Добірка наукової літератури з теми "Versatile intermediates"
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Статті в журналах з теми "Versatile intermediates"
Boeske, Juergen, Edgar Niecke, Edgar Ocando-Mavarez, Jean Pierre Majoral, and Guy Bertrand. "Phosphonitriles: versatile intermediates." Inorganic Chemistry 25, no. 16 (July 1986): 2695–98. http://dx.doi.org/10.1021/ic00236a008.
Повний текст джерелаBelletire, J. L. "Acylcyanamides: Versatile Synthetic Intermediates." Synthetic Communications 18, no. 16-17 (November 1988): 2063–71. http://dx.doi.org/10.1080/00397918808068275.
Повний текст джерелаR. Katritzky, Alan, Adam S. Vincek, and Peter J. Steel. "Triphenylphosphoranylidene Substituted Heterocycles as Versatile Intermediates." HETEROCYCLES 76, no. 2 (2008): 1401. http://dx.doi.org/10.3987/com-08-s(f)12.
Повний текст джерелаBritten, Thomas K., Paul D. Kemmitt, Nathan R. Halcovitch, and Susannah C. Coote. "1,2-Dihydropyridazines as Versatile Synthetic Intermediates." Synlett 31, no. 05 (February 13, 2020): 459–62. http://dx.doi.org/10.1055/s-0039-1690825.
Повний текст джерелаBari, Ahmed. "Monosaccharidic Push-pull Butadienes: Versatile Synthetic Intermediates." Zeitschrift für Naturforschung B 69, no. 1 (January 1, 2014): 98–102. http://dx.doi.org/10.5560/znb.2014-3179.
Повний текст джерелаAttanasi, Orazio A., and Luciano Caglioti. "CONJUGATED AZOALKENES: ATTRACTIVE PRODUCTS AND VERSATILE INTERMEDIATES." Organic Preparations and Procedures International 18, no. 5 (October 1986): 299–327. http://dx.doi.org/10.1080/00304948609356836.
Повний текст джерелаFlashman, Emily, and Christopher J. Schofield. "The most versatile of all reactive intermediates?" Nature Chemical Biology 3, no. 2 (February 2007): 86–87. http://dx.doi.org/10.1038/nchembio0207-86.
Повний текст джерелаZellner, Armin, and Manfred Schlosser. "Pentadienyltitaniums as Versatile Intermediates: Regio- and Stereoselectivities." Synlett 2001, Special Issue (2001): 1016–18. http://dx.doi.org/10.1055/s-2001-14650.
Повний текст джерелаBarrett, Anthony G. M., and Gregory G. Graboski. "Conjugated nitroalkenes: versatile intermediates in organic synthesis." Chemical Reviews 86, no. 5 (October 1986): 751–62. http://dx.doi.org/10.1021/cr00075a002.
Повний текст джерелаMichael, J. P., C. B. de Koning, D. Gravestock, G. D. Hosken, A. S. Howard, C. M. Jungmann, R. W. M. Krause, A. S. Parsons, S. C. Pelly, and T. V. Stanbury. "Enaminones: versatile intermediates for natural product synthesis." Pure and Applied Chemistry 71, no. 6 (June 30, 1999): 979–88. http://dx.doi.org/10.1351/pac199971060979.
Повний текст джерелаДисертації з теми "Versatile intermediates"
Vincent-Rocan, Jean-François. "N-Isocyanates : Versatile Intermediates in Heterocyclic Synthesis." Thesis, Université d'Ottawa / University of Ottawa, 2016. http://hdl.handle.net/10393/34864.
Повний текст джерелаOsborn, Helen M. I. "Activated aziridines as versatile intermediates organic synthesis." Thesis, University of Bristol, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238927.
Повний текст джерелаSwindlehurst, Marianne. "Ethoxyvinylarenes as versatile intermediates for heterocycle synthesis." Thesis, University of Surrey, 2017. http://epubs.surrey.ac.uk/841208/.
Повний текст джерелаHadden, Mark. "Enamides and enaminones : versatile intermediates for heterocycle formation." Thesis, Queen's University Belfast, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.322956.
Повний текст джерелаMcIntyre, Peter Brian Alexander. "Chemoenzymatic oxidation of arenes : versatile intermediates for organic synthesis." Thesis, Queen's University Belfast, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.602501.
Повний текст джерелаMcCreanor, Niall G. "Rhodacyclopentanones as versatile catalytic intermediates for the synthesis of complex scaffolds." Thesis, University of Bristol, 2016. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.702463.
Повний текст джерелаDa, Cruz Ana Filipa P. "C-branched carbohydrate lactones : versatile intermediates in the synthesis of branched iminosugars." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.670024.
Повний текст джерелаBower, John F. "Cyclic sulfamidates as versatile intermediates for N-heterocycle construction : applications in total synthesis." Thesis, University of Bristol, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.439953.
Повний текст джерелаFilipa, P. da Cruz Ana. "C-branched carbohydrate lactones : Versatile intermediatesin the synthesis of branched bioactive." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509913.
Повний текст джерелаChien, Ting-Lin, and 簡廷燐. "Tricarbonyliron Triene Complexes As Versatile Synthetic Intermediate." Thesis, 1995. http://ndltd.ncl.edu.tw/handle/29201121273100930729.
Повний текст джерела國立中山大學
化學學系
83
Organoiron complexes are readily available and can serve as starting meterials for the synthesis of numerous natural products. The synthetic applications of the tricarbonyliron triene complexes not been explored previously. The organic compound, 1-methylene-4-methoxycyclohex-2,4- diene, does not exist which will tautomerized rapidly to 4-methylanisole. The Fe(CO)3 act as a protecting and stabilizing group for the exocyclic methylene group and this has important synthetic applications. We now proposed to carry out new chemical and stereochemistry applications of a new series of organoiron complex. (1) Electrophilic substitution reaction , including trapping with nucleophiles. (2) 1,3-Dipolar cycloaddition reactions.
Частини книг з теми "Versatile intermediates"
Keglevich, György. "Phosphinine Derivatives and their Use as Versatile Intermediates in P-Heterocyclic Chemistry." In Topics in Heterocyclic Chemistry, 65–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/7081_2008_8.
Повний текст джерелаFustero, Santos, Juan F. Sanz-Cervera, Julio Piera, María Sánchez-Roselló, Diego Jiménez, and Gema Chiva. "Fluorinated β-Enamino Esters as Versatile Synthetic Intermediates: Synthesis of Fluorinated β-Amino Acids and Uracils." In ACS Symposium Series, 593–610. Washington, DC: American Chemical Society, 2005. http://dx.doi.org/10.1021/bk-2005-0911.ch034.
Повний текст джерелаYamamoto, Hiroshi, Tadashi Hanaya, Kiyoshi Torigoe, and Wolfgang Pfleiderer. "N 2-(N,N-Dimethylaminomethylene)-O 4-(2-p-Nitrophenyl. Ethyl)-Biopterin: A Versatile Intermediate for a Glycosidation Reaction." In Advances in Experimental Medicine and Biology, 21–24. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2960-6_3.
Повний текст джерелаTurnbull, Kenneth, and Andrew J. Weisner. "o-Alkynylsydnones as Versatile Intermediates for Heterocyclic Synthesis." In 19th International Congress on Heterocyclic Chemistry, 348. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50340-3.
Повний текст джерелаD. Adesina, Adebimpe. "The Chemistry of Benzo and Carbocyclic Derivatives of Pyridine." In Exploring Chemistry with Pyridine Derivatives [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.108127.
Повний текст джерелаHou, Z. W., and H. C. Xu. "7 Electrochemically Generated Nitrogen-Centered Radicals." In Electrochemistry in Organic Synthesis. Stuttgart: Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/sos-sd-236-00136.
Повний текст джерелаZhang, J., D. Liu, and Y. Chen. "1.9 Oxygen-Centered Radicals." In Free Radicals: Fundamentals and Applications in Organic Synthesis 1. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-234-00177.
Повний текст джерелаKaga, A., and H. Yorimitsu. "1.6 Sulfur-, Selenium-, and Silicon-Centered Radicals." In Free Radicals: Fundamentals and Applications in Organic Synthesis 1. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-234-00090.
Повний текст джерелаMalhotra, Deepika, Joyeeta Mukherjee, and Munishwar N. Gupta. "Sustainability of Biocatalytic Processes." In Chemical Processes for a Sustainable Future, 388–421. The Royal Society of Chemistry, 2014. http://dx.doi.org/10.1039/bk9781849739757-00388.
Повний текст джерелаTaber, Douglass. "Enantioselective Synthesis of Alcohols and Amines." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0036.
Повний текст джерелаТези доповідей конференцій з теми "Versatile intermediates"
Lin, Y. C., W. S. Wang, T. Gessner, and M. Esashi. "Nanoporous gold as a versatile bonding intermediate." In 2014 4th IEEE International Workshop on Low Temperature Bonding for 3D Integration (LTB-3D). IEEE, 2014. http://dx.doi.org/10.1109/ltb-3d.2014.6886185.
Повний текст джерелаMoreira, Bárbara V., and Cristiano Raminelli. "Synthesis of 3-hydroxy-2-(trimethylsilyl)phenyl trifluoromethanesulfonate as a versatile intermediate in preparative organic chemistry." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201391593549.
Повний текст джерелаGoujot, Daniel, Têko Gouyo, Philippe Bohuon, and Francis Courtois. "A versatile simulator for defrosting, convective and boiling drying during hot air frying process." In the 7th International Food Operations and Processing Simulation Workshop. CAL-TEK srl, 2021. http://dx.doi.org/10.46354/i3m.2021.foodops.003.
Повний текст джерелаHolmes, Jeffrey W., and Thomas K. Borg. "Isotonic Biaxial Loading: An Economic, Versatile Method for the Study of Fibroblast-Populated Collagen Gels." In ASME 1999 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1999. http://dx.doi.org/10.1115/imece1999-0402.
Повний текст джерелаParaschis, L., M. C. Bashaw, A. Liu, and L. Hesselink. "Properties of Resonant Two-Photon Processes in Photorefractive Media." In Adaptive Optics. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/adop.1996.jtud.4.
Повний текст джерелаRoßmann, Ju¨rgen, Michael Schluse, and Thomas Jung. "Introducing Intuitive and Versatile Multi Modal Graphical Programming Means to Enhance Virtual Environments." In ASME 2008 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2008. http://dx.doi.org/10.1115/detc2008-49517.
Повний текст джерелаHosmane, Ramachandra, Saika Siddiqui, and Bruce Gustafson. "A New Synthetic Approach toward Ring-Expanded ("Fat") Purine Nucleobases: Synthesis and Use of 5-Dichloromethyl-1-p-methoxybenzyl-4-nitroimidazole as a Versatile Intermediate." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01740.
Повний текст джерелаMichlik, P., and O. Racek. "XFEM Modeling of Effective Thermal Properties and Fracture of Thermal Barrier Coatings." In ITSC2005, edited by E. Lugscheider. Verlag für Schweißen und verwandte Verfahren DVS-Verlag GmbH, 2005. http://dx.doi.org/10.31399/asm.cp.itsc2005p0293.
Повний текст джерелаPotter, B. G., and J. H. Simmons. "Quantum-confinement effects in rf-magnetron sputtered CdTe:glass composite thin films." In OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.wo4.
Повний текст джерелаPetersen, Thomas, Qian Wu, Nanjun Liu, Brian J. O’Donnell, Gene Korn, Parker Hewitt, and Changjun Zhou. "Compressible Carbon: Particle Behavior in Drilling Fluids and Field-Scale Deployment." In Offshore Technology Conference. OTC, 2022. http://dx.doi.org/10.4043/31767-ms.
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