Добірка наукової літератури з теми "Total Synthesis, Methodology"
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Статті в журналах з теми "Total Synthesis, Methodology"
Petrovčič, Jan, Chad Nicholas Ungarean, and David Sarlah. "Recent Chemical Methodology Advances in the Total Synthesis of Meroterpenoids." Acta Chimica Slovenica 68, no. 2 (June 15, 2021): 247–67. http://dx.doi.org/10.17344/acsi.2021.6921.
Повний текст джерелаIsobe, Minoru, and Akinari Hamajima. "Ciguatoxin: developing the methodology for total synthesis." Natural Product Reports 27, no. 8 (2010): 1204. http://dx.doi.org/10.1039/b919467n.
Повний текст джерелаUmezawa, Taiki, and Fuyuhiko Matsuda. "Recent progress toward synthesis of chlorosulfolipids: total synthesis and methodology." Tetrahedron Letters 55, no. 19 (May 2014): 3003–12. http://dx.doi.org/10.1016/j.tetlet.2014.03.082.
Повний текст джерелаWilliams, Craig, and Rebecca Pouwer. "Method in the Madness - Methodology from Total Synthesis." Synlett 23, no. 10 (May 29, 2012): 1446–58. http://dx.doi.org/10.1055/s-0031-1290967.
Повний текст джерелаVedejs, Edwin, and Chutima Kongkittingam. "A Total Synthesis of (−)-Hemiasterlin UsingN-Bts Methodology." Journal of Organic Chemistry 66, no. 22 (November 2001): 7355–64. http://dx.doi.org/10.1021/jo0104882.
Повний текст джерелаKeck, Gary E., Eugene P. Boden, and Michael R. Wiley. "Total synthesis of (+)-colletodiol: new methodology for the synthesis of macrolactones." Journal of Organic Chemistry 54, no. 4 (February 1989): 896–906. http://dx.doi.org/10.1021/jo00265a033.
Повний текст джерелаUmezawa, Taiki, and Fuyuhiko Matsuda. "ChemInform Abstract: Recent Progress Toward Synthesis of Chlorosulfolipids: Total Synthesis and Methodology." ChemInform 45, no. 29 (July 3, 2014): no. http://dx.doi.org/10.1002/chin.201429265.
Повний текст джерелаYeung, Kay, Rory C. Mykura, and Varinder K. Aggarwal. "Lithiation–borylation methodology in the total synthesis of natural products." Nature Synthesis 1, no. 2 (February 2022): 117–26. http://dx.doi.org/10.1038/s44160-021-00012-1.
Повний текст джерелаXiang, Alan X., Donald A. Watson, Taotao Ling, and Emmanuel A. Theodorakis. "Total Synthesis of Clerocidin via a Novel, Enantioselective Homoallenylboration Methodology." Journal of Organic Chemistry 63, no. 20 (October 1998): 6774–75. http://dx.doi.org/10.1021/jo981331l.
Повний текст джерелаJohnstone, Craig, William J. Kerr, and Udo Lange. "Total synthesis of (+)-taylorione utilising modified Pauson–Khand reaction methodology." J. Chem. Soc., Chem. Commun., no. 4 (1995): 457–58. http://dx.doi.org/10.1039/c39950000457.
Повний текст джерелаДисертації з теми "Total Synthesis, Methodology"
O'Hora, Paul. "Novel methodology towards the total synthesis of Pseudopterogorgia metabolites." Thesis, Loughborough University, 2013. https://dspace.lboro.ac.uk/2134/13437.
Повний текст джерелаVarela, Ann. "Application of lithiantion-borylation methodology to alkaloid synthesis : total synthesis of (-) -stemaphylline." Thesis, University of Bristol, 2017. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.730870.
Повний текст джерелаGerstenberger, Brian Stephen. "Progress towards the total synthesis of diazonamide A and related new methodology /." Diss., Digital Dissertations Database. Restricted to UC campuses, 2007. http://uclibs.org/PID/11984.
Повний текст джерелаStevens, Kiri. "Methodology for the synthesis of NP25302 and other bioactive natural products." Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:ae18879e-d75e-4280-ba55-1ae08e64034f.
Повний текст джерелаMarshall, Laura. "Novel methodology for the synthesis of ¹³C-labelled phenols and its application to the total synthesis of polyphenols /." St Andrews, 2010. http://hdl.handle.net/10023/875.
Повний текст джерелаMarshall, Laura J. "Novel methodology for the synthesis of ¹³C-Labelled phenols and its application to the total synthesis of polyphenols." Thesis, University of St Andrews, 2010. http://hdl.handle.net/10023/875.
Повний текст джерелаPicot, Ondine. "Homoallylation énantiosélective d'aldéhydes par des diènes 1,3. Vers la synthèse de la (-)-spongidepsine." Thesis, Université Paris sciences et lettres, 2020. http://www.theses.fr/2020UPSLS030.
Повний текст джерела-)-Spongidepsin is a cyclodepsipeptide isolated from the marine sponge Spongia sp. This compound exhibitscytotoxic and antiproliferative activities against several cancer cell lines. Until now, five total syntheses and two formal ones have already been reported, all of them including a disconnection of (-)-spongidepsin into three fragments: a carboxylic acid (C1-C5), a bis-homoallylic alcohol (C6-C13) and N-methyl-phenylalanine. Our objective was to develop a flexible, short and scalable synthesis of (-)-spongidepsin that could be used for further biological studies and for the preparation of analogs. The synthesis of the acid fragment was achieved according to reported procedure. To access the C6-C13 fragment, an unprecedented enantioselective nickel-catalyzed homoallylation of aldehydes with dienes was developed. The reaction was performed using a combination of NiCl2 with enantio enriched phosphoramidites derived from BINOL in the presence of a hydrogen donor, Et2Zn and a 1,3-diene. A range of aromatic, aliphatic and α,β-unsaturated aldehydes were transformed into the corresponding bis-homoallylic alcohols with moderate to good yields and enantioselectivity. The method was successfully applied to the synthesis of C6-C13 fragment of (-)-spongidepsin
Lewis, Simon Eliot. "The decarboxylative Ireland-Claisen rearrangement : methodology studies and approaches to the total synthesis of (-)-suaveoline." Thesis, Imperial College London, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.429457.
Повний текст джерелаRosset, Isac George. "Diazocetonas α,β-insaturadas como reagentes multifuncionais: aplicação na síntese de alcaloides piperidínicos e pirrolidínicos." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/75/75133/tde-20052015-101409/.
Повний текст джерелаThe first part of this work describes the preparation of a new HWE olefination reagent to prepare diazoketones α, β-unsaturated with Z geometry and its application in the synthesis of functionalized piperidine cores. After the optimization of the HWE reaction using benzaldehyde as a standard it was possible to prepare the desired Z isomer in 92% (Z:E 9:1). The key reaction for formation of the piperidine cores, N-H metal-catalyzed insertion performed to give a yield of up to 70%. The versatility of the methodology was demonstrated by an application to the synthesis of the natural product (±)-3,4,5-triidroxypiperidine and studies in the synthesis of (-)-1-deoxy-altronojirimicine. The chemistry of α, β-unsaturated diazoketones was also employed in the synthesis of another natural product, the alkaloid (±)-preussine. The employed route showed high stereoselectivity in the key-reaction (Stevens Rearrangement) as well as in the subsequent reduction of the formed ketone with a reducing agent (L-Selectride) giving an overall yield of 40%. We also tried to extend the methodology to prepare trisubstituted α, β-unsaturated diazoketones from the reaction with the olefination reagent and ketones. However, after several attempts no fruitful results were abtained.
Throup, Adam Eric. "Synthetic methodology and application of enamine [2+2] cyclisations for cyclobutane synthesis : development of integrin antagonists as anticancer therapeutics towards a total synthesis of providencin." Thesis, University of Bradford, 2015. http://hdl.handle.net/10454/14411.
Повний текст джерелаКниги з теми "Total Synthesis, Methodology"
Skiba, Grzegorz. Fizjologiczne, żywieniowe i genetyczne uwarunkowania właściwości kości rosnących świń. The Kielanowski Institute of Animal Physiology and Nutrition, Polish Academy of Sciences, 2020. http://dx.doi.org/10.22358/mono_gs_2020.
Повний текст джерелаЧастини книг з теми "Total Synthesis, Methodology"
Wang, Qian, Jie-Ping Zhu, Kyriacos C. Nicolaou, Henry N. C. Wong, and Wei-Dong Li. "Total Synthesis of Natural Products and the Synergy with Synthetic Methodology." In Organic Chemistry - Breakthroughs and Perspectives, 33–79. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527664801.ch2.
Повний текст джерелаBansal, Paramjit S., and Paul F. Alewood. "Total Chemical Synthesis of κ-Casein Using Native Ligation Methodology." In Peptides: The Wave of the Future, 115–16. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-0464-0_51.
Повний текст джерелаRomo, D., R. M. Rzasa, W. D. Schmitz, J. Yang, S. T. Cohn, L. R. Buchler, H. A. Shea, et al. "Total Synthesis of Marine Natural Products Driven by Novel Structure, Potent Biological Activity, and/or Synthetic Methodology." In The Role of Natural Products in Drug Discovery, 103–48. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-662-04042-3_4.
Повний текст джерелаGrossman, Robert B., and Ravindra M. Rasne. "Methodology Validation and Structure Correction by Total Synthesis: The Case of the Clerodane Diterpenoid, Sacacarin." In Strategies and Tactics in Organic Synthesis, 1–18. Elsevier, 2004. http://dx.doi.org/10.1016/s1874-6004(04)80005-4.
Повний текст джерелаSheshukov, Oleg, and Michael Mikheenkov. "Peculiarities of Portland Cement Clinker Synthesis in the Presence of a Significant Amount of SO3 in a Raw Mix." In Cement Industry - Optimization, Characterization and Sustainable Application. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.94915.
Повний текст джерелаPyrgakis, Konstantinos A., and Antonis C. Kokossis. "A New Methodology to Apply Total Site Analysis as a Synthesis Tool to Select and Integrate Processes in Multiple-Product Biorefinery Plants." In Computer Aided Chemical Engineering, 2073–78. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-444-63428-3.50350-7.
Повний текст джерелаBurko, Kateryna. "SCOPE OF APPLICATION OF MANAGEMENT ACCOUNTING TOOLS FOR THE NEEDS OF MANAGEMENT OF THE BEEKEEPING INDUSTRY." In Traditional and innovative approaches to scientific research: theory, methodology, practice. Publishing House “Baltija Publishing”, 2022. http://dx.doi.org/10.30525/978-9934-26-241-8-23.
Повний текст джерелаV. Yemelyanov, Vladislav, Roman K. Puzanskiy, Mikhail S. Burlakovskiy, Lyudmila A. Lutova, and Maria F. Shishova. "Metabolic Profiling of Transgenic Tobacco Plants Synthesizing Bovine Interferon-Gamma." In Metabolomics - Methodology and Applications in Medical Sciences and Life Sciences. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96862.
Повний текст джерелаGuaita Martinez, Jose Manuel, José María Martín Martín, and José Antonio Salinas Fernández. "Innovation in the Measurement of Tourism Competitiveness." In Advances in Business Strategy and Competitive Advantage, 268–88. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-1169-5.ch013.
Повний текст джерелаLipin, Mykola, and Nataliia Husieva. "THE PRODUCTIVITY OF ORDER AND CHAOS IN THE METAMORPHOSIS OF CREATIVITY." In Science, technology, and innovation: the experience of European countries and prospects for Ukraine. Publishing House “Baltija Publishing”, 2021. http://dx.doi.org/10.30525/978-9934-26-190-9-10.
Повний текст джерелаТези доповідей конференцій з теми "Total Synthesis, Methodology"
Toffolo, Andrea. "Multi-Objective Synthesis Optimization of Heat Exchanger Networks With Arbitrary Topology." In ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-68651.
Повний текст джерелаGeorgopoulos, Nikolaos G., Michael R. von Spakovsky, and J. Ricardo Mun˜oz. "A Decomposition Strategy Based on Thermoeconomic Isolation Applied to the Optimal Synthesis/Design and Operation of a Fuel Cell Based Total Energy System." In ASME 2002 International Mechanical Engineering Congress and Exposition. ASMEDC, 2002. http://dx.doi.org/10.1115/imece2002-33320.
Повний текст джерелаFillingim, Kenton B., Richard Ossie Nwaeri, Felipe Borja, Katherine Fu, and Christiaan J. J. Paredis. "Design Heuristics: Analysis and Synthesis From Jet Propulsion Laboratory’s Architecture Team." In ASME 2018 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/detc2018-85584.
Повний текст джерелаLaw-Kam Cio, Yann-Seing, Yuanchao Ma, Aurelian Vadean, Giovanni Beltrame, and Sofiane Achiche. "Objective Reduction Using Axiomatic Design and Product-Related Dependencies: A Layout Synthesis of an Autonomous Greenhouse Case Study." In ASME 2020 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/detc2020-22397.
Повний текст джерелаOyarza´bal, Borja, Michael R. von Spokovsky, Michael W. Ellis, J. Ricardo Mun˜oz, and Nikolaos G. Georgopoulos. "Application of a Decomposition Strategy to the Optimal Synthesis/Design of a Fuel Cell Sub-System." In ASME 2002 International Mechanical Engineering Congress and Exposition. ASMEDC, 2002. http://dx.doi.org/10.1115/imece2002-33317.
Повний текст джерелаAlves, Anabela C., Francisco Moreira, Celina P. Leão, and Sandra Fernandes. "Ten Years of Positive Feedback on Project-Based Learning From First-Year Engineering Students’ Perspective." In ASME 2020 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/imece2020-23212.
Повний текст джерелаAlba, Antonio, Francesco Bucchi, Francesco Frendo, and Marco Gabiccini. "Kinematic Optimization of the Arm of a Working Machine." In ASME 2014 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/detc2014-34885.
Повний текст джерелаRancruel, Diego F., and Michael R. von Spakovsky. "A Decomposition Strategy Applied to the Optimal Synthesis/Design and Operation of an Advanced Fighter Aircraft System: A Comparison With and Without Airframe Degrees of Freedom." In ASME 2003 International Mechanical Engineering Congress and Exposition. ASMEDC, 2003. http://dx.doi.org/10.1115/imece2003-55402.
Повний текст джерелаBerghe, Nadejda. "Administration of fiscal revenues by the customs service of the Republic of Moldova." In 26th International Scientific Conference “Competitiveness and Innovation in the Knowledge Economy". Academy of Economic Studies of Moldova, 2023. http://dx.doi.org/10.53486/cike2022.42.
Повний текст джерелаRovenko, Elena. "ERWIN PANOFSKY�S ICONOLOGY AND THE ANALYSIS OF MUSICAL COMPOSITION: ON SEARCHING NEW SEMANTIC STRATEGIES." In 9th SWS International Scientific Conferences on ART and HUMANITIES - ISCAH 2022. SGEM WORLD SCIENCE, 2022. http://dx.doi.org/10.35603/sws.iscah.2022/s08.08.
Повний текст джерелаЗвіти організацій з теми "Total Synthesis, Methodology"
Blumwald, Eduardo, and Avi Sadka. Sugar and Acid Homeostasis in Citrus Fruit. United States Department of Agriculture, January 2012. http://dx.doi.org/10.32747/2012.7697109.bard.
Повний текст джерелаTorres, Marissa, and Norberto Nadal-Caraballo. Rapid tidal reconstruction with UTide and the ADCIRC tidal database. Engineer Research and Development Center (U.S.), August 2021. http://dx.doi.org/10.21079/11681/41503.
Повний текст джерелаMelnyk, Olesia. MEDIA DISCOURSE AROUND THE FIGURE OF ORIANA FALLACHI AND HER JOURNALISM DURING 2017–2020. Ivan Franko National University of Lviv, March 2021. http://dx.doi.org/10.30970/vjo.2021.50.11114.
Повний текст джерела