Gotowa bibliografia na temat „Ketones”
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Artykuły w czasopismach na temat "Ketones"
Qiao, Yue, Zhaohua Gao, Yong Liu, Yan Cheng, Mengxiao Yu, Lingling Zhao, Yixiang Duan i Yu Liu. "Breath Ketone Testing: A New Biomarker for Diagnosis and Therapeutic Monitoring of Diabetic Ketosis". BioMed Research International 2014 (2014): 1–5. http://dx.doi.org/10.1155/2014/869186.
Pełny tekst źródłaTaylor, Robert M., i Justin T. Baca. "Feasibility of Interstitial Fluid Ketone Monitoring with Microneedles". Metabolites 12, nr 5 (10.05.2022): 424. http://dx.doi.org/10.3390/metabo12050424.
Pełny tekst źródłaBasdevant, Benoit, Audrey-Anne Guilbault, Samuel Beaulieu, Antoine Jobin-Des Lauriers i Claude Y. Legault. "Iodine(III)-mediated synthesis of chiral α-substituted ketones: recent advances and mechanistic insights". Pure and Applied Chemistry 89, nr 6 (27.06.2017): 781–89. http://dx.doi.org/10.1515/pac-2016-1212.
Pełny tekst źródłaGoffinet, Line, Thierry Barrea, Véronique Beauloye i Philippe A. Lysy. "Blood versus urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study". Therapeutic Advances in Endocrinology and Metabolism 8, nr 1-2 (13.12.2016): 3–13. http://dx.doi.org/10.1177/2042018816681706.
Pełny tekst źródłaDong, Guangbin, Hee Lim i Dong Xing. "Transition-Metal-Catalyzed Ketone α-Alkylation and Alkenylation with Simple Alkenes and Alkynes through a Dual Activation Strategy". Synlett 30, nr 06 (21.11.2018): 674–84. http://dx.doi.org/10.1055/s-0037-1610315.
Pełny tekst źródłaMa, Shuai, Yunyun Li, Rigu Su, Jianxun Wu, Lingyuan Xie, Junshi Tang, Xusheng Wang i in. "Ketones in Low-Temperature Oxidation Products of Crude Oil". Processes 11, nr 6 (30.05.2023): 1664. http://dx.doi.org/10.3390/pr11061664.
Pełny tekst źródłaJanuś, E., i D. Borkowska. "Occurrence of ketone bodies in the urine of cows during the first three months after calving and their association with milk yield". Archives Animal Breeding 56, nr 1 (10.10.2013): 581–88. http://dx.doi.org/10.7482/0003-9438-56-057.
Pełny tekst źródłaBentourkia, M'hamed, Sébastien Tremblay, Fabien Pifferi, Jacques Rousseau, Roger Lecomte i Stephen Cunnane. "PET study of 11C-acetoacetate kinetics in rat brain during dietary treatments affecting ketosis". American Journal of Physiology-Endocrinology and Metabolism 296, nr 4 (kwiecień 2009): E796—E801. http://dx.doi.org/10.1152/ajpendo.90644.2008.
Pełny tekst źródłaBabu, Kaki Raveendra, Xin He i Silong Xu. "Lewis Base Catalysis Based on Homoconjugate Addition: Rearrangement of Electron-Deficient Cyclopropanes and Their Derivatives". Synlett 31, nr 02 (20.11.2019): 117–24. http://dx.doi.org/10.1055/s-0039-1690753.
Pełny tekst źródłaWood, Thomas R., Brianna J. Stubbs i Sandra E. Juul. "Exogenous Ketone Bodies as Promising Neuroprotective Agents for Developmental Brain Injury". Developmental Neuroscience 40, nr 5-6 (2018): 451–62. http://dx.doi.org/10.1159/000499563.
Pełny tekst źródłaRozprawy doktorskie na temat "Ketones"
Stubbs, Brianna. "Metabolism of exogenous ketones". Thesis, University of Oxford, 2016. https://ora.ox.ac.uk/objects/uuid:3a3f65b4-4442-415e-b4bc-e0175adf65b5.
Pełny tekst źródłaLateef, Juma. "The reactions of fluorinated ketones". Thesis, Brunel University, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.286819.
Pełny tekst źródłaSmith, Athene Rachael Cecilia. "Catalytic asymmetric reduction of ketones". Thesis, University of Warwick, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302649.
Pełny tekst źródłaGemmell, Natasha. "Diastereocontrolled modifications of sugar ketones". Thesis, University of Reading, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.342107.
Pełny tekst źródłaStudley, John Richard. "The asymmetric reduction of ketones". Thesis, University of Bath, 1996. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307117.
Pełny tekst źródłaZhu, Jia Liang. "Reductive alkylation of Ã-cyano ketones". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/nq39611.pdf.
Pełny tekst źródłaZinovyeva, Lyudmyla. "Darstellung und Reaktionen einiger ß,Y-ungesättigter Ketone - Preparation and reactivity of some ß,Y-unsaturated ketones". Gerhard-Mercator-Universitaet Duisburg, 2003. http://www.ub.uni-duisburg.de/ETD-db/theses/available/duett-09182003-170256/.
Pełny tekst źródłaEarlywine, Arthur Dale. "The stereochemistry and mechanism of the iron pentacarbonyl-promoted coupling of strained olefins to carbon monoxide : a NMR-facilitated study of the equilibrium constants between and collision complex of a 10,11-diphenyl-1,4:5,8-dimethano-1,4,4a,4b,5,8,8a, 8b-octahydrofluorene-9-one stereoisomer and the lanthanide shift reagent Eu(fod), the electrophilic aromatic thallation of some selected biomolecules, and the synthesis and high resolution NMR study of the two series of 1,4,4a,8a-tetrahydro-endo-1,4-methanonaphthalene-5 ,8-diones and pentacyclo[5.4.0.0,.0". Full-text version available from OU Domain via ProQuest Digital Dissertations, 1985.
Znajdź pełny tekst źródłaCanbolat, Eylem. "Organocatalytic Resolution Of Racemic Alpha Azido Ketones". Master's thesis, METU, 2012. http://etd.lib.metu.edu.tr/upload/12614602/index.pdf.
Pełny tekst źródła-azido compounds were synthesized according to literature. The acidic alpha-protons do not require strong bases. Their enantioselective deracemization and deracemization processes were screened by using Cinchona derivatives as organocatalysts. This screening process was monitored by chiral HPLC columns. The parameters such as catalyst loading, solvent, temperature, reaction time and additives were optimized to obtain high enantioselectivities up to 98%. In addition to deracemization reactions, Michael addition reactions were also performed by starting from &alpha
-azido chromanones. In these reactions different type of urea catalyst was used to activate the electrophilic part of trans-&beta
-nitrostyrene compound. Again by controlling the temperature, time and catalyst loading, two diastereomers were formed and the screening process was monitored by chiral HPLC columns again. The Michael products were obtained in up to 94% ee and 75% yield.
Bena, Luvuyo Clifford. "Investigations into the asymmetric reduction of ketones". Thesis, University of Port Elizabeth, 2003. http://hdl.handle.net/10948/323.
Pełny tekst źródłaKsiążki na temat "Ketones"
McGarraghy, Michelle. Ketones and isocyanates: Conerted catalysis. Dublin: University College Dublin, 1996.
Znajdź pełny tekst źródłaMason, Craig. Hydrazinolysis of cyclic [alpha]-nitro ketones. Sudbury, Ont: Laurentian University, 1993.
Znajdź pełny tekst źródłaVenner, Mark Ralph William. Studies in deracemisation of racemic ketones. Birmingham: Universityof Birmingham, 1992.
Znajdź pełny tekst źródłaUnited States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. 2-hexanona. Atlanta, GA: Departamento de Salud y Servicios Humanos de los EE.UU., Servicio de Salud Pública, Agencia para Sustancias Tóxicos y el Registro de Enfermedades, 1992.
Znajdź pełny tekst źródłaUnited States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Isoforona. Atlanta, Ga.]: Agencia para Sustancias Tóxicas y el Registro de Enfermedades, División de Toxicología, Departamento de Salud y Servicios Humanos de los EE.UU., Servicio de Salud Pública, 1989.
Znajdź pełny tekst źródłaUnited States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Isophorone. Atlanta, Ga]: U.S. Dept. of Health and Human Services, Agency for Toxic Substances and Disease Registry, Division of Toxicology, 2003.
Znajdź pełny tekst źródłaWalsh, Sinead M. The tautomerisation and isomerisation of [alpha]-heterocyclic ketones. Dublin: University College Dublin, 1998.
Znajdź pełny tekst źródłaNispen, Reinier van. Photochemistry and spectroscopy of some steroidal [beta], [gamma]-unsaturated ketones: A geometry-photoreactivity study. Alblasserdam: Offsetdrukkerij Haveka B.V., 1992.
Znajdź pełny tekst źródłaReisinger, Corinna. Epoxidations and Hydroperoxidations of α,β-Unsaturated Ketones. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-28118-1.
Pełny tekst źródłaGmehling, JÜrgen. Vapor-liquid equilibrium data collection: Ketones : supplement 1. Frankfurt-am-Main: DECHEMA, 1993.
Znajdź pełny tekst źródłaCzęści książek na temat "Ketones"
Gooch, Jan W. "Ketones". W Encyclopedic Dictionary of Polymers, 410. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6646.
Pełny tekst źródłaPoff, Angela M., Shannon L. Kesl, Andrew P. Koutnik, Sara E. Moss, Christopher Q. Rogers i Dominic P. D’Agostino. "Ketone Supplementation for Health and Disease". W Ketogenic Diet and Metabolic Therapies, redaktorzy Susan A. Masino, Detlev Boison, Dominic P. D’Agostino, Eric H. Kossoff i Jong M. Rho, 392–422. Oxford University Press, 2022. http://dx.doi.org/10.1093/med/9780197501207.003.0033.
Pełny tekst źródłaCaprio, V. "Ketones: Dialkyl Ketones". W Comprehensive Organic Functional Group Transformations II, 135–214. Elsevier, 2005. http://dx.doi.org/10.1016/b0-08-044655-8/00049-0.
Pełny tekst źródłaParkes, Kevin E. B., i Stewart K. Richardson. "Ketones: Dialkyl Ketones". W Comprehensive Organic Functional Group Transformations, 111–204. Elsevier, 1995. http://dx.doi.org/10.1016/b0-08-044705-8/00165-5.
Pełny tekst źródłaBurrows, Andrew, John Holman, Simon Lancaster, Tina Overton, Andrew Parsons, Gwen Pilling i Gareth Price. "Aldehydes and ketones". W Chemistry3. Oxford University Press, 2021. http://dx.doi.org/10.1093/hesc/9780198829980.003.0023.
Pełny tekst źródłaJones, John. "Reactions of amino compounds with aldehydes and ketones". W Core Carbonyl Chemistry. Oxford University Press, 1997. http://dx.doi.org/10.1093/hesc/9780198559597.003.0004.
Pełny tekst źródłaD’Agostino, Dominic P. "Overview". W Ketogenic Diet and Metabolic Therapies, redaktorzy Susan A. Masino, Detlev Boison, Dominic P. D’Agostino, Eric H. Kossoff i Jong M. Rho, 389–91. Oxford University Press, 2022. http://dx.doi.org/10.1093/med/9780197501207.003.0032.
Pełny tekst źródła"Ketones". W Lead Optimization for Medicinal Chemists, 139–43. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527645640.ch30.
Pełny tekst źródłaGraedel, T. E., Donald T. Hawkins i Larry D. Claxton. "Ketones". W Atmospheric Chemical Compounds, 260–94. Elsevier, 1986. http://dx.doi.org/10.1016/b978-0-08-091842-6.50009-7.
Pełny tekst źródłaSandler, Stanley R., i Wolf Karo. "KETONES". W Sourcebook of Advanced Organic Laboratory Preparations, 53–57. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-08-092553-0.50012-1.
Pełny tekst źródłaStreszczenia konferencji na temat "Ketones"
Preses, J. M., G. E. Hall, J. T. Muckerman i R. E. Weston. "Time-resolved Fourier-transform Infrared Emission Study of the 193-nm Photolysis of 3-Pentanone". W Fourier Transform Spectroscopy. Washington, D.C.: Optica Publishing Group, 1995. http://dx.doi.org/10.1364/fts.1995.ffd11.
Pełny tekst źródłaGeslin, Alexis, Clément Paul, Philippe Bussi, Robert Barsotti, Jonathon Hollahan i Mary Calvin. "PEKK Poly Ether Ketone Ketone for High Temperature High Pressure Oil & Gas Conditions". W Offshore Technology Conference. OTC, 2021. http://dx.doi.org/10.4043/30987-ms.
Pełny tekst źródłaZheng, Ye, Jaime A. Martinez-Acosta, Mohammed Khimji, Luiz C. A. Barbosa, Guy J. Clarkson i Martin Wills. "Asymmetric Transfer Hydrogenation of Aryl Heteroaryl Ketones and o-Hydroxyphenyl Ketones Using Noyori-Ikariya Catalysts". W ECSOC-25. Basel Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11774.
Pełny tekst źródłaTsai, S., i S. Que Hee. "98. Validation of a Passive Sampler for Ketones". W AIHce 1999. AIHA, 1999. http://dx.doi.org/10.3320/1.2763419.
Pełny tekst źródłaDurnin, S., C. Blackburn, E. Ryan, E. Dobos, B. Conway, SM O’Donnell, S. Walsh i MJ Barrett. "G297(P) The utility of ketones at triage". W Royal College of Paediatrics and Child Health, Abstracts of the Annual Conference, 24–26 May 2017, ICC, Birmingham. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2017. http://dx.doi.org/10.1136/archdischild-2017-313087.290.
Pełny tekst źródłaRamasami, Ponnadurai, Naziah Jaufeerally i Hassan Abdallah. "Theoretical Insights into Novel Telluro-ketones". W The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01088.
Pełny tekst źródłaSolovyev, Pavel, Anastasia Fesenko, Ekaterina Dem'yachenko i Anatoly Shutalev. "A novel selective synthesis of β-isothiocyanato ketones". W The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a017.
Pełny tekst źródłaRamasami, Ponnadurai, i Naziah Jaufeerally. "Structures, Energetics and Stabilities of Novel Telluro-Ketones". W The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-e023.
Pełny tekst źródłaTsoi, Valerie, i M. Sanz. "WATER BINDING TO KETONES: CYCLOOCTANONE···(H2O)3−7 COMPLEXES". W 2023 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2023. http://dx.doi.org/10.15278/isms.2023.6947.
Pełny tekst źródłaSiewert, Inke. "Electroreduction of C=O Bonds in CO2, Ketones, and Aldehydes". W MATSUS23 & Sustainable Technology Forum València (STECH23). València: FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2022. http://dx.doi.org/10.29363/nanoge.matsus.2023.032.
Pełny tekst źródłaRaporty organizacyjne na temat "Ketones"
Kallupalayam Ramasamy, Karthikeyan, Mond Guo, Udishnu Sanyal i Laura CA Meyer. Mixed Oxygenate Conversion to Sustainable Aviation Fuel via Ketones Intermediate. Office of Scientific and Technical Information (OSTI), wrzesień 2023. http://dx.doi.org/10.2172/2332864.
Pełny tekst źródłaBrown, H. C., K. Ganesan i R. K. Dhar. Enolboration. 4. An Examination of the Effect of the Leaving Group (X) on the Stereoselective Enolboration of Ketones with Various R2BX/Et3N. New Reagents for the Selective Generation of either Z or E Enol Borinates from Representative Ketones. Fort Belvoir, VA: Defense Technical Information Center, listopad 1992. http://dx.doi.org/10.21236/ada257829.
Pełny tekst źródłaSuri, Suresh C., i Jacob C. Marcischak. New Application of Bromotrimethylsilane: Elaboration of Aldehydes/Ketones into Homologous Alpha-Beta-Unsaturated Esters via Beta-Hydroxy Esters. Fort Belvoir, VA: Defense Technical Information Center, styczeń 2003. http://dx.doi.org/10.21236/ada410496.
Pełny tekst źródłaBrown, H. C., K. Ganesan i R. K. Dhar. Enolboration 3. An Examination of the Effect of Variable Steric Requirements of R on the Stereoselective Enolboration of Ketones with R2BCl/Et3N. Bis(Bicyclo(2.2.2)Octyl)Chloroborane/Triethylamine - A New Reagent Which Achieves the Selective Generation of E Enolborinates from Representative Ketones. Fort Belvoir, VA: Defense Technical Information Center, kwiecień 1992. http://dx.doi.org/10.21236/ada250066.
Pełny tekst źródłaBrown, Herbert C., Raj K. Dhar, Raman K. Bakshi, Paul K. Pandiarajan i Bakthan Singaram. Major Effect of the Leaving Group in Dialkylboron Chlorides and Triflates in Controlling the Stereospecific Conversion of Ketones into Either (E)- or (Z)- Enol Borinatesxxb. Fort Belvoir, VA: Defense Technical Information Center, marzec 1989. http://dx.doi.org/10.21236/ada209988.
Pełny tekst źródłaBrownJason Fuentes, Raymond. Study of Poly(ether ketone ketone) (PEKK): Outgassing Characteristics and Likely Residual Synthesis Impurities. Office of Scientific and Technical Information (OSTI), lipiec 2020. http://dx.doi.org/10.2172/1643746.
Pełny tekst źródłaBrown, H. C., P. V. Ramachandran, S. A. Weissman i S. Swaminathan. Selective Reductions. 46. Effect of the Steric Requirement at the 2- Position of Apopinene on Chiral Reductions. B-Iso-2-n-Propylapopinocampheyl-9- Borabicyclo(3.3.1)Nonane as Improved Reagents for the Chiral Reduction of Alpha, Beta-Acetylenic Ketones and Alpha-Keto Esters. Fort Belvoir, VA: Defense Technical Information Center, styczeń 1991. http://dx.doi.org/10.21236/ada230919.
Pełny tekst źródłaLiu, Qiong. Ketone Body Metabolic Enzyme OXCT1 Regulates Prostate Cancer Chemoresistance. Fort Belvoir, VA: Defense Technical Information Center, październik 2014. http://dx.doi.org/10.21236/ada613410.
Pełny tekst źródłaFrazier, J. L. Damage tolerance evaluation of PEEK (polyether ether ketone) composites: Final report. Office of Scientific and Technical Information (OSTI), grudzień 1988. http://dx.doi.org/10.2172/6617723.
Pełny tekst źródłaMast, T. J., J. A. Dill, J. J. Evanoff, R. L. Rommereim, R. J. Weigel i R. B. Westerberg. Inhalation developmental toxicology studies: Teratology study of methyl ethyl ketone in mice: Final report. Office of Scientific and Technical Information (OSTI), luty 1989. http://dx.doi.org/10.2172/6277861.
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