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Relevant bibliographies by topics / Para-substituted benzyl chlorides

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Academic literature on the topic 'Para-substituted benzyl chlorides'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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Journal articles on the topic "Para-substituted benzyl chlorides"

1

Bijudas, K., and P. Bashpa. "Selective Oxidation of Benzyl Halides to Benzaldehydes by Phase Transfer Catalyzed Monochromate Ions in Non-Polar Solvents." Asian Journal of Organic & Medicinal Chemistry 5, no. 3 (2020): 249–53. http://dx.doi.org/10.14233/ajomc.2020.ajomc-p287.

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Benzyl chloride, benzyl bromide and their para substituted derivatives were selectively oxidized to corresponding benzaldehydes by acidified monochromate in toluene and ethyl acetate with the help of phase transfer catalysts like tetrabutylphosphonium bromide (TBPB), tetrabutylammonium bromide (TBAB), tetrabutylammonium hydrogen sulphate (TBAHS), cetyltrimethylammonium bromide (CTMAB) and tricaprylmethylammonium chloride (TCMC). The reaction was carried out by simple magnetic stirring for about 2 h at 60 ºC. The products were recrystallized and analyzed by infrared and UV-visible spectral tech

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2

Lee, Ikchoon, Dae Dong Sung, Tae Seop Uhm, and Zoon Ha Ryu. "Methanolyses of para-substituted benzoyl chlorides in isodielectric binary mixtures." Journal of the Chemical Society, Perkin Transactions 2, no. 11 (1989): 1697. http://dx.doi.org/10.1039/p29890001697.

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3

Danihel, Ivan, Ján Imrich, Dušan Košťík, Pavol Kristian, and Gabriela Barančíková. "13C NMR spectra and substituent effects of meta and para substituted benzoyl isothiocyanates." Collection of Czechoslovak Chemical Communications 50, no. 6 (1985): 1422–31. http://dx.doi.org/10.1135/cccc19851422.

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13C NMR spectra have been studied of 20 meta and para substituted benzoyl isothiocyanates and corresponding benzoyl chlorides. The 13C SCS values of the carbon atom in NCS group have been found to correlate linearly with the Hammet σm,p constants of the substituents as well as with the corresponding π electron charges. The 13C SCS (substituent chemical shift) values of the carbonyl carbon atom of the compounds investigated are little sensitive to substituent effects and are analyzed on the basis of the dual-substituent-parameter approach. Also discussed are the intercorrelation relations of th

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4

Bentley, T. William, and H. Carl Harris. "Solvolyses of para-substituted benzoyl chlorides in trifluoroethanol and in highly aqueous media." Journal of the Chemical Society, Perkin Transactions 2, no. 4 (1986): 619. http://dx.doi.org/10.1039/p29860000619.

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Bauerová, Ingrid, and Miroslav Ludwig. "Substituent Effects on the Base-Catalysed Hydrolysis of Phenyl Esters of para-Substituted Benzoic Acids." Collection of Czechoslovak Chemical Communications 65, no. 11 (2000): 1777–90. http://dx.doi.org/10.1135/cccc20001777.

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Seventeen model phenyl esters of 4-substituted benzoic acids were synthesised by the reaction of substituted benzoyl chlorides with phenol in aqueous alkaline solutions (Schotten-Baumann reaction), in pyridine (Einhorn reaction), or by the reaction of substituted benzoic acids with phosphorus oxychloride. Structures and purity of the model compounds were confirmed by 1H NMR and 13C NMR spectroscopy as well as by HPLC and elemental analysis. Phenyl 4-aminobenzoate was synthesised by reduction of phenyl 4-nitrobenzoate in methanol on palladium. Kinetics of base-catalysed hydrolysis of model phen

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6

Anupam, Anupam, Mohammed Al-Bratty, Hassan Ahmad Alhazmi, et al. "Synthesis and biological evaluation of triphenyl-imidazoles as a new class of antimicrobial agents." European Journal of Chemistry 9, no. 4 (2018): 369–74. http://dx.doi.org/10.5155/eurjchem.9.4.369-374.1785.

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Newer triphenyl-imidazole derivatives (4a-h) were synthesized in good yields by the reaction of benzil and substituted benzaldehydes in equimolar quantities and refluxing the product with acetyl chloride thereafter. Structures were confirmed by using FT-IR, 1H NMR and 13C NMR spectroscopic methods. All the synthesized compounds were tested for their antimicrobial activity using agar diffusion technique against Gram positive (Staphhylococcus aureus and Bacillus subtilis), Gram negative (Escherichia coli and Pseudomonas aureginosa) as well as Fungal strain (Candida albicans). Interestingly compo

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7

LEE, I., D. D. SUNG, T. S. UHM, and Z. H. RYU. "ChemInform Abstract: Methanolyses of para-Substituted Benzoyl Chlorides in Isodielectric Binary Mixtures." ChemInform 21, no. 10 (1990). http://dx.doi.org/10.1002/chin.199010071.

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8

BENTLEY, T. W., and H. C. HARRIS. "ChemInform Abstract: Solvolyses of para-Substituted Benzoyl Chlorides in Trifluoroethanol and in Highly Aqueous Media." Chemischer Informationsdienst 17, no. 31 (1986). http://dx.doi.org/10.1002/chin.198631118.

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Dissertations / Theses on the topic "Para-substituted benzyl chlorides"

1

MacMillar, Susanna. "Isotopes as Mechanism Spies : Nucleophilic Bimolecular Substitution and Monoamine Oxidase B Catalysed Amine Oxidation Probed with Heavy Atom Kinetic Isotope Effects." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis (AUU), 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7441.

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Books on the topic "Para-substituted benzyl chlorides"

1

Koerner, Terry. Using kinetic isotope effects to model the transition states for the sn2 reactions between sodium borohydride and para-substituted benzyl chlorides. Laurentian University Press, 1996.

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