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Journal articles on the topic 'Aminopropanone'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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11

Antelo, Juan M., Florencio Arce, Julia Franco, P. Rodriguez Barro, and Angel Varela. "Stability ofN-chloro-3-aminopropanol in aqueous solution. Kinetics of decomposition and disproportion ofN-chloro-3-aminopropanol." International Journal of Chemical Kinetics 21, no. 5 (1989): 343–54. http://dx.doi.org/10.1002/kin.550210505.

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12

Boeckh, Jürgen, Heinz Breer, Martin Geier, et al. "Acylated 1,3-Aminopropanols as Repellents against Bloodsucking Arthropods." Pesticide Science 48, no. 4 (1996): 359–73. http://dx.doi.org/10.1002/(sici)1096-9063(199612)48:4<359::aid-ps490>3.0.co;2-z.

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13

Khalil, Andrew S., and Richard J. Lavrich. "Intramolecular hydrogen bond stabilized conformation of 3-aminopropanol." Journal of Molecular Spectroscopy 370 (April 2020): 111279. http://dx.doi.org/10.1016/j.jms.2020.111279.

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14

Dandia, Anshu, Meha Sati, Sangeeta Sanan, and R. Joshi. "REACTIONS OF INDOLE-2,3-DIONES WITH 3-AMINOPROPANOL." Organic Preparations and Procedures International 35, no. 4 (2003): 433–38. http://dx.doi.org/10.1080/00304940309355857.

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15

Thomsen, Ditte L., Jessica L. Axson, Sidsel D. Schrøder, Joseph R. Lane, Veronica Vaida, and Henrik G. Kjaergaard. "Intramolecular Interactions in 2-Aminoethanol and 3-Aminopropanol." Journal of Physical Chemistry A 117, no. 40 (2013): 10260–73. http://dx.doi.org/10.1021/jp405512y.

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16

Thompson, Hannah R., Hannah C. Masri, and Steven Stevenson. "Aminopropanol–xylene to chemically purify Gd3N@C88 metallofullerene." Inorganica Chimica Acta 468 (November 2017): 177–82. http://dx.doi.org/10.1016/j.ica.2017.04.020.

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17

Hauer, Jan, and Jan Šebenda. "Preparation and polymerization of 3-(2-adamantyl)-3-methyl-2-azetidinone." Collection of Czechoslovak Chemical Communications 50, no. 2 (1985): 454–58. http://dx.doi.org/10.1135/cccc19850454.

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3-(2-Adamantyl)-3-methyl-2-azetidinone (VI) was prepared, and new compounds, namely, methyl 2-(2-adamantyl) cyanoacetate, methyl-2-(2-adamantyl)-2-cyanopropanoate and methyl-2-(2-adamantyl)-2-methyl-3-aminopropanoate, were prepared in the course of the synthesis as intermediates. The anionic polymerization of lactam VI gave a polymer which was characterized by intrinsic viscosity, solubility, melting temperature and its IR and 1H NMR spectra. Compared with 3-butyl-3-methyl-2-azetidinone, lactam VI polymerizes much more slowly.

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18

Fujita, Tetsuro, Ryoji Hirose, Masahiko Yoneta, et al. "Potent Immunosuppressants, 2-Alkyl-2-aminopropane-1,3-diols1." Journal of Medicinal Chemistry 39, no. 22 (1996): 4451–59. http://dx.doi.org/10.1021/jm960391l.

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19

Knabe, Joachim, and Wolfgang Buchheit. "Chirale 3-Aminopropanole, 1. Mitt. Synthese der Racemate und der Enantiomere." Archiv der Pharmazie 318, no. 7 (1985): 593–600. http://dx.doi.org/10.1002/ardp.19853180705.

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20

Ike, Yuji, and Seiji Kojima. "Brillouin scattering study of liquid–glass transitions of aminopropanols." Journal of Molecular Structure 744-747 (June 2005): 521–24. http://dx.doi.org/10.1016/j.molstruc.2004.10.120.

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21

Perigaud, A., and Y. F. Nicolau. "Growth of methyl 2-(2,4-dinitrophenyl)aminopropanoate single crystals." Journal of Crystal Growth 79, no. 1-3 (1986): 752–57. http://dx.doi.org/10.1016/0022-0248(86)90550-6.

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22

Popa, Flavia, Pedro Lameiras, Eric Henon, et al. "Amino-s-triazines — Synthesis and stereochemistry of restricted rotational phenomena — First use of a C-2-substituted serinol in tandem with masked 4-piperidone for selective amination of cyanuric chloride." Canadian Journal of Chemistry 89, no. 10 (2011): 1207–21. http://dx.doi.org/10.1139/v11-075.

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Starting from 4-piperidone monohydrate hydrochloride (or the hydrochloride of its ethylene ketal) alone, otherwise in tandem with a C-2-substituted 2-aminopropane-1,3-diol (“serinol”) as amino-nucleophiles in reaction with cyanuric chloride, the synthesis of novel N-substituted amino-s-triazines is reported. The stereochemistry of rotational phenomena occurring about the newly created C(s-triazine)–N< (exocyclic) partial double bonds in the title compounds, seen as new dendritic building blocks, is discussed.

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23

Persson, L., A. R. Khomutov, and R. M. Khomutov. "Feedback regulation of S-adenosylmethionine decarboxylase synthesis." Biochemical Journal 257, no. 3 (1989): 929–31. http://dx.doi.org/10.1042/bj2570929.

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Treatment of Ehrlich ascites-tumour cells with 1-amino-oxy-3-aminopropane (AOAP), a potent inhibitor of ornithine decarboxylase, resulted in a marked decrease in cellular contents of putrescine and spermidine, concomitant with an arrest of cell growth. The activity of S-adenosylmethionine decarboxylase (AdoMetDC) was greatly increased in cells treated with AOAP. This increase in AdoMetDC activity was shown to be, at least partly, caused by enhanced synthesis of the enzyme, which most likely was induced by the change in cellular polyamine content.

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24

De Loos, Theodoor W., Hendrikus R. Tijsseling, and Jakob De Swaan Arons. "Vapor-liquid equilibria of the system ethane + 2-aminopropane." Journal of Chemical & Engineering Data 32, no. 3 (1987): 374–77. http://dx.doi.org/10.1021/je00049a027.

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25

Beşli, Serap. "Isomeric spiro and ansa macrocyclic derivatives of spiro-aminopropanoxy-cyclotriphosphazene." Inorganic Chemistry Communications 8, no. 5 (2005): 449–52. http://dx.doi.org/10.1016/j.inoche.2005.02.009.

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26

Gajewski, Mariusz, and Leszek Czuchajowski. "Phosphorus (V) porphyrin diaxially substituted with Leu-enkephalin." Open Chemistry 2, no. 3 (2004): 446–55. http://dx.doi.org/10.2478/bf02476200.

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AbstractSynthesis of the first phosphorus (V) porphyrin-peptide conjugate was successfully accomplished. A biologically active peptide, leucine enkephalin, was constructed on the phosphorus atom of the 5,10,15,20-meso-tetraphenylporphinato dichlorophosphorus (V) chloride. The method involved solution phase peptide synthesis. The first C-terminal amino acid in the sequence of the peptide was axially attached to the porphyrin through a linker, 3-aminopropanol, and the remainder of leucine enkephalin was synthesized by subsequent additions of amino acids. Leucine enkephalin-P(V) porphyrin conjuga

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27

Kelterer, Anne-Marie, Michaela Flock, and Michael Ramek. "Ab initio SCF investigation of 3-aminopropanol and 3-aminopropanal." Journal of Molecular Structure: THEOCHEM 276 (December 1992): 35–59. http://dx.doi.org/10.1016/0166-1280(92)80022-e.

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28

Ramek, Michael, Michaela Flock, Anne-Marie Kelterer та Vincent K. W. Cheng. "Intramolecular interactions in β-alanine, 3-aminopropanal and 3-aminopropanol". Journal of Molecular Structure: THEOCHEM 276 (грудень 1992): 61–81. http://dx.doi.org/10.1016/0166-1280(92)80023-f.

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29

Blum, Helmut. "Synthese, Eigenschaften und Struktur neuer 1,1-Diphosphonsäuren / Synthesis, Properties and Structure of New 1,1-Diphosphonic Acids." Zeitschrift für Naturforschung B 43, no. 1 (1988): 75–81. http://dx.doi.org/10.1515/znb-1988-0114.

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Abstract The synthesis of 3-tert-alkyl-3-oxo-1-arninopropane-1,1-diphosphonic acids and of 3-tert-alkyl-3-oxo-prop-1-ene-1,1-diphosphonic acids as two new groups of metal complexing agents and their chemical properties are described. Evidence is given for their suggested structures. In addition, the first known example of a diphosphonic acid with a cyano group attached to the geminal carbon atom was prepared from 3-oxo-1-aminoalkane-1,1-diphosphonic acids and 3-terr-alkyl-3-oxo-1-hydroxypropane-1,1-diphosphonic acids from 3-oxo-1-aminopropane-1,1-diphosphonic acids.

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30

Zagppey, Herman, Roel H. Fokkens, Steen Ingemann, Nico M. M. Nibbering, and Helena Florencio. "Site of gas-phase methylation of l-phenyl-2-aminopropane." Organic Mass Spectrometry 26, no. 6 (1991): 587–94. http://dx.doi.org/10.1002/oms.1210260610.

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31

Glennon, Richard A., Mamoun Yousif, and Graham Patrick. "Stimulus properties of 1-(3,4-methylenedioxyphenyl)-2-aminopropane (MDA) analogs." Pharmacology Biochemistry and Behavior 29, no. 3 (1988): 443–49. http://dx.doi.org/10.1016/0091-3057(88)90001-9.

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32

Glennon, Richard A., Richard Young, Małgorzata Dukat, Jean Chang-Fong, and Mohamed El-Zahabi. "N-Methyl-1-(4-methoxyphenyl)-2-aminopropane (PMMA) and N-Methyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane (MDMA) produce non-identical discriminative stimuli in rats." Pharmacology Biochemistry and Behavior 86, no. 3 (2007): 477–84. http://dx.doi.org/10.1016/j.pbb.2007.01.007.

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33

Czerkas, S., A. Burczyk, J. JadŻyn, and M. Stockhausen. "Viscosity of Some Propanols and Aminopropanols in Mixtures with 1,4-Dioxane." Physics and Chemistry of Liquids 37, no. 1 (1998): 1–7. http://dx.doi.org/10.1080/00319109808032795.

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34

Arutyunyan, N. S., L. A. Akopyan, N. A. Apoyan, A. E. Tumadzhyan, and S. A. Vartanyan. "Synthesis and study of the antiinflammatory properties of tetrahydropyran-substituted ?-aminopropanols." Pharmaceutical Chemistry Journal 23, no. 2 (1989): 144–46. http://dx.doi.org/10.1007/bf00764464.

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35

Bredikhina, Z. A., A. V. Kurenkov, and A. A. Bredikhin. "Nonracemic Dimethylphenyl Glycerol Ethers in the Synthesis of Physiologically Active Aminopropanols." Russian Journal of Organic Chemistry 55, no. 6 (2019): 837–44. http://dx.doi.org/10.1134/s1070428019060149.

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36

Arm, Kenji, Shohei Tamura, Tatsuya Masumizu, Ken-Ichi Kawai, Shoichi Nakajima, and Akira Ueda. "A novel electrochemical method for benzoylation of aminoalcohols with methyl benzoates at room temperature." Canadian Journal of Chemistry 68, no. 6 (1990): 903–7. http://dx.doi.org/10.1139/v90-142.

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A novel electrochemical method of benzoylating aminoalcohols 2 by use of methyl benzoates 1 at room temperature was developed. 2-Aminoethanols 2 (n = 0, R3 = H) and 3-aminopropanols 2 (n = 1, R3 = H) gave the corresponding benzamides 4, as a result of electrochemical transesterification followed by O,N-actyl migration. In contrast, o- and m-aminobenzylalcohols (7a and 7b) and trans-4-(aminomethyl)cyclohexanemethanol (8a) afforded the corresponding benzoic esters, since their acyl migration is hindered. A local anesthetic, procaine, was prepared by using this electrochemical reaction. A mechani

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37

Foster, B. C., D. L. Wilson, T. Marwood, J. C. Ethier, and J. Zamecnik. "Microbial transformation of 3,4-methylenedioxy-N-methylamphetamine and 3,4-methylenedioxyamphetamine." Canadian Journal of Microbiology 42, no. 8 (1996): 851–54. http://dx.doi.org/10.1139/m96-107.

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The biotransformation of 3,4-methylenedioxy-N-methylarnphetamine (MDMA) and 3,4-methylenedioxyamphetamine (MDA) was examined in the fungus Cunninghamella echinulata. In addition to the reported mammalian metabolites (MDA, 3,4-methylenedioxybenzyl methyl ketoxime, 3,4-methylenedioxybenzyl methyl ketone) and the parent substrate, there were six novel metabolites detected. N-Acetyl-3,4-methylenedioxyamphetamine (NAcMDA) was unequivocally identified and three unidentified metabolites related to NAcMDA were also detected. N-Acetyl-3,4-methylenedioxy-1-phenyl-1-hydroxy-2-aminopropane was tentatively

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38

Jílek, Jiří, Jiří Urban, Vojtěch Kmoníček, et al. "Potential anticonvulsants: 3-Chlorobenzophenone derivatives." Collection of Czechoslovak Chemical Communications 54, no. 8 (1989): 2248–60. http://dx.doi.org/10.1135/cccc19892248.

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Reactions of 2-(2-iodoacetamido)-5-chlorobenzophenone with 2-amino-2-phenylethanol, 2-amino-1-phenylethanol, 3-amino-2-phenylpropanol, D-(+)-norpseudoephedrine, and 2-aminopropane-2-carbonitrile gave the 2-substituted N-(2-benzoyl-4-chlorophenyl)acetamides X-XIV. 2,3'-Dichlorobenzhydrol (XVI) and 2,3'-dichlorobenzhydryl chloride (XIX) were transformed to the ethers XVII and XVIII and to the amines XXI-XXIV. Compound XVI was oxidized to the ketone XXV which was transformed via the oxime XXVI to compound XXVII. The basic products were converted to salts which were pharmacologically tested. Compo

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39

Chiarino, D., F. Ferrario, M. Napoletano, and A. Sala. "Synthesis of new [[(3-substituted-5-isoxazolyl)-alkyliden]iminooxy]aminopropanol derivatives." Journal of Heterocyclic Chemistry 25, no. 5 (1988): 1359–62. http://dx.doi.org/10.1002/jhet.5570250516.

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40

Giang, Le Nhat Thuy, Doan Duy Tien, Dang Thi Tuyet Anh, et al. "Synthesis and Cytotoxic Evaluation of Artemisinin Derivatives Containing an Aminopropanol Group." Natural Product Communications 13, no. 8 (2018): 1934578X1801300. http://dx.doi.org/10.1177/1934578x1801300801.

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Series of novel artemisinin derivatives were designed and synthesized in which the amino propanol group was bonded to the artemisinin nucleus through C-C linkage. Ten new compounds were thus successfully prepared and evaluated as cytotoxic agents, revealing an interesting anticancer activity in KB and HepG2 cancer cell lines.

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41

Kelterer, Anne-Marie, and Michael Ramek. "Intramolecular hydrogen bonding in 2-aminoethanol, 3-aminopropanol and 4-aminobutanol." Journal of Molecular Structure: THEOCHEM 232 (July 1991): 189–201. http://dx.doi.org/10.1016/0166-1280(91)85254-5.

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42

Glozman, O. M., �. K. Orlova, �. S. Agavelyan, et al. "Synthesis and pharmacological activity of 1-phenoxy-3-aminopropanol-2-derivatives." Pharmaceutical Chemistry Journal 21, no. 3 (1987): 197–200. http://dx.doi.org/10.1007/bf01146183.

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43

Kuo, Mei-Tsan, Jie-Ning Yang, Jim Jr-Min Lin, and Kaito Takahashi. "Substituent Effect in the Reactions between Criegee Intermediates and 3-Aminopropanol." Journal of Physical Chemistry A 125, no. 30 (2021): 6580–90. http://dx.doi.org/10.1021/acs.jpca.1c03737.

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44

Hamana, Koel, Masaru Niitsu, and Keijiro Samejima. "Further polyamine analyses of leguminous seeds and seedlings: the occurrence of novel linear, tertiary branched and quaternary branched pentaamines." Canadian Journal of Botany 74, no. 11 (1996): 1766–72. http://dx.doi.org/10.1139/b96-213.

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Polyamines of the seeds, seedlings, and some other tissues of 15 leguminous plants were analyzed by high performance liquid chromatography and gas chromatography. A novel tertiary branched pentaamine, N5-aminobutylhomospermine, was detected in the seed of Vicia villosa and another novel quaternary branched pentaamine, N4-bis(aminopropyl)spermidine, in the seed of Crotalaria spectabilis. Norspermine and a novel linear pentaamine, caldopentamine, were found in the seed of Gleditschia japonica. Other unusual polyamines such as norspermidine, homospermidine, thermospermine, N4-methylthermospermine

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45

Saloutin, Victor I., Marina V. Goryaeva, Svetlana O. Kushch, et al. "Competitive ways for three-component cyclization of polyfluoroalkyl-3-oxo esters, methyl ketones and amino alcohols." Pure and Applied Chemistry 92, no. 8 (2020): 1265–75. http://dx.doi.org/10.1515/pac-2019-1216.

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AbstractThe competitive routes were found for three-component cyclization of polyfluoroalkyl-3-oxo esters, methyl ketones with 3-amino alcohols. It was shown that the reactions with 3-aminopropanol in 1,4-dioxane predominantly lead to hexahydropyrido[2,1-b][1,3]oxazin-6-ones, and in ethanol to 3-hydroxypropylaminocyclohexenones. In contrast, cyclizations with 2-aminoethanol and its analogues, regardless of the reaction conditions, yield hexahydrooxazolo[3,2-a]pyridin-5-ones as the main products. The trans- and cis-diastereomeric structure of heterocycles was established using X-ray and 1H, 19F

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46

Tengler, Jan, Iva Kapustíková, Ondřej Stropnický, et al. "Synthesis of new (arylcarbonyloxy)aminopropanol derivatives and the determination of their physico-chemical properties." Open Chemistry 11, no. 11 (2013): 1757–67. http://dx.doi.org/10.2478/s11532-013-0302-8.

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AbstractEight hydrochlorides of 3-{2-[(2/4-fluorophenoxy)-ethylamino]}-2-hydroxypropyl-4-alkoxybenzoates and four hydrochlorides of 3-tert-butylamino-2-hydroxypropyl-4-butoxybenzoates were prepared as potential antagonists of the β1-adrenergic receptor (beta-blockers). A multistep synthesis of these compounds is described as well as their detailed analytical characterization. The pharmacokinetic properties of these weak base compounds are significantly influenced by their acid-base dissociation constant, pK a. The knowledge of this value is crucial for new drug development. This paper is aimed

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47

Shaju, K. S., K. Joby Thomas, Vinod P. Raphael, and Aby Paul. "Synergistic Effect of KI on Corrosion Inhibition of Mild Steel by Polynuclear Schiff Base in Sulphuric Acid." ISRN Corrosion 2012 (December 5, 2012): 1–8. http://dx.doi.org/10.5402/2012/425878.

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Synergistic effect of KI on the corrosion inhibition efficiency of polynuclear Schiff base, anthracene-9(10H)-one-3-aminopropanoic acid (A9O3AP), on mild steel (MS) in 0.5 M sulphuric acid solution has been investigated using weight loss measurements, electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization studies. The results show that inhibition efficiencies on MS increase with increase in concentration of the inhibitor and enhancement in inhibition efficiency was observed on addition of potassium iodide due to synergism. The adsorptions, of inhibitor and inhibitor + K

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48

Luberda-Durnaś, K., B. Gaweł, M. Łoś, and W. Łasocha. "Synthesis and characterization of inorganic-organic ZnS(aminopropane)n composite materials." Crystal Research and Technology 46, no. 12 (2011): 1283–90. http://dx.doi.org/10.1002/crat.201100380.

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49

Zelenin, K. N., and I. V. Ukraintsev. "Ring-chain tautomerism in the hydropyrimidine -1-benzylideneamino-3-aminopropane systems." Chemistry of Heterocyclic Compounds 32, no. 8 (1996): 985. http://dx.doi.org/10.1007/bf01176981.

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Felix, Hansruedi, and Jost Harr. "Influence of Inhibitors of Polyamine Biosynthesis on Polyamine Levels and Growth of Plants." Zeitschrift für Naturforschung C 44, no. 1-2 (1989): 55–58. http://dx.doi.org/10.1515/znc-1989-1-210.

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Abstract:

Abstract Inhibitors of enzymes involved in polyamine biosynthesis which stop the growth of bacteria, fungi and animal cell systems were analyzed for their potential to interfere with plant cell systems. Several compounds were found to be potent inhibitors of plant enzymes, namely the decarboxylases of ornithine, arginine and S-adenosylmethionine as well as the aminopropyltransferase. Application of enzyme inhibitors (α-difluoromethylornithine. l-aminooxy-3-aminopropane, a-difluoromethylarginine, methylglyoxal bis(guanyl-hydrazone), cyclohexylamine) or combinations of these on whole plant syste

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