Auswahl der wissenschaftlichen Literatur zum Thema „Amides“
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Zeitschriftenartikel zum Thema "Amides":
Soong, Chee-Leong, Jun Ogawa und Sakayu Shimizu. „A Novel Amidase (Half-Amidase) for Half-Amide Hydrolysis Involved in the Bacterial Metabolism of Cyclic Imides“. Applied and Environmental Microbiology 66, Nr. 5 (01.05.2000): 1947–52. http://dx.doi.org/10.1128/aem.66.5.1947-1952.2000.
Barham, Joshua P., und Jaspreet Kaur. „Site-Selective C(sp3)–H Functionalizations Mediated by Hydrogen Atom Transfer Reactions via α-Amino/α-Amido Radicals“. Synthesis 54, Nr. 06 (25.10.2021): 1461–77. http://dx.doi.org/10.1055/a-1677-6619.
Zhou, Yongyun, Ruhima Khan, Baomin Fan und Lijin Xu. „Ruthenium-Catalyzed Selective Reduction of Carboxylic Esters and Carboxamides“. Synthesis 51, Nr. 12 (30.04.2019): 2491–505. http://dx.doi.org/10.1055/s-0037-1611524.
Zarecki, Adam P., Jacek L. Kolanowski und Wojciech T. Markiewicz. „Microwave-Assisted Catalytic Method for a Green Synthesis of Amides Directly from Amines and Carboxylic Acids“. Molecules 25, Nr. 8 (11.04.2020): 1761. http://dx.doi.org/10.3390/molecules25081761.
Orsy, György, Sayeh Shahmohammadi und Enikő Forró. „A Sustainable Green Enzymatic Method for Amide Bond Formation“. Molecules 28, Nr. 15 (28.07.2023): 5706. http://dx.doi.org/10.3390/molecules28155706.
Martinez-Rodríguez, Sergio, Rafael Contreras-Montoya, Jesús M. Torres, Luis Álvarez de Cienfuegos und Jose Antonio Gavira. „A New L-Proline Amide Hydrolase with Potential Application within the Amidase Process“. Crystals 12, Nr. 1 (23.12.2021): 18. http://dx.doi.org/10.3390/cryst12010018.
Khalimon, Andrey, Kristina Gudun und Davit Hayrapetyan. „Base Metal Catalysts for Deoxygenative Reduction of Amides to Amines“. Catalysts 9, Nr. 6 (28.05.2019): 490. http://dx.doi.org/10.3390/catal9060490.
Fournand, David, Frederic Bigey und Alain Arnaud. „Acyl Transfer Activity of an Amidase from Rhodococcussp. Strain R312: Formation of a Wide Range of Hydroxamic Acids“. Applied and Environmental Microbiology 64, Nr. 8 (01.08.1998): 2844–52. http://dx.doi.org/10.1128/aem.64.8.2844-2852.1998.
Ding, Wen, Shaoyu Mai und Qiuling Song. „Molecular-oxygen-promoted Cu-catalyzed oxidative direct amidation of nonactivated carboxylic acids with azoles“. Beilstein Journal of Organic Chemistry 11 (11.11.2015): 2158–65. http://dx.doi.org/10.3762/bjoc.11.233.
Meerakrishna, Ramakrishnan Suseela, und Ponnusamy Shanmugam. „Synthesis of blue-red emissive amido-substituted di(het)aryl and tri(het)aryl amine derivatives via chemoselective N-mono and N,N-diarylation of (het) aryl amino amides using benzyne/arynes“. New Journal of Chemistry 43, Nr. 6 (2019): 2550–58. http://dx.doi.org/10.1039/c8nj05823g.
Dissertationen zum Thema "Amides":
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.
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.
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.
Muller, Catherine R. „Lithium amides in synthesis“. Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.413176.
Richardson, J. „Corrosion inhibition with amides“. Thesis, University of Nottingham, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381056.
Ledingham, Lyndsay A. „Sustainable methods for the chemical synthesis of amides and amide-containing aromatic compounds“. Thesis, University of York, 2016. http://etheses.whiterose.ac.uk/16191/.
Lauck, Maximilian Thomas Johannes [Verfasser]. „Cobaltocenium Amides - Photoinduced Electron Transfer Processes in Donor-Acceptor Amides / Maximilian Thomas Johannes Lauck“. Mainz : Universitätsbibliothek Mainz, 2020. http://d-nb.info/1205943900/34.
Farrell, Emma K. „Biosynthesis of fatty acid amides“. Scholar Commons, 2010. http://scholarcommons.usf.edu/etd/1629.
Lineswala, Jayana P. „Total synthesis of lavendamycin amides“. Virtual Press, 1996. http://liblink.bsu.edu/uhtbin/catkey/1036197.
Department of Chemistry
McCarthy, Sean Joseph. „Strained amides as potential antibacterials“. Thesis, University of Sussex, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296003.
Bücher zum Thema "Amides":
Arthur, Greenberg, Breneman Curt M und Liebman Joel F, Hrsg. The amide linkage: Structural significance in chemistry, biochemistry, and materials science. Hoboken, NJ: Wiley-Interscience, 2003.
Arthur, Greenberg, Breneman Curt M und Liebman Joel F, Hrsg. The amide linkage: Selected structural aspects in chemistry, biochemistry, and materials science. New York: Wiley-Interscience, 2000.
Westlund, Neil Edward. Atropisomerism in hindered tertiary amides. Manchester: University of Manchester, 1996.
Relihan, Colette. 1-Hydroxy-1-aminoalkenes: Enols of amides. Dublin: University College Dublin, 1998.
Hickey, Kenneth. A study of amides in aqueous and non-aqueous solution. Dublin: University College Dublin, 1995.
Mazurkiewicz, Roman. Studium reakcji imidoilowania amidów. Gliwice: Politechnika Śląska, 1989.
Lemmerer, Miran. Chemoselective Nucleophilic α-Amination of Amides. Wiesbaden: Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-30020-3.
Hutchby, Marc. Novel Synthetic Chemistry of Ureas and Amides. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32051-4.
Bukowska, Jolanta. Spektroskopia oscylacyjna roztworów amidowych. Warszawa: Wydawnictwa Uniwersytetu Warszawskiego, 1986.
Kolev, Tsonko. Quantum chemical, spectroscopic and structural study of hydrochlorides, hydrogens squarates and ester amides of squaric acid of amina. New York: Nova Science Publishers, 2008.
Buchteile zum Thema "Amides":
Paulus, Wilfried. „Amides“. In Microbicides for the Protection of Materials, 241–64. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2118-7_10.
Gooch, Jan W. „Amides“. In Encyclopedic Dictionary of Polymers, 33. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_546.
Paulus, Wilfried. „Amides“. In Directory of Microbicides for the Protection of Materials, 608–18. Dordrecht: Springer Netherlands, 2004. http://dx.doi.org/10.1007/1-4020-2818-0_33.
Smith, Robert M., und Arthur E. Martell. „Amides“. In Critical Stability Constants, 423–25. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4615-6764-6_23.
Sonke, Theo, und Bernard Kaptein. „Hydrolysis of Amides“. In Enzyme Catalysis in Organic Synthesis, 561–650. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639861.ch15.
Lappert, M. F. „From Organotin Amides“. In Inorganic Reactions and Methods, 353–54. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145234.ch139.
Lappert, M. F. „From Organolead Amides“. In Inorganic Reactions and Methods, 396. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145234.ch160.
Carmalt, Claire J., Neville A. Compton, R. John Errington, George A. Fisher, Ismunaryo Moenandar, Nicholas C. Norman und Kenton H. Whitmire. „Homoleptic Bismuth Amides“. In Inorganic Syntheses, 98–101. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132623.ch15.
Ouellette, Robert J., und J. David Rawn. „Amines and Amides“. In Organic Chemistry, 763–800. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-12-812838-1.50024-4.
Ouellette, Robert J., und J. David Rawn. „Amines and Amides“. In Principles of Organic Chemistry, 315–42. Elsevier, 2015. http://dx.doi.org/10.1016/b978-0-12-802444-7.00012-4.
Konferenzberichte zum Thema "Amides":
Moraes, Fernanda C., Elson S. Alvarenga und Kariny B. Amorim. „Synthesis of novel amides derived from lumisantonin“. In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201391315423.
Anastopoulos, G., E. Lois, A. Serdari, S. Stournas, F. Zannikos und S. Kalligeros. „The Impact of Aliphatic Amines and Tertiary Amides on the Lubrication Properties of Ultra Low Sulfur Diesel Fuels“. In CEC/SAE Spring Fuels & Lubricants Meeting & Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2000. http://dx.doi.org/10.4271/2000-01-1916.
Jones, Saul, und Daniel Credgington. „Exploring the photophysics of carbene metal amides (Conference Presentation)“. In Organic Light Emitting Materials and Devices XXII, herausgegeben von Franky So, Chihaya Adachi und Jang-Joo Kim. SPIE, 2018. http://dx.doi.org/10.1117/12.2322372.
Poku, Rosemary Aniwaa, Augustine Nkembo, Olufisayo Salako, Felix Amissah, Hernan Flores-Rozas, Tryphon Mazu und Nazarius S. Lamango. „Abstract 5090: Targeting metastatic prostate cancer with polyisoprenylated cysteinyl amides“. In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-5090.
Musiol, Robert, Jaroslaw Polanski, Jiri Dohnal, Violetta Kozik, Barbara Podeszwa, Jacek Finster, Dominik Tabak, Katarina Kralova und Josef Jampilek. „Preparation and Herbicidal Activities of Substituted Amides of Quinoline Derivatives“. In The 11th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01308.
Gouvêa, Venise A., José C. Campos, Juliano Bosenbecker, Anaí Duarte, Rogério A. Freitag, Claudio M. P. Pereira und Geonir M. Siqueira. „Synthesis of amides and thioesteres derivatives, precursors to heterocyclic thiazolidinones“. In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0052-1.
Cavalcante Silva, S., J. H. Batista, Moraes F., N. de A. Pereira und G. C. Clososki. „Directed Metalation of Aromatic Aldimines Using Li/Mg-TMP Amides“. In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013926134127.
Gladkova, Elizaveta, Arina Chepanova, Alexandra Zakharenko und Olga Luzina. „New sulfonates and amides derived from berberine as Tdp1 inhibitors“. In 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07464.
Gunawan, Erin Ryantin, Dedy Suhendra und Dewi Sinta. „Profile of fatty acid amides synthesized from ketapang kernel oil“. In THE 9TH INTERNATIONAL CONFERENCE OF THE INDONESIAN CHEMICAL SOCIETY ICICS 2021: Toward a Meaningful Society. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0106337.
Udhayasurian, R., K. Sivakumar, A. M. Sajith und Muthipeedika Nibin Joy. „Synthesis of some pharmacologically relevant coumarins linked with (hetero)aryl amides“. In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018033.
Berichte der Organisationen zum Thema "Amides":
Jiang, Zhiping, Leonard V. Interrante, Daekeun Kwon, Fook S. Tham und Rudy Kullnig. Synthesis, Structure and Pyrolysis of Organoaluminum Amides Derived from the Reaction of Trialkylaluminum Compounds with Ethylenediamine in a 3:2 Ration. Fort Belvoir, VA: Defense Technical Information Center, August 1990. http://dx.doi.org/10.21236/ada225758.
Castner, E. W. Temperature-dependence of the ultrafast intermolecular dynamics of Amides: Formamide, N-methylformamide, N,N-dimethylformamide, N- methylacetamide, and N-methylpropionamide from 290-370 K. Office of Scientific and Technical Information (OSTI), Juni 1996. http://dx.doi.org/10.2172/249036.
Lin, Terri C. Poly(amido amine) Dendrimers in Supercapacitors. Office of Scientific and Technical Information (OSTI), August 2013. http://dx.doi.org/10.2172/1091321.
Fernando, P. U. Ashvin Iresh, Gilbert Kosgei, Matthew Glasscott, Garrett George, Erik Alberts und Lee Moores. Boronic acid functionalized ferrocene derivatives towards fluoride sensing. Engineer Research and Development Center (U.S.), Juli 2022. http://dx.doi.org/10.21079/11681/44762.
Whitaker, Craig, Jay R. Heckert und Ian C. Uber. Synthesis of Amide Functionalized Carbon Nanotubes. Fort Belvoir, VA: Defense Technical Information Center, Januar 2007. http://dx.doi.org/10.21236/ada519137.
Thomson, J. S., J. B. Green, T. B. McWilliams und 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.
Hameka, Hendrik F., George R. Famini, James O. Jensen und E. I. Newhouse. Computations of Vibrational Infrared Frequencies of Selected Amines. Fort Belvoir, VA: Defense Technical Information Center, Januar 1990. http://dx.doi.org/10.21236/ada218840.
Mossine, Valerie V. Multivalent Lactulose-amines as Inhibitors of Prostate Cancer Metastasis. Fort Belvoir, VA: Defense Technical Information Center, März 2002. http://dx.doi.org/10.21236/ada406249.
Hameka, H. F., G. R. Famini, J. O. Jensen und J. L. Jensen. Theoretical Prediction of Vibrational Infrared Frequencies of Tertiary Amines. Fort Belvoir, VA: Defense Technical Information Center, Februar 1991. http://dx.doi.org/10.21236/ada232880.
Niles, Keron. Resilience Amidst Rising Tides. Geneva, Switzerland: International Centre for Trade and Sustainable Development, 2010. http://dx.doi.org/10.7215/co_ip_20100224.