Academic literature on the topic 'Amines'
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Journal articles on the topic "Amines"
Budynina, Ekaterina, Konstantin Ivanov, Ivan Sorokin, and Mikhail Melnikov. "Ring Opening of Donor–Acceptor Cyclopropanes with N-Nucleophiles." Synthesis 49, no. 14 (May 18, 2017): 3035–68. http://dx.doi.org/10.1055/s-0036-1589021.
Full textBarham, Joshua P., and Jaspreet Kaur. "Site-Selective C(sp3)–H Functionalizations Mediated by Hydrogen Atom Transfer Reactions via α-Amino/α-Amido Radicals." Synthesis 54, no. 06 (October 25, 2021): 1461–77. http://dx.doi.org/10.1055/a-1677-6619.
Full textManthey, MK, SG Pyne, and RJW Truscott. "Addition of Aliphatic and Aromatic Amines to Catechol in Aqueous Solution Under Oxidizing Conditions." Australian Journal of Chemistry 42, no. 3 (1989): 365. http://dx.doi.org/10.1071/ch9890365.
Full textOs, Van M., Van A. M. Vuuren, and S. F. Spoelstra. "Mechanisms of adaptation in sheep to overcome silage intake depression induced by biogenic amines." British Journal of Nutrition 77, no. 3 (March 1997): 399–415. http://dx.doi.org/10.1079/bjn19970041.
Full textSaha, Sayantani, and Moris S. Eisen. "Mild catalytic deoxygenation of amides promoted by thorium metallocene." Dalton Transactions 49, no. 36 (2020): 12835–41. http://dx.doi.org/10.1039/d0dt02770g.
Full textYedage, Subhash L., Denvert S. D'silva, and Bhalchandra M. Bhanage. "MnO2 catalyzed formylation of amines and transamidation of amides under solvent-free conditions." RSC Advances 5, no. 98 (2015): 80441–49. http://dx.doi.org/10.1039/c5ra13094h.
Full textLeggio, A., E. L. Belsito, G. De Luca, M. L. Di Gioia, V. Leotta, E. Romio, C. Siciliano, and A. Liguori. "One-pot synthesis of amides from carboxylic acids activated using thionyl chloride." RSC Advances 6, no. 41 (2016): 34468–75. http://dx.doi.org/10.1039/c5ra24527c.
Full textZhang, Qiao, Xiao-Tao Lin, Norihisa Fukaya, Tadahiro Fujitani, Kazuhiko Sato, and Jun-Chul Choi. "Selective N-formylation/N-methylation of amines and N-formylation of amides and carbamates with carbon dioxide and hydrosilanes: promotion of the basic counter anions of the zinc catalyst." Green Chemistry 22, no. 23 (2020): 8414–22. http://dx.doi.org/10.1039/d0gc02890h.
Full textCharron, Carlie L., Jade M. Cottam Jones, and Craig A. Hutton. "Are Aminomethyl Thioesters Viable Intermediates in Native Chemical Ligation Type Amide Bond Forming Reactions?" Australian Journal of Chemistry 71, no. 9 (2018): 697. http://dx.doi.org/10.1071/ch18198.
Full textYao, Lei, Ming-Yi Wang, Xin-Ke Wang, Yi-Jun Liu, Hang-Fei Chen, Jun Zheng, Wei Nie, 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 (November 23, 2016): 14527–43. http://dx.doi.org/10.5194/acp-16-14527-2016.
Full textDissertations / Theses on the topic "Amines"
Sandford, Graham. "Some amine hydrofluorides and amines in organofluorine chemistry." Thesis, Durham University, 1991. http://etheses.dur.ac.uk/6209/.
Full textKargina, Irina. "Topochemical reactions of amines and amides with titanium and vanadium oxychlorides." Thesis, University of Ottawa (Canada), 1995. http://hdl.handle.net/10393/10109.
Full textAbrahamson, Michael J. "Development of an amine dehydrogenase." Diss., Georgia Institute of Technology, 2012. http://hdl.handle.net/1853/50138.
Full textGhislieri, 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.
Full textRofouei, 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.
Full textJohansen, 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.
Full textHeuson, Egon. "Recherche de nouvelles transaminases pour la synthèse d'amines chirales." Thesis, Clermont-Ferrand 2, 2015. http://www.theses.fr/2015CLF22659/document.
Full textSlatter, 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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Graduate
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.
Full textLizier, 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.
Full textO presente trabalho investiga novos métodos analíticos para análise de aminas aromáticas selecionadas em virtude de suas proprideades toxicológicas e/ou mutagênicas em amostras de interesse ambiental usando técnicas cromatográficas com diversos detectores. Após otimização das condições cromatográficas as aminas aromáticas: 4,4'-oxidianilina, anilina, 2,4- diaminotoluidina, 4,4'-diaminobifenila, 4,4'-metileno-bis-(2-cloroanilina), 3,3'-diclorobenzidina, 2- aminonaftaleno, 2-metilanilina, 2-metoxianilina, 4,4'-diaminodifenilmetano, 2-cloro-4-nitroanilina, 4-aminobifenila, 2-metoxi-5-metilanilina, 3,3'-dimetoxibenzidina, 4-cloroanilina e 3,3'- diclorobenzidina apresentaram picos bem DEfinidos em fase móvel metanol/água 70:30 (v/v) e vazão de 0,8 ml min-1 classificadas como grupo I. As aminas 1,4-diaminobenzeno, 4,4'- metilbenzeno-1,4-diamina, p-aminofenol, N-monoacetil-1,4-diaminobenzeno, 2,5-dimetilanilina, 4,4'-metileno-bis-2-metilanilina e 4-cloro-2-metilanilina foram agrupadas no grupo II, melhor separadas em fase móvel acetonitrila/água 60:40 (v/v), vazão 0,8 ml min-1 e T= 40 C. A comparação entre os detectores de arranjo de diodos (DAD) e eletroquímico (ED) foram conduzidos nestas condições otimizadas e curvas analíticas lineares foram construídas para todas estas aminas entre 1 a 250 mg L-1 (detector DAD = 230 nm) e 0,5 a 250 mg L-1 (detector ED - Ep = +1,0V)), utilizando para isto a adição de 30 x 10-3 Mol L-1 do líquido iônico BMIm-NTf2 (1-butil-3-metilimidazólio de bis(trifluorometilsulfonil)imida). A adição do líquido iônico promoveu melhor separação e aumento na intensidade dos picos cromatográficos em ambos os detectores. O limite de detecção das aminas por HPLC-DAD e HPLC-ED mostraram valores entre 1,27 a 10,2 mg L-1 e 1,33 a 6,04 mg L-1, respectivamente. O limite de quantificação das aminas por HPLC-DAD e HPLC-ED mostraram valores entre 4,24 a 34,0 mg L-1 e 4,44 a 20,1 mg L-1, ...
This work investigates new analytical methods for analysis of aromatic amines selected because of their toxicological and/or mutagenic properties in samples of environmental interest using chromatographic techniques with various detectors. After optimization of chromatographic conditions as aromatic amines: 4,4'-oxydianiline, aniline, 2,4-diaminotoluidina, 4,4'- diaminobifenila, 4,4'-methylenebis-(2-chloroaniline), 3,3'-dichlorobenzidine, 2- aminonaphthalene, 2-methylaniline, 2-methoxyaniline, 4,4'-diaminodiphenylmethame, 2-chloro- 4-nitroaniline, 4-aminobifenila, 2-methoxy-5-methylaniline, 3,3'-dimethoxybenzidine, 4- chloroaniline and 3,3'-dichlorobenzidine showed well defined peaks in the mobile phase methanol/water 70:30 (v/v) and a flow rate of 0.8 mL min-1 classified as group I. The amines 1,4- diaminobenzene, 4,4'-methylbenzene-1,4-diamine, p-aminophenol, N-monoacethyl-1,4- diaminobenzene, 2,5-dimethylaniline, 4,4'-methylene-bis-2-methylaniline and 4-chloro-2- methylaniline were grouped in group II, best separated in the mobile phase acetonitrile/water 60:40 (v/v), flow rate 0.8 mL min-1 and T = 40°C. The comparison between the diode array detector (DAD) and electrochemical (ED) were conducted on these optimized conditions, linear calibration curves were constructed for all these amines from 1 to 250 mg L-1 (DAD detector = 230 nm) and 0.5 to 250 mg L-1 (detector ED - Ep = +1.0 V), using for this purpose the addition of 30 x 10-3 mol L-1 of BMIm-NTf2 ionic liquid (1-butyl-3-methylimidazolium-bis- (trifluoromethylsulfonyl)imide). The addition of ionic liquid promoted better separation and increase in the intensity of the chromatographic peaks in both detectors. The HPLC-DAD and HPLC-ED detection limit of the amines showed values between 1.27 to 10.2 mg L-1 and 1.33 to 6.04 mg L-1, respectively. The HPLC-DAD and HPLC-ED limit of quantification of the amines showed values between 4.24 to 34.0 mg L-1 and from 4.44 to 20.1 mg L-1,...
Books on the topic "Amines"
G, Baumgartner William, ed. Amines. Cleveland: Freedonia Group, 1998.
Find full textL, Hayes Teresa, Richardson Michael B, Friedman Rebecca L, and Freedonia Group, eds. Amines. Cleveland: Freedonia Group, 2000.
Find full textBoulton, A. A., A. V. Juorio, and R. G. H. Downer, eds. Trace Amines. Totowa, NJ: Humana Press, 1988. http://dx.doi.org/10.1007/978-1-4612-4602-2.
Full textBruno, Mondovì, ed. Structure and functions of amine oxidases. Boca Raton, Fla: CRC Press, 1985.
Find full textKagakkai, Nihon Bunseki. Aminosan, seitai amin bunseki. Tōkyō: Maruzen Shuppan, 2012.
Find full textBoulton, Alan A., Glen B. Baker, and Judith M. Baker. Amines and Their Metabolites. New Jersey: Humana Press, 1985. http://dx.doi.org/10.1385/0896030768.
Full textLi, Wei, and Xumu Zhang, eds. Stereoselective Formation of Amines. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53929-9.
Full textSaad, Bahruddin, and Rosanna Tofalo, eds. Biogenic Amines in Food. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015813.
Full textA, Boulton A., Baker Glen B. 1947-, and Baker Judith M, eds. Amines and their metabolites. Clifton, N.J: Humana Press, 1985.
Find full textFollain, Nadege. Amines grafted cellulose materials. New York: Nova Science Publishers, 2010.
Find full textBook chapters on the topic "Amines"
Börnick, Hilmar, and Torsten C. Schmidt. "Amines." In Organic Pollutants in the Water Cycle, 181–209. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/352760877x.ch8.
Full textGooch, Jan W. "Amines." In Encyclopedic Dictionary of Polymers, 35. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_555.
Full textTucker, William B. "Amines." In Organic Chemistry, 277–87. Boca Raton: CRC Press, 2024. http://dx.doi.org/10.1201/9781003479352-23.
Full textSourkes, T. L. "Copper, Biogenic Amines, and Amine Oxidases." In Novartis Foundation Symposia, 143–61. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470720622.ch8.
Full textYon, A. Marjorie, B. Jean-Daniel Marty, and C. Diana Ciuculescu-Pradines. "CHAPTER 6. Amines and Amine-boranes." In Reducing Agents in Colloidal Nanoparticle Synthesis, 130–56. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839163623-00130.
Full textKhan, JaVed I., Thomas J. Kennedy, and Donnell R. Christian. "Tertiary Amines." In Basic Principles of Forensic Chemistry, 177–90. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-59745-437-7_14.
Full textSahar, Amna, Ubaid ur Rahman, Muhammad Issa Khan, and Muhammad Azam Khan. "Heterocyclic Amines." In Food Safety, 89–111. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-39253-0_5.
Full textTuriault, Marc, Caroline Cohen, Guy Griebel, David E. Nichols, Britta Hahn, Gary Remington, Ronald F. Mucha, et al. "Trace Amines." In Encyclopedia of Psychopharmacology, 1325–29. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_211.
Full textTyrer, Peter J., Mark Slifstein, Joris C. Verster, Kim Fromme, Amee B. Patel, Britta Hahn, Christer Allgulander, et al. "Biogenic Amines." In Encyclopedia of Psychopharmacology, 227. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_598.
Full textTomlinson, Sara, Darrell D. Mousseau, Glen B. Baker, and Ashley D. Radomski. "Trace Amines." In Encyclopedia of Psychopharmacology, 1723–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-36172-2_211.
Full textConference papers on the topic "Amines"
Khramov, Dimitri, Balakrishnan Panamarathupalayam, and Evgeny Barmatov. "Demystifying Amine Inhibitor Chemistry." In SPE International Conference on Oilfield Chemistry. SPE, 2023. http://dx.doi.org/10.2118/213797-ms.
Full textFrizzo, Clarissa, Dionisia Sanz, José Elguero, and Rosa Claramunt. "Biotinylated Primary Amines." In The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00404.
Full textDiFlavio, John-Louis, Robert Bertoia, Robert Pelton, and Marc Leduc. "The Mechanism of Polyvinylamine Wet-strengthening." In Advances in Paper Science and Technology, edited by S. J. I’Anson. Fundamental Research Committee (FRC), Manchester, 2005. http://dx.doi.org/10.15376/frc.2005.2.1293.
Full textManabe, S., H. Yanagisawa, S. Ishikawa, Y. Kitagawa, K. Tohyama, S. Abe, and O. Wada. "TRYPTOPHAN PYROLYSIS PRODUCTS FOUND IN COOKED FOODS INHIBIT HUMAN PLATELET AGGREGATION BY INHIBITING CYCLOOXYGENASE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643402.
Full textAbbo, Hanna, Marvin Piet, Salam Titinchi, Wilhelm Schwieger, and Olav Bolland. "Amino-Functionalized Silica Materials for Carbon Dioxide Capture." In ASME 2015 9th International Conference on Energy Sustainability collocated with the ASME 2015 Power Conference, the ASME 2015 13th International Conference on Fuel Cell Science, Engineering and Technology, and the ASME 2015 Nuclear Forum. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/es2015-49743.
Full textKinaci, Emre, Giuseppe Palmese, Joseph Stanzione, and Sarah Salazar. "Evaluation of hybridized bio-based building blocks as coating materials." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/oyjf3899.
Full textLu, Dong, Alastair Trigg, Zhenxiang Xing, Rakesh Kumar, and Chang Kuo Chang. "Application of ToF-SIMS to Airborne Organic Contamination Analysis." In ISTFA 2003. ASM International, 2003. http://dx.doi.org/10.31399/asm.cp.istfa2003p0215.
Full textVazquez, O., T. Chen, L. Crombie, P. Chen, S. Heath, and Q. Guo. "The Impact of Pre-flush Additives on Scale Squeeze Treatments - Application of Modelling and New Test Methodologies to Understand Mechanisms of Retention and Optimise Field Treatment Designs." In SPE International Oilfield Scale Conference and Exhibition. SPE, 2014. http://dx.doi.org/10.2118/spe-169800-ms.
Full textKim, Hoon Sik, Minjeong Kim, and Minserk Cheong. "Functionalized Tertiary Amines as SO2 Absorbents." In The World Congress on Civil, Structural, and Environmental Engineering. Avestia Publishing, 2016. http://dx.doi.org/10.11159/icesdp16.112.
Full textEpure, Petru, Ana-Maria Gurban, and Lucian-Gabriel Zamfir. "Practical Aspects of Biogenic Amines Detection." In Priochem 2023. Basel Switzerland: MDPI, 2023. http://dx.doi.org/10.3390/chemproc2023013024.
Full textReports on the topic "Amines"
Selig, W. Determination of equivalent weight of amines. Office of Scientific and Technical Information (OSTI), January 1987. http://dx.doi.org/10.2172/6881693.
Full textThomson, 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), August 1993. http://dx.doi.org/10.2172/10180988.
Full textHameka, Hendrik F., George R. Famini, James O. Jensen, and E. I. Newhouse. Computations of Vibrational Infrared Frequencies of Selected Amines. Fort Belvoir, VA: Defense Technical Information Center, January 1990. http://dx.doi.org/10.21236/ada218840.
Full textMossine, Valerie V. Multivalent Lactulose-amines as Inhibitors of Prostate Cancer Metastasis. Fort Belvoir, VA: Defense Technical Information Center, March 2002. http://dx.doi.org/10.21236/ada406249.
Full textHameka, H. F., G. R. Famini, J. O. Jensen, and J. L. Jensen. Theoretical Prediction of Vibrational Infrared Frequencies of Tertiary Amines. Fort Belvoir, VA: Defense Technical Information Center, February 1991. http://dx.doi.org/10.21236/ada232880.
Full textOverly, Joyce, and Deanne Snavely. Vibrational Overtone Spectroscopy of Cyclic Amines: Pyridine and Related Compounds. Fort Belvoir, VA: Defense Technical Information Center, May 1993. http://dx.doi.org/10.21236/ada265524.
Full textAdams, R. The transformation of organic amines by transition metal cluster compounds. Office of Scientific and Technical Information (OSTI), February 1990. http://dx.doi.org/10.2172/7108222.
Full textFrechet, Jean M., and James F. Cameron. Photogenerated Amines and Diamines: Novel Curing Systems for Thin Film Coatings. Fort Belvoir, VA: Defense Technical Information Center, May 1991. http://dx.doi.org/10.21236/ada235568.
Full textAdams, R. D. The transformation of organic amines by transition metal cluster compounds: Progress report. Office of Scientific and Technical Information (OSTI), November 1994. http://dx.doi.org/10.2172/10105409.
Full textRosen, R. K. Reaction of Tris(cyclopentadienyl)uranium compounds with amines, azides, and related ligands. Office of Scientific and Technical Information (OSTI), December 1989. http://dx.doi.org/10.2172/7257519.
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