydes with inorganic moieties is still unstudied with an economically cheaper oxidant like potassium hexacyanoferrate (III). The catalyst like ruthenium (III) chloride is very much effective at very low concentrations for oxidation reactions. Aims: The study is carried out to observe and to get the results about the oxidative degradation of derivatives of organic and inorganic moieties. Methodology: Benzaldehyde sodium bisulphite (BSS) and substituted aromatic aldehyde sodium bi sulphite like p-chloro benzaldeyde sodium b
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Jayashree, B. S., Gurushyam Sri, and A. Pai. "SYNTHESIS, CHARACTERISATION, ANTIOXIDANT AND ANTICANCER EVALUATION OF NOVEL FLAVONE-4-OXIMES." INDIAN DRUGS 54, no. 11 (2017): 7–14. http://dx.doi.org/10.53879/id.54.11.11170.

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A series of novel flavone-4-oximes were synthesized by the oximation of substituted flavones. The synthesized compounds were characterized by various spectrochemical methods including IR, MS and NMR spectroscopy. Out of the 14 test compounds screened for their antioxidant activity, compounds such as JGS-VI (a N,N dimethyl benzaldehyde derivative) and JGS-VII (a 3,4 dimethoxy benzaldehyde derivative) exhibited antioxidant activity comparable to that of ascorbic acid and quercetin as standards following DPPH method. Compounds such as JGS-II (a p-fluoro benzaldehyde derivative), JGS-IV (a p-methy
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Hania, Majed M. "Synthesis and Antibacterial Activity of Some Transition Metal Complexes of Oxime, Semicarbazone and Phenylhydrazone." E-Journal of Chemistry 6, s1 (2009): S508—S514. http://dx.doi.org/10.1155/2009/204714.

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Co, Ni and Cu complexes have been prepared by reacting metal chloride with 4-chlorobenzaldehyde oxime, 4-methylbenzaldehyde oxime, 4-nitrobenzaldehyde oxime, 4-chlorobenzaldehyde semicarbazone, 4-methyl- benzaldehyde semicarbazone, 4-nitrobenzaldehyde semicarbazone, 4-chloro benzaldehyde phenylhydrazone, 4-methylbenzaldehyde phenyl hydrazone and 4-nitrobenzaldehyde phenylhydrazone and their antibacterial activity have been studied and compared with their ligands againstE. coliwhich gave significant results of activity.
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Mulya, Putri Widya, Jumina, Dwi Siswanta, and Budiana I. M. Gusti Ngurah. "Synthesis of C-2-Ethoxycarbonylmethoxyphenyl Calix[4]Resorcinarene Using Salicylaldehyde as Basic Material and its Application as Adsorbent of Pb(II) Metal Cation." Advanced Materials Research 1043 (October 2014): 129–32. http://dx.doi.org/10.4028/www.scientific.net/amr.1043.129.

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Synthesis of C-2-ethoxycarbonylmethoxyphenyl calix [4] resorcinarene and its application for adsorption of Pb (II) metal cation have been carried out. C-2-ethoxycarbonylmethoxyphenyl calix [4] resorsinarene was produced in three steps i.e (1) esterification of 2-chloro acetic acid, (2) reaction ethyl 2-chloro acetate with salicylaldehide in to yield 2-ethoxycarbonylmethoxy benzaldehyde, and (3) reaction 2-ethoxycarbonylmethoxy benzaldehyde with resorcinol in acidic condition to yield C-2-ethoxycarbonylmethoxyphenyl calix [4] resorcinarene. The prepared compounds were characterized by FTIR, 1H-
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Abd alazez, Enas k., Ayad M. R. Raauf, and Karima F. Ali. "Synthesis, Characterization and Antibacterial Activity of New Derivatives of Imidazolidine having Sulfamethoxazole Moiety." Al Mustansiriyah Journal of Pharmaceutical Sciences 19, no. 4 (2019): 217–38. http://dx.doi.org/10.32947/ajps.v19i4.655.

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This work includes Synthesis of new series of sulfa drugs derived from sulfamethoxazole containing substituted Imidazolidine moiety. These compounds expected to have antibacterial activity, due to their Imidazolidine moiety This work includes synthesis of some new
 Schiff bases (II1-5) by condensation of sulfamethoxazole drug(I) with some aldehydes (1-5) (benzaldehyde, p-chloro benzaldehyde, p-nitro benzaldehyde, p-hyroxy benzaldehyde and p-N, N-dimethyl amino benzaldehyde). These Schiff bases were found to react with glycine, to prepared new imidazolidine derivatives (III1-5). The prepar
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Cambie, RC, JM Coddington, JBJ Milbank, et al. "Stereoselective Titanium-Mediated Aldol Reactions of Menthyl Acetate Enolates, and Allylations With Benzaldehyde." Australian Journal of Chemistry 46, no. 5 (1993): 583. http://dx.doi.org/10.1071/ch9930583.

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The enolates of (+)- and (-)- menthyl acetate, formed by transmetallation from lithium with chloro ( cyclopentadienyl )bis(1,2:5,6-di-O-isopropylidene-α-D-glucofuranosato-O3)titanium [ CpTi (DAGO)2Cl] (1), react with benzaldehyde from the Re-face with high stereoselectivities (95 and 92% diastereomeric excess) when 12-crown-4 is used during the transmetallation . Use of the chiral cyclopentadienyltitanium-α,α,αα,αα-tetraaryl-2,2-dimethyl-1,3-dioxolan-4,5-dimethanol (TADDOL) complex (3) gives lower diastereoselectivities (58 and 40%) but the Si -face of benzaldehyde is attacked preferentially.
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R., Behal, Sharma S., Bansal T., Gaba J., and Kaur S. "Synthesis of a series of new Schiff bases having heterocyclic moiety and their microbial activity." Journal of Indian Chemical Society Vol. 96, Mar 2019 (2019): 349–54. https://doi.org/10.5281/zenodo.5650942.

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Department of Chemistry, Department of Plant Breeding and Genetics, Punjab Agricultural University, Ludhiana-141 004, Punjab, India <em>E-mail</em>: radhikabehal19@yahoo.com, sunita_sharma@pau.edu, taniabansal2@yahoo.com, jyotgcw@gmail.com, kaur.sandeep18@gmail.com <em>Manuscript received online 05 September 2018, revised 20 February 2019, accepted 26 February 2019</em> Heterocyclic compounds were synthesized using water based method. These were synthesized by reacting different aldehydes namely benzaldehyde, 2-chloro benzaldehyde, 4-chloro benzaldehyde, 2-nitro benzaldehyde and 3-nitro benzal
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Amal S. Sadiq. "Synthesis of N-Substituted 3-Chloro- 2-azetidinones for 2, 4-diamino-6- hydroxy pyrimidin." Journal of the College of Basic Education 21, no. 88 (2023): 13–24. http://dx.doi.org/10.35950/cbej.v21i88.9949.

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This search involved synthesis of several new N-Substituted -3-chloro-&#x0D; 2-azetidinones which were known as a high medicinal effectiveness for 2,&#x0D; 4-Diamino-6-hydroxy pyrimidin in two steps. The first step included&#x0D; preparation Shiff bases (1-6) by condensation of 2, 4-Diamino-6-hydroxy&#x0D; pyrimidin with many substituted aldehydes(4-hydroxy benzaldehyde, 2-&#x0D; bromobenzaldehyde, 4-dimethyl amino benzaldehyde, = 4-nitro&#x0D; benzaldehyde, salicylaldehyde, 4-chlorobenzaldehyde), then the second&#x0D; step included, preparation new six azetidinones compounds (7-12) by&#x0D; r
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Dissertations / Theses on the topic "Chloro benzaldehyde"

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Huser, Marc. "Carbonylations catalytiques du chlorobenzene et du dichloromethane." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13196.

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Book chapters on the topic "Chloro benzaldehyde"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of chloro-4-(2-pyridyl)-1-(2, 4-dihydroxy- benzaldehyde)- 3-thiosemicarbazonatomanganese(II)." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_631.

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