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Relevant bibliographies by topics / Amines

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Academic literature on the topic 'Amines'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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Journal articles on the topic "Amines"

1

Budynina, Ekaterina, Konstantin Ivanov, Ivan Sorokin, and Mikhail Melnikov. "Ring Opening of Donor–Acceptor Cyclopropanes with N-Nucleophiles." Synthesis 49, no. 14 (2017): 3035–68. http://dx.doi.org/10.1055/s-0036-1589021.

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Ring opening of donor–acceptor cyclopropanes with various N-nucleophiles provides a simple approach to 1,3-functionalized compounds that are useful building blocks in organic synthesis, especially in assembling various N-heterocycles, including natural products. In this review, ring-opening reactions of donor–acceptor cyclopropanes with amines, amides, hydrazines, N-heterocycles, nitriles, and the azide ion are summarized.1 Introduction2 Ring Opening with Amines3 Ring Opening with Amines Accompanied by Secondary Processes Involving the N-Center3.1 Reactions of Cyclopropane-1,1-diesters with Pr

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Yao, Lei, Ming-Yi Wang, Xin-Ke Wang, et al. "Detection of atmospheric gaseous amines and amides by a high-resolution time-of-flight chemical ionization mass spectrometer with protonated ethanol reagent ions." Atmospheric Chemistry and Physics 16, no. 22 (2016): 14527–43. http://dx.doi.org/10.5194/acp-16-14527-2016.

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Abstract. Amines and amides are important atmospheric organic-nitrogen compounds but high time resolution, highly sensitive, and simultaneous ambient measurements of these species are rather sparse. Here, we present the development of a high-resolution time-of-flight chemical ionization mass spectrometer (HR-ToF-CIMS) method, utilizing protonated ethanol as reagent ions to simultaneously detect atmospheric gaseous amines (C1 to C6) and amides (C1 to C6). This method possesses sensitivities of 5.6–19.4 Hz pptv−1 for amines and 3.8–38.0 Hz pptv−1 for amides under total reagent ion signals of ∼ 0

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Qu, Jing, Shishan Yu, Wenzhao Tang, Yunbao Liu, Yue Liu, and Jing Liu. "Progress on Cassaine-Type Diterpenoid Ester Amines and Amides (Erythrophleum Alkaloids)." Natural Product Communications 1, no. 10 (2006): 1934578X0600101. http://dx.doi.org/10.1177/1934578x0600101005.

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The structures, spectral characteristics, and bioactivities of 39 natural cassaine-type diterpenoid ester amines and amides (Erythrophleum alkaloids) and 31 synthetic analogues are reviewed. Cassaine-type diterpenoid ester amines and amides, the so called Erythrophleum alkaloids, have the skeleton of cassane-type diterpenoids with a N-containing side chain, and are classified into two groups, ester amines and amides. Cassaine-type diterpenoid ester amines and amides show remarkable inotropic action on the heart, inhibition of Na+/K+-ATPase, cytotoxities, and other major bioactivities. Structur

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Barham, Joshua P., та Jaspreet Kaur. "Site-Selective C(sp3)–H Functionalizations Mediated by Hydrogen Atom Transfer Reactions via α-Amino/α-Amido Radicals". Synthesis 54, № 06 (2021): 1461–77. http://dx.doi.org/10.1055/a-1677-6619.

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AbstractAmines and amides, as N-containing compounds, are ubiquitous in pharmaceutically-active scaffolds, natural products, agrochemicals, and peptides. Amides in nature bear a key responsibility for imparting three-dimensional structure, such as in proteins. Structural modifications to amines and amides, especially at their positions α to N, bring about profound changes in biological activity oftentimes leading to more desirable pharmacological profiles of small drug molecules. A number of recent developments in synthetic methodology for the functionalizations of amines and amides omit the n

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Xu, Qing, Huamei Xie, Er-Lei Zhang, et al. "Selective catalytic Hofmann N-alkylation of poor nucleophilic amines and amides with catalytic amounts of alkyl halides." Green Chemistry 18, no. 14 (2016): 3940–44. http://dx.doi.org/10.1039/c6gc00938g.

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A selective Hofmann N-alkylation reaction of amines/amides catalytic in alkyl halides is achieved by using alcohols as the alkylating reagents, affording mono- or di-alkylated amines/amides in high selectivities.

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North, Michael. "Amines and amides." Journal of the Chemical Society, Perkin Transactions 1, no. 16 (1999): 2209–29. http://dx.doi.org/10.1039/a903369f.

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North, Michael. "Amines and amides." Contemporary Organic Synthesis 1, no. 6 (1994): 475. http://dx.doi.org/10.1039/co9940100475.

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North, Michael. "Amines and amides." Contemporary Organic Synthesis 2, no. 4 (1995): 269. http://dx.doi.org/10.1039/co9950200269.

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North, Michael. "Amines and amides." Contemporary Organic Synthesis 3, no. 4 (1996): 323. http://dx.doi.org/10.1039/co9960300323.

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North, Michael. "Amines and amides." Contemporary Organic Synthesis 4, no. 4 (1997): 326. http://dx.doi.org/10.1039/co9970400326.

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Dissertations / Theses on the topic "Amines"

1

Sandford, Graham. "Some amine hydrofluorides and amines in organofluorine chemistry." Thesis, Durham University, 1991. http://etheses.dur.ac.uk/6209/.

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Abrahamson, Michael J. "Development of an amine dehydrogenase." Diss., Georgia Institute of Technology, 2012. http://hdl.handle.net/1853/50138.

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Biocatalysts are increasingly prevalent in the large-scale synthesis of enantiomerically pure compounds. However, many sought-after reactions lack a suitable enzymatic production route. This work describes the development of a novel amine dehydrogenase through the application of directed evolution altering the substrate specificity of an existing leucine dehydrogenase scaffold. Eleven rounds of directed evolution completely altered the enzyme’s specificity and successfully created amination activity. The resulting amine dehydrogenase asymmetrically catalyzes methyl isobutyl ketone and free amm

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Kargina, Irina. "Topochemical reactions of amines and amides with titanium and vanadium oxychlorides." Thesis, University of Ottawa (Canada), 1995. http://hdl.handle.net/10393/10109.

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The intercalation of primary, secondary, tertiary, and aromatic amines into layered TiOCl have been investigated by a variety of methods. The intercalation reaction does not appear to be a redox process. A key step for intercalation of amines into host TiOCl is proposed to be a coordination via nitrogen lone electron pair to Ti$\sp{3+}$ metal centres. Subsequent substitution of the interlayer chloride ions of TiOCl by the amine molecules is strongly dependent on the properties of the organic compounds and their ability to form ammonium salts. Based on X-ray diffraction, fluorescence, elemental

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Ghislieri, Diego. "Application of engineered amine oxidases for the synthesis of chiral amines." Thesis, University of Manchester, 2013. https://www.research.manchester.ac.uk/portal/en/theses/application-of-engineered-amine-oxidases-for-the-synthesis-of-chiral-amines(de93d851-97f8-4422-8dc4-0f7402488021).html.

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The development of cost-effective and sustainable catalytic methods for the production of enantiomerically pure chiral amines is a key challenge facing the pharmaceutical and fine chemical industries. There is an increasing demand for broadly applicable synthetic methods which deliver the desired amine product in high yield and enantiomeric excess (e.e.). Previously we have described the development of variants of monoamine oxidase from Aspergillus niger (MAO-N) which are able to mediate the complete conversion of racemic amines to the corresponding enantiomerically pure products in a single s

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Rofouei, Mohammad Kazem. "The preparation, characterisation and reactivity of derivatives of a novel sterically demanding amido ligand." Thesis, University of Sussex, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361401.

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Johansen, Maren Teresa. "Degradation of Amines." Thesis, Norges teknisk-naturvitenskapelige universitet, Institutt for kjemi, 2013. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-23201.

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In view of the rising amounts of greenhouse gases in the atmosphere, preventing CO2 emissions has become increasingly important. The combustion of fossil fuels for energy production and transportation is a large contributor to the problem. One of the ways to reduce the amounts of CO2 being released from combustion is carbon capture and storage (CCS). Post-combustion is the capturing method which has been deemed the easiest to apply to existing power plants in a short period of time. Absorption of CO2 by MEA is the most common method used in post-combustion carbon capture, but there are still

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Heuson, Egon. "Recherche de nouvelles transaminases pour la synthèse d'amines chirales." Thesis, Clermont-Ferrand 2, 2015. http://www.theses.fr/2015CLF22659/document.

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Slatter, John Gregory. "Metabolism of tertiary arylaliphatic amines and formamides in rats." Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/29392.

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The metabolites of the basic tertiary arylaliphatic amine N,N,α-trimethyl-7-phenylbenzenepropanamine (RecipavrinR) from male Wistar rats were characterized by gas chromatography-mass spectrometry (GCMS). The work was undertaken in an attempt to determine the source of a novel metabolite, N-(1-methyl-3,3-diphenylpropyl) formamide. The formamide metabolite was isolated from the bile of recipavrin dosed rats only after hydrolysis with the enzyme β-glucuronidase, suggesting that it arose from a glucuronide conjugated precursor. Recipavrin was chosen for the study based on structural similarity to

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Li, Haiying. "A study on grafting poly(p-phenylene terephthalamide) with aliphatic amines and amides." Thesis, Georgia Institute of Technology, 1999. http://hdl.handle.net/1853/8594.

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Lizier, Thiago Mescoloto [UNESP]. "Análise de aminas aromáticas em amostras de interesse ambiental por cromatografia líquida de alta eficiência acoplada a detectores de arranjo de diodo, eletroquímico e espectrometria de massas: Thiago Mescoloto Lizier. -." Universidade Estadual Paulista (UNESP), 2014. http://hdl.handle.net/11449/110706.

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Made available in DSpace on 2014-11-10T11:09:59Z (GMT). No. of bitstreams: 0 Previous issue date: 2014-03-14Bitstream added on 2014-11-10T11:58:19Z : No. of bitstreams: 1 000775008_20160317.pdf: 583036 bytes, checksum: 0ca55e9eabbd518c68becabdeb61f788 (MD5) Bitstreams deleted on 2016-03-18T13:35:50Z: 000775008_20160317.pdf,. Added 1 bitstream(s) on 2016-03-18T13:36:33Z : No. of bitstreams: 1 000775008.pdf: 2574132 bytes, checksum: 055efec6156da665a55258df247b05c5 (MD5)<br>O presente trabalho investiga novos métodos analíticos para análise de aminas aromáticas selecionadas em virtude de suas

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Books on the topic "Amines"

1

G, Baumgartner William, ed. Amines. Freedonia Group, 1998.

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L, Hayes Teresa, Richardson Michael B, Friedman Rebecca L, and Freedonia Group, eds. Amines. Freedonia Group, 2000.

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Boulton, A. A., A. V. Juorio, and R. G. H. Downer, eds. Trace Amines. Humana Press, 1988. http://dx.doi.org/10.1007/978-1-4612-4602-2.

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4

Bruno, Mondovì, ed. Structure and functions of amine oxidases. CRC Press, 1985.

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Kagakkai, Nihon Bunseki. Aminosan, seitai amin bunseki. Maruzen Shuppan, 2012.

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Boulton, Alan A., Glen B. Baker, and Judith M. Baker. Amines and Their Metabolites. Humana Press, 1985. http://dx.doi.org/10.1385/0896030768.

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Li, Wei, and Xumu Zhang, eds. Stereoselective Formation of Amines. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53929-9.

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8

Saad, Bahruddin, and Rosanna Tofalo, eds. Biogenic Amines in Food. Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015813.

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A, Boulton A., Baker Glen B. 1947-, and Baker Judith M, eds. Amines and their metabolites. Humana Press, 1985.

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Follain, Nadege. Amines grafted cellulose materials. Nova Science Publishers, 2010.

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Book chapters on the topic "Amines"

1

Börnick, Hilmar, and Torsten C. Schmidt. "Amines." In Organic Pollutants in the Water Cycle. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/352760877x.ch8.

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Gooch, Jan W. "Amines." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_555.

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Tucker, William B. "Amines." In Organic Chemistry. CRC Press, 2024. http://dx.doi.org/10.1201/9781003479352-23.

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Sourkes, T. L. "Copper, Biogenic Amines, and Amine Oxidases." In Novartis Foundation Symposia. John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470720622.ch8.

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Yon, A. Marjorie, B. Jean-Daniel Marty, and C. Diana Ciuculescu-Pradines. "CHAPTER 6. Amines and Amine-boranes." In Reducing Agents in Colloidal Nanoparticle Synthesis. Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839163623-00130.

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Khan, JaVed I., Thomas J. Kennedy, and Donnell R. Christian. "Tertiary Amines." In Basic Principles of Forensic Chemistry. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-59745-437-7_14.

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Sahar, Amna, Ubaid ur Rahman, Muhammad Issa Khan, and Muhammad Azam Khan. "Heterocyclic Amines." In Food Safety. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-39253-0_5.

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Turiault, Marc, Caroline Cohen, Guy Griebel, et al. "Trace Amines." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_211.

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Tyrer, Peter J., Mark Slifstein, Joris C. Verster, et al. "Biogenic Amines." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_598.

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Tomlinson, Sara, Darrell D. Mousseau, Glen B. Baker, and Ashley D. Radomski. "Trace Amines." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-36172-2_211.

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Conference papers on the topic "Amines"

1

Tomoe, Y., M. Shimizu, and H. Kaneta. "Active Dissolution and Natural Passivation of Carbon Steel in Carbon Dioxide-Loaded Alkanolamine Solutions." In CORROSION 1996. NACE International, 1996. https://doi.org/10.5006/c1996-96395.

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Abstract Corrosion rates of carbon steel specimens were measured in carbon dioxide(CO2)-loaded alkanolamine(amine) solutions by weight-loss tests and by the polarization resistance method. In dilute amine solutions, lower than 10[[illegible]] M, corrosion rates were controlled by the formation of protective FeCO3 scale as in hot, CO2 -H2O environments. Tested amines inhibited CO2 induced corrosion in the concentration range between 10-2 and 2M. In concentrated amine solutions, higher than 3M, primary and tertiary amines showed markedly different effects on carbon steel corrosion. The corrosion

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Nagu, Muthukumar, Saroj K. Panda, and Nayef M. Alanazi. "Organic Amine Partitioning at Simulated Refinery Overhead Condition." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-13225.

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Abstract Organic amines, a neutralizer, are preferentially used over ammonia to minimize the amine hydrochloride induced corrosion in refinery overhead systems. The partition of active ingredients of the neutralizers to the hydrocarbon phase reduces the efficiency of neutralizing amines as the maximum amount of amines are required to be in the aqueous phase to deal with hydrochloric acid present in the system. Moreover, the partitioning of amines to the hydrocarbon phase can form corresponding amine chloride salts leading to the under deposit corrosion in the refinery units. In the present inv

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Jayaweera, P., S. Hettiarachchi, and P. J. Millett. "Decomposition of Some Amines and Amino Acids in Steam Generator Environments." In CORROSION 1994. NACE International, 1994. https://doi.org/10.5006/c1994-94167.

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Abstract Hydrothermal decomposition rate constants and high temperature pH values of some selected high-molecular weight amines and amino acids were measured under simulated steam generator conditions. These amines and amino acids were evaluated as potential crevice buffering agents for steam generator applications in pressurized water reactors. The study showed that, although the high molecular weight amines undergo hydrothermal decomposition, they have a better buffer capacity than their low molecular weight counterparts at 290°C. The amines provide effective crevice buffering by increasing

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Pinappu, Sai Reddy, Kwadwo Sarpong, Corina Sandu, and Zhenning Gu. "Fast On-Site Quantification and Monitoring of Monoethanolamine in Crude Oils Using Field Asymmetric Ion Mobility Spectrometry." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05630.

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Abstract Triazine-based hydrogen sulfide (H2S) scavengers are the most commonly used additives in the oil and gas industry. One of the reaction products of the scavenging process is an organic amine. The organic amine by-product, together with amines in slop oil and the desalter wash water, are collectively referred to as “tramp amines.” The most-common tramp amines from the H2S scavenging process are mono-ethanolamine (MEA) and methylamine (MA). These tramp amines have the potential to react with hydrochloric acid (HCl) to form corrosive amine hydrochloride salts in the crude atmospheric dist

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Lack, Joel, and Bradley Harrell. "Reducing Salt Corrosion Rates with Stronger Base Amines." In CORROSION 2013. NACE International, 2013. https://doi.org/10.5006/c2013-02037.

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Abstract When processing discounted crude oils, one of the primary challenges refiners face is under-salt corrosion in crude unit distillation overhead systems. The combination of higher overhead chloride levels and the presence of amine contaminants in discounted crudes can greatly increase the risk of salt formation. For those overhead systems where amine salt corrosion cannot be mitigated by conventional methods, the application of non-traditional neutralizing amines can provide benefit. In particular, under-salt corrosion rates produced by stronger base amines are significantly less than t

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Alratoee, Abdullah M., Ibrahim A. Albrahim, Ricardo S. Costa, and Sayee Raghunathan. "Combatting Corrosion in Gas Sweetening Processes: Insight from Amine Treatment Case Studies." In CONFERENCE 2024. AMPP, 2024. https://doi.org/10.5006/c2024-21052.

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Abstract Amine solutions have been widely used to remove acid gases at gas treatment units found in gas plants, refineries and other facilities. Corrosion is always a challenge for these units, particularly for carbon steel equipment or piping that are processing hot amines. Amines are noncorrosive by nature. However, once acid gases are dissolved in amines, they act as strong electrolytes, which significantly increase the susceptibly of carbon steel components to corrode. Temperature, acid gas loading, velocity, and degradation products are the primary factors that influence amine corrosion.

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Hepp, Doug, Gary Wein, and William Bornak. "User Experience: Control of Copper Corrosion in a Steel Mill Surface Condenser with Amine Neutralization." In CORROSION 1986. NACE International, 1986. https://doi.org/10.5006/c1986-86381.

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Abstract A complicated copper corrosion problem in a turbine surface condenser was controlled with amine neutralization. To more closely control the costs of the treatment, a system-specific computer program was developed, factoring in amine distribution ratio, neutralizing capacity, feedwater alkalinity, etc. Analysis of 2-year performance/treatment data corroborated the predictions of the computer program. The treatment was further optimized by feeding a test mixture of amines to the system. After equilibrium was reached, samples from key locations were analyzed for individual amines, pH val

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Duggan, G. G., and R. G. Rechtien. "Application of Ionic Equilibria Process Simulation for Atmospheric Distillation Overhead Systems." In CORROSION 1998. NACE International, 1998. https://doi.org/10.5006/c1998-98586.

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Abstract The use of organic neutralizing amines in distillation overhead systems is a common refinery corrosion control practice. Two problems are often encountered in these amine applications: underdeposit corrosion attack resulting from the deposition of amine-hydrochloride salts and aggressive acid corrosion in the vicinity of the aqueous dewpoint. Often it is the misapplication of neutralizers that creates these problems. To address these neutralizer concerns, the fundamental data required to accurately predict the behavior of these amines and their hydrochloride salts has been developed.

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Alghamdi, Talal M. "On-Site Sampling and Determination of Aliphatic Amines in Industrial Waste Water Using Solid Phase Microextraction (SPME)." In CORROSION 2014. NACE International, 2014. https://doi.org/10.5006/c2014-3935.

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Abstract Amine-based corrosion inhibitors are added to the crude oil streams to protect the pipelines from corrosive attacks by oxygen. Amine residuals should be monitored in the system and this is classically done by liquid-liquid extraction (LLE) of amines followed by colorimetric determination using spectrophotometry. Solid phase microextraction (SPME), a novel extraction technique, was used as a sample preparation technique to isolate the amines from the complex sample matrix and gas chromatography (GC) system was used for separation and quantification of amines. A flow-through system was

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Lack, Joel E. "An in-Depth Look at Amine Behavior in Crude Units Using Electrolyte-Based Simulation." In CORROSION 2005. NACE International, 2005. https://doi.org/10.5006/c2005-05570.

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Abstract The use of organic amines to neutralize crude tower overhead waters is a common corrosion control practice in refineries. However, their presence in the system can lead to corrosion problems caused by reaction with hydrogen chloride to form corrosive salts. Use of overhead waters as a desalter wash source can aggravate the problem by building up the concentration of amine in the preheat systems, tower and associated product and pumparound systems. Electrolyte-based simulation has provided valuable insight into the vapor-liquid-aqueous partitioning behavior of commonly encountered amin

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Reports on the topic "Amines"

1

Selig, W. Determination of equivalent weight of amines. Office of Scientific and Technical Information (OSTI), 1987. http://dx.doi.org/10.2172/6881693.

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Thomson, J. S., J. B. Green, T. B. McWilliams, and S. K. T. Yu. GC/MS determination of amines following exhaustive trifluoroacetylation. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10180988.

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Hameka, Hendrik F., George R. Famini, James O. Jensen, and E. I. Newhouse. Computations of Vibrational Infrared Frequencies of Selected Amines. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada218840.

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Mossine, Valerie V. Multivalent Lactulose-amines as Inhibitors of Prostate Cancer Metastasis. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada406249.

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Hameka, H. F., G. R. Famini, J. O. Jensen, and J. L. Jensen. Theoretical Prediction of Vibrational Infrared Frequencies of Tertiary Amines. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada232880.

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Overly, Joyce, and Deanne Snavely. Vibrational Overtone Spectroscopy of Cyclic Amines: Pyridine and Related Compounds. Defense Technical Information Center, 1993. http://dx.doi.org/10.21236/ada265524.

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Adams, R. The transformation of organic amines by transition metal cluster compounds. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/7108222.

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Frechet, Jean M., and James F. Cameron. Photogenerated Amines and Diamines: Novel Curing Systems for Thin Film Coatings. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada235568.

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Adams, R. D. The transformation of organic amines by transition metal cluster compounds: Progress report. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10105409.

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Rosen, R. K. Reaction of Tris(cyclopentadienyl)uranium compounds with amines, azides, and related ligands. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/7257519.

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