Literatura académica sobre el tema "Amines"
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Artículos de revistas sobre el tema "Amines"
Budynina, Ekaterina, Konstantin Ivanov, Ivan Sorokin y Mikhail Melnikov. "Ring Opening of Donor–Acceptor Cyclopropanes with N-Nucleophiles". Synthesis 49, n.º 14 (18 de mayo de 2017): 3035–68. http://dx.doi.org/10.1055/s-0036-1589021.
Texto completoBarham, Joshua P. y Jaspreet Kaur. "Site-Selective C(sp3)–H Functionalizations Mediated by Hydrogen Atom Transfer Reactions via α-Amino/α-Amido Radicals". Synthesis 54, n.º 06 (25 de octubre de 2021): 1461–77. http://dx.doi.org/10.1055/a-1677-6619.
Texto completoManthey, MK, SG Pyne y RJW Truscott. "Addition of Aliphatic and Aromatic Amines to Catechol in Aqueous Solution Under Oxidizing Conditions". Australian Journal of Chemistry 42, n.º 3 (1989): 365. http://dx.doi.org/10.1071/ch9890365.
Texto completoOs, Van M., Van A. M. Vuuren y S. F. Spoelstra. "Mechanisms of adaptation in sheep to overcome silage intake depression induced by biogenic amines". British Journal of Nutrition 77, n.º 3 (marzo de 1997): 399–415. http://dx.doi.org/10.1079/bjn19970041.
Texto completoSaha, Sayantani y Moris S. Eisen. "Mild catalytic deoxygenation of amides promoted by thorium metallocene". Dalton Transactions 49, n.º 36 (2020): 12835–41. http://dx.doi.org/10.1039/d0dt02770g.
Texto completoYedage, Subhash L., Denvert S. D'silva y Bhalchandra M. Bhanage. "MnO2 catalyzed formylation of amines and transamidation of amides under solvent-free conditions". RSC Advances 5, n.º 98 (2015): 80441–49. http://dx.doi.org/10.1039/c5ra13094h.
Texto completoLeggio, A., E. L. Belsito, G. De Luca, M. L. Di Gioia, V. Leotta, E. Romio, C. Siciliano y A. Liguori. "One-pot synthesis of amides from carboxylic acids activated using thionyl chloride". RSC Advances 6, n.º 41 (2016): 34468–75. http://dx.doi.org/10.1039/c5ra24527c.
Texto completoZhang, Qiao, Xiao-Tao Lin, Norihisa Fukaya, Tadahiro Fujitani, Kazuhiko Sato y 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, n.º 23 (2020): 8414–22. http://dx.doi.org/10.1039/d0gc02890h.
Texto completoCharron, Carlie L., Jade M. Cottam Jones y Craig A. Hutton. "Are Aminomethyl Thioesters Viable Intermediates in Native Chemical Ligation Type Amide Bond Forming Reactions?" Australian Journal of Chemistry 71, n.º 9 (2018): 697. http://dx.doi.org/10.1071/ch18198.
Texto completoYao, 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, n.º 22 (23 de noviembre de 2016): 14527–43. http://dx.doi.org/10.5194/acp-16-14527-2016.
Texto completoTesis sobre el tema "Amines"
Sandford, Graham. "Some amine hydrofluorides and amines in organofluorine chemistry". Thesis, Durham University, 1991. http://etheses.dur.ac.uk/6209/.
Texto completoKargina, Irina. "Topochemical reactions of amines and amides with titanium and vanadium oxychlorides". Thesis, University of Ottawa (Canada), 1995. http://hdl.handle.net/10393/10109.
Texto completoAbrahamson, Michael J. "Development of an amine dehydrogenase". Diss., Georgia Institute of Technology, 2012. http://hdl.handle.net/1853/50138.
Texto completoGhislieri, 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.
Texto completoRofouei, 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.
Texto completoJohansen, 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.
Texto completoHeuson, Egon. "Recherche de nouvelles transaminases pour la synthèse d'amines chirales". Thesis, Clermont-Ferrand 2, 2015. http://www.theses.fr/2015CLF22659/document.
Texto completoSlatter, John Gregory. "Metabolism of tertiary arylaliphatic amines and formamides in rats". Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/29392.
Texto completoPharmaceutical Sciences, Faculty of
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.
Texto completoLizier, 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.
Texto completoO 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,...
Libros sobre el tema "Amines"
G, Baumgartner William, ed. Amines. Cleveland: Freedonia Group, 1998.
Buscar texto completoL, Hayes Teresa, Richardson Michael B, Friedman Rebecca L y Freedonia Group, eds. Amines. Cleveland: Freedonia Group, 2000.
Buscar texto completoBoulton, A. A., A. V. Juorio y R. G. H. Downer, eds. Trace Amines. Totowa, NJ: Humana Press, 1988. http://dx.doi.org/10.1007/978-1-4612-4602-2.
Texto completoBruno, Mondovì, ed. Structure and functions of amine oxidases. Boca Raton, Fla: CRC Press, 1985.
Buscar texto completoKagakkai, Nihon Bunseki. Aminosan, seitai amin bunseki. Tōkyō: Maruzen Shuppan, 2012.
Buscar texto completoBoulton, Alan A., Glen B. Baker y Judith M. Baker. Amines and Their Metabolites. New Jersey: Humana Press, 1985. http://dx.doi.org/10.1385/0896030768.
Texto completoLi, Wei y Xumu Zhang, eds. Stereoselective Formation of Amines. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-53929-9.
Texto completoSaad, Bahruddin y Rosanna Tofalo, eds. Biogenic Amines in Food. Cambridge: Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015813.
Texto completoA, Boulton A., Baker Glen B. 1947- y Baker Judith M, eds. Amines and their metabolites. Clifton, N.J: Humana Press, 1985.
Buscar texto completoFollain, Nadege. Amines grafted cellulose materials. New York: Nova Science Publishers, 2010.
Buscar texto completoCapítulos de libros sobre el tema "Amines"
Börnick, Hilmar y Torsten C. Schmidt. "Amines". En 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.
Texto completoGooch, Jan W. "Amines". En Encyclopedic Dictionary of Polymers, 35. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_555.
Texto completoTucker, William B. "Amines". En Organic Chemistry, 277–87. Boca Raton: CRC Press, 2024. http://dx.doi.org/10.1201/9781003479352-23.
Texto completoSourkes, T. L. "Copper, Biogenic Amines, and Amine Oxidases". En Novartis Foundation Symposia, 143–61. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470720622.ch8.
Texto completoYon, A. Marjorie, B. Jean-Daniel Marty y C. Diana Ciuculescu-Pradines. "CHAPTER 6. Amines and Amine-boranes". En Reducing Agents in Colloidal Nanoparticle Synthesis, 130–56. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839163623-00130.
Texto completoKhan, JaVed I., Thomas J. Kennedy y Donnell R. Christian. "Tertiary Amines". En Basic Principles of Forensic Chemistry, 177–90. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-59745-437-7_14.
Texto completoSahar, Amna, Ubaid ur Rahman, Muhammad Issa Khan y Muhammad Azam Khan. "Heterocyclic Amines". En Food Safety, 89–111. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-39253-0_5.
Texto completoTuriault, Marc, Caroline Cohen, Guy Griebel, David E. Nichols, Britta Hahn, Gary Remington, Ronald F. Mucha et al. "Trace Amines". En Encyclopedia of Psychopharmacology, 1325–29. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_211.
Texto completoTyrer, Peter J., Mark Slifstein, Joris C. Verster, Kim Fromme, Amee B. Patel, Britta Hahn, Christer Allgulander et al. "Biogenic Amines". En Encyclopedia of Psychopharmacology, 227. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_598.
Texto completoTomlinson, Sara, Darrell D. Mousseau, Glen B. Baker y Ashley D. Radomski. "Trace Amines". En Encyclopedia of Psychopharmacology, 1723–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-36172-2_211.
Texto completoActas de conferencias sobre el tema "Amines"
Khramov, Dimitri, Balakrishnan Panamarathupalayam y Evgeny Barmatov. "Demystifying Amine Inhibitor Chemistry". En SPE International Conference on Oilfield Chemistry. SPE, 2023. http://dx.doi.org/10.2118/213797-ms.
Texto completoFrizzo, Clarissa, Dionisia Sanz, José Elguero y Rosa Claramunt. "Biotinylated Primary Amines". En The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00404.
Texto completoDiFlavio, John-Louis, Robert Bertoia, Robert Pelton y Marc Leduc. "The Mechanism of Polyvinylamine Wet-strengthening". En Advances in Paper Science and Technology, editado por S. J. I’Anson. Fundamental Research Committee (FRC), Manchester, 2005. http://dx.doi.org/10.15376/frc.2005.2.1293.
Texto completoManabe, S., H. Yanagisawa, S. Ishikawa, Y. Kitagawa, K. Tohyama, S. Abe y O. Wada. "TRYPTOPHAN PYROLYSIS PRODUCTS FOUND IN COOKED FOODS INHIBIT HUMAN PLATELET AGGREGATION BY INHIBITING CYCLOOXYGENASE". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643402.
Texto completoAbbo, Hanna, Marvin Piet, Salam Titinchi, Wilhelm Schwieger y Olav Bolland. "Amino-Functionalized Silica Materials for Carbon Dioxide Capture". En 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.
Texto completoKinaci, Emre, Giuseppe Palmese, Joseph Stanzione y Sarah Salazar. "Evaluation of hybridized bio-based building blocks as coating materials". En 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/oyjf3899.
Texto completoLu, Dong, Alastair Trigg, Zhenxiang Xing, Rakesh Kumar y Chang Kuo Chang. "Application of ToF-SIMS to Airborne Organic Contamination Analysis". En ISTFA 2003. ASM International, 2003. http://dx.doi.org/10.31399/asm.cp.istfa2003p0215.
Texto completoVazquez, O., T. Chen, L. Crombie, P. Chen, S. Heath y 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". En SPE International Oilfield Scale Conference and Exhibition. SPE, 2014. http://dx.doi.org/10.2118/spe-169800-ms.
Texto completoKim, Hoon Sik, Minjeong Kim y Minserk Cheong. "Functionalized Tertiary Amines as SO2 Absorbents". En The World Congress on Civil, Structural, and Environmental Engineering. Avestia Publishing, 2016. http://dx.doi.org/10.11159/icesdp16.112.
Texto completoEpure, Petru, Ana-Maria Gurban y Lucian-Gabriel Zamfir. "Practical Aspects of Biogenic Amines Detection". En Priochem 2023. Basel Switzerland: MDPI, 2023. http://dx.doi.org/10.3390/chemproc2023013024.
Texto completoInformes sobre el tema "Amines"
Selig, W. Determination of equivalent weight of amines. Office of Scientific and Technical Information (OSTI), enero de 1987. http://dx.doi.org/10.2172/6881693.
Texto completoThomson, J. S., J. B. Green, T. B. McWilliams y S. K. T. Yu. GC/MS determination of amines following exhaustive trifluoroacetylation. Office of Scientific and Technical Information (OSTI), agosto de 1993. http://dx.doi.org/10.2172/10180988.
Texto completoHameka, Hendrik F., George R. Famini, James O. Jensen y E. I. Newhouse. Computations of Vibrational Infrared Frequencies of Selected Amines. Fort Belvoir, VA: Defense Technical Information Center, enero de 1990. http://dx.doi.org/10.21236/ada218840.
Texto completoMossine, Valerie V. Multivalent Lactulose-amines as Inhibitors of Prostate Cancer Metastasis. Fort Belvoir, VA: Defense Technical Information Center, marzo de 2002. http://dx.doi.org/10.21236/ada406249.
Texto completoHameka, H. F., G. R. Famini, J. O. Jensen y J. L. Jensen. Theoretical Prediction of Vibrational Infrared Frequencies of Tertiary Amines. Fort Belvoir, VA: Defense Technical Information Center, febrero de 1991. http://dx.doi.org/10.21236/ada232880.
Texto completoOverly, Joyce y Deanne Snavely. Vibrational Overtone Spectroscopy of Cyclic Amines: Pyridine and Related Compounds. Fort Belvoir, VA: Defense Technical Information Center, mayo de 1993. http://dx.doi.org/10.21236/ada265524.
Texto completoAdams, R. The transformation of organic amines by transition metal cluster compounds. Office of Scientific and Technical Information (OSTI), febrero de 1990. http://dx.doi.org/10.2172/7108222.
Texto completoFrechet, Jean M. y James F. Cameron. Photogenerated Amines and Diamines: Novel Curing Systems for Thin Film Coatings. Fort Belvoir, VA: Defense Technical Information Center, mayo de 1991. http://dx.doi.org/10.21236/ada235568.
Texto completoAdams, R. D. The transformation of organic amines by transition metal cluster compounds: Progress report. Office of Scientific and Technical Information (OSTI), noviembre de 1994. http://dx.doi.org/10.2172/10105409.
Texto completoRosen, R. K. Reaction of Tris(cyclopentadienyl)uranium compounds with amines, azides, and related ligands. Office of Scientific and Technical Information (OSTI), diciembre de 1989. http://dx.doi.org/10.2172/7257519.
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