Bibliografías temáticas / Aminopropanone

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Literatura académica sobre el tema "Aminopropanone"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 1 de febrero de 2022

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Artículos de revistas sobre el tema "Aminopropanone"

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Fitzsimons, Mark F., M. Kamil Abdul Rashid, John P. Riley, and George A. Wolff. "Aminopropanone as a marker for raw sewage in natural waters." Marine Pollution Bulletin 30, no. 5 (1995): 306–12. http://dx.doi.org/10.1016/0025-326x(94)00177-b.

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Adia, Maqsood, Nadine Hénaff, and Andrew Whiting*. "An Unusual Rearrangement of N,N-Dibenzyl-2-aminopropanal to N,N-Dibenzyl-1-aminopropanone." Tetrahedron Letters 38, no. 17 (1997): 3101–2. http://dx.doi.org/10.1016/s0040-4039(97)00555-8.

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Forsch, Ronald, Henry Bader та Andre Rosowsky. "Synthesis of L-2-(N-Pteroylamino )-3-(N -phosphonoacetyl)aminopropanoic Acid as an Analogue of the Putative Phosphorylated Intermediate in the γ-Glutamation of Folic Acid by Folylpolyglutamate Synthetase". Pteridines 10, № 1 (1999): 39–46. http://dx.doi.org/10.1515/pteridines.1999.10.1.39.

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L-2-(N-Pteroyl)amino-3-(N-phosphonoacetyl)aminopropanoic acid was synthesized as an analogue of the putative y-phosphorylated intermediate in the enzyme-catalyzed γ-glutamation of folic acid by folylpolyglutamate synthetase (FPGS). N-(Benzyloxycarbonyl)-L-aspartic acid was converted in four steps to methyl L-2-(N-benzyloxycarbonyl)amino-3-aminopropanoate, and the latter was allowed to react with p-nitrophenyl dimethoxyphosphonoacetate to obtain methyl L-2-(N-benzyloxycarbonylamino)- 3-(N-dimethoxyphosphonoacetyl)aminopropanoate. After catalytic hydrogenation, the resulting amine was coupled to
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ADIA, M., N. HENAFF, and A. WHITING. "ChemInform Abstract: An Unusual Rearrangement of N,N-Dibenzyl-2-aminopropanal to N,N- Dibenzyl-1-aminopropanone." ChemInform 28, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.199733265.

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Singh, Simrat P., and Piero R. Gardinali. "Trace determination of 1-aminopropanone, a potential marker for wastewater contamination by liquid chromatography and atmospheric pressure chemical ionization–mass spectrometry." Water Research 40, no. 3 (2006): 588–94. http://dx.doi.org/10.1016/j.watres.2005.11.036.

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Sillanpää, Reijo, Teppo Lindgren, and Lassi Hiltunen. "Copper(II) complexes of 3-aminopropanols. Synthesis and structure of 3-aminopropanol(3-aminopropanolato)copper(II) iodide." Inorganica Chimica Acta 131, no. 1 (1987): 85–88. http://dx.doi.org/10.1016/s0020-1693(00)87911-6.

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Knabe, Joachim, and Wolfgang Buchheit. "Chirale 3-Aminopropanole, 2. Mitt. N-Alkylierungsprodukte." Archiv der Pharmazie 318, no. 8 (1985): 727–35. http://dx.doi.org/10.1002/ardp.19853180811.

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Li, Xiao Chuan, Shan Shan Gong, and Qi Sun. "Efficient Synthesis of Functionalized 3-Aminopropanols." Applied Mechanics and Materials 662 (October 2014): 67–70. http://dx.doi.org/10.4028/www.scientific.net/amm.662.67.

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A series of α-aminophosphonate-functionalized 3-aminopropanols have been efficiently prepared and characterized by1H,13C, and31P NMR and mass spectroscopy. The reaction conditions such as solvent and temperature were thoroughly investigated based on the three-component Kabachnik-Fields reaction. The experimental results revealed that moderate elevation of reaction temperature under solvent-free conditions was optimal for the synthesis of these types of compounds without forming the cyclized byproduct.
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9

Remko, Milan, and Martin Mackov. "Conformational structure of the antiarrhythmic mexiletine, its cation and hydrochloride." Collection of Czechoslovak Chemical Communications 55, no. 10 (1990): 2368–76. http://dx.doi.org/10.1135/cccc19902368.

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The PCILO and MNDO quantum chemical methods were applied to the conformational analysis of antiarrhythmic mexiletine 1-(2,6-dimethylphenoxy)-2-aminopropane, its cation and hydrochloride. The stable conformations, proton affinity, and the hydrogen bonding energy of the mexiletine ion pair were determined.
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10

Dudikova, D. M., Z. S. Suvorova, V. V. Nedashkivska, A. O. Sharova, M. L. Dronova, and N. O. Vrynchanu. "Antibiofilm activity of aminopropanol derivatives against Pseudomonas aeruginosa." Farmatsevtychnyi zhurnal, no. 1 (August 14, 2018): 93–100. http://dx.doi.org/10.32352/0367-3057.1.17.12.

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Bacterial biofilm, particularly formed by Pseudomonas aeruginosa, are a cause of severe chronic infectious diseases. Bacteria within a biofilm are phenotypically more resistant to antibiotics and the macroorganism immune system, making it an important virulence factor for many microbes.
 The aminopropanol derivatives with adamantyl (KVM-97) and N-alkylaryl radicals (KVM-194, KVM-204, KVM-261, and KVM-262) were used as study object. The aim of this study was to investigate the antibiofilm activity of compounds on biofilm formation and on mature biofilm of P. aeruginosa. The effects of the
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Tesis sobre el tema "Aminopropanone"

1

Williams, Michael Drummond. "Determination of oestrogens and aminoketones in urine and effluents using chromatographic and spectroscopic techniques." Thesis, University of the West of England, Bristol, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340816.

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Torres, Milton Daniel Aillon. "Sintese de 1 - aril - 2 - aminopropanos com possivel atividade simpatomimetica." reponame:Repositório Institucional da UFSC, 1990. http://repositorio.ufsc.br/xmlui/handle/123456789/75686.

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Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciencias Fisicas e Matematicas<br>Made available in DSpace on 2012-10-16T03:29:09Z (GMT). No. of bitstreams: 0Bitstream added on 2016-01-08T16:44:06Z : No. of bitstreams: 1 100044.pdf: 1193875 bytes, checksum: 127c649618779528f6a4936614e090b6 (MD5)<br>A estrutura da conhecida droga psicotomimética 1-(2,4,5-trimetoxifenil)-2-aminopropano (TMA-2) tem sido a base para múltiplas variações de substituintes que visam a uma melhor compreensão da ação alucinogênica das arilisopropilaminas no sistema nervoso central. Foram sinte
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Capítulos de libros sobre el tema "Aminopropanone"

1

Schomburg, Dietmar, and Dörte Stephan. "(R)-Aminopropanol dehydrogenase." In Enzyme Handbook 9. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-85200-8_72.

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Bährle-Rapp, Marina. "3-Aminopropane Sulfonic Acid." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_502.

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Winkelmann, Jochen. "Diffusion coefficient of 3-aminopropanoic acid in water." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_240.

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Winkelmann, Jochen. "Diffusion coefficient of 3-aminopropanoic acid in water at infinite dilution." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_1498.

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Winkelmann, Jochen. "Diffusion coefficient of tetrapropyl ammonium bromide into 3-aminopropanoic acid and water." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_2595.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with Schiff-base obtained from acetoacetic-2-pyridylamide and 3-aminopropanol." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_34.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) complex of Schiff base derived from 2, 6-diformyl-4-methylphenol and 1-aminopropane." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_132.

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"3-Selanyl-2-Aminopropanoic Acid." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_100004.

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9

"3-Selanyl-2-aminopropanoic Acid." In Encyclopedia of Systems Biology. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-9863-7_100012.

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10

"3-Selanyl-2-Aminopropanoic Acid." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_5047.

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