Gotowa bibliografia na temat „Cuprate addition”
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Artykuły w czasopismach na temat "Cuprate addition"
Snyder, James P. "Mechanism of Lithium Cuprate Conjugate Addition: Neutral Tetracoordinate CuI Cuprates as Essential Intermediates". Journal of the American Chemical Society 117, nr 44 (listopad 1995): 11025–26. http://dx.doi.org/10.1021/ja00149a033.
Pełny tekst źródłaLi, W. M., J. F. Zhao, L. P. Cao, Z. Hu, Q. Z. Huang, X. C. Wang, Y. Liu i in. "Superconductivity in a unique type of copper oxide". Proceedings of the National Academy of Sciences 116, nr 25 (20.05.2019): 12156–60. http://dx.doi.org/10.1073/pnas.1900908116.
Pełny tekst źródłaBreit, Bernhard. "ortho-Diphenylphosphanylbenzoyl-Directed Cuprate Addition to Acyclic Enoates". Angewandte Chemie International Edition 37, nr 4 (2.03.1998): 525–27. http://dx.doi.org/10.1002/(sici)1521-3773(19980302)37:4<525::aid-anie525>3.0.co;2-m.
Pełny tekst źródłaWang, Qisi, Karin von Arx, Masafumi Horio, Deepak John Mukkattukavil, Julia Küspert, Yasmine Sassa, Thorsten Schmitt i in. "Charge order lock-in by electron-phonon coupling in La1.675Eu0.2Sr0.125CuO4". Science Advances 7, nr 27 (czerwiec 2021): eabg7394. http://dx.doi.org/10.1126/sciadv.abg7394.
Pełny tekst źródłaClive, Derrick L. J., Chengzhi Zhang, Yuanxi Zhou i Yong Tao. "Addition of dimethylphenylsilyl cuprates to vinyl epoxides: Effect of cuprate stoichiometry on stereochemistry and refiochemistry". Journal of Organometallic Chemistry 489, nr 1-2 (marzec 1995): C35—C37. http://dx.doi.org/10.1016/0022-328x(94)05224-y.
Pełny tekst źródłaAgterberg, Daniel F., J. C. Séamus Davis, Stephen D. Edkins, Eduardo Fradkin, Dale J. Van Harlingen, Steven A. Kivelson, Patrick A. Lee, Leo Radzihovsky, John M. Tranquada i Yuxuan Wang. "The Physics of Pair-Density Waves: Cuprate Superconductors and Beyond". Annual Review of Condensed Matter Physics 11, nr 1 (10.03.2020): 231–70. http://dx.doi.org/10.1146/annurev-conmatphys-031119-050711.
Pełny tekst źródłaHutchinson, D. K., S. A. Hardinger i P. L. Fuchs. "Amine-directed addition of cuprate reagents to cyclopentenyl sulfones". Tetrahedron Letters 27, nr 13 (styczeń 1986): 1425–28. http://dx.doi.org/10.1016/s0040-4039(00)84276-8.
Pełny tekst źródłaMulzer, Johann, Gerd Dürner i Dirk Trauner. "Formal Total Synthesis of(—)-Morphine by Cuprate Conjugate Addition". Angewandte Chemie International Edition in English 35, nr 2324 (grudzień 1996): 2830–32. http://dx.doi.org/10.1002/anie.199628301.
Pełny tekst źródłaLv, Bo, i Wei Guo. "The spin pairing symmetry of d-wave superconductor indicated by tunneling spectroscopy". International Journal of Modern Physics B 31, nr 25 (10.10.2017): 1745017. http://dx.doi.org/10.1142/s0217979217450175.
Pełny tekst źródłaSalas, P., M. A. Solís, M. Fortes i F. J. Sevilla. "Thermodynamic properties of underdoped YBa2Cu3O6+x cuprates for several doping values". International Journal of Modern Physics B 31, nr 13 (23.02.2017): 1750100. http://dx.doi.org/10.1142/s0217979217501004.
Pełny tekst źródłaRozprawy doktorskie na temat "Cuprate addition"
Kasprzyk, Milena, i milena kasprzyk@freehills com. "Synthetic Studies Towards the Tridachione Family of Marine Natural Products". Flinders University. Chemistry, Physics and Earth Sciences, 2008. http://catalogue.flinders.edu.au./local/adt/public/adt-SFU20081107.085933.
Pełny tekst źródłaO'Connor, Brian 1961. "Studies towards the synthesis of the novel antileukemic agent CI-920 and the addition of cuprates to vinyltriphenylphosphonium bromide : a synthesis of 1,5-disubstituted 1Z,4Z-pentadienes". Thesis, McGill University, 1987. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=75443.
Pełny tekst źródłaCunha, Rodrigo Luiz Oliveira Rodrigues. "Novos aspectos e aplicações da química de teluranas e de teluretos orgânicos". Universidade de São Paulo, 2005. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-27082008-073450/.
Pełny tekst źródłaThe first part of this thesis deals with the study of the reactivity of electrophilic tellurium compounds, mainly tellurium tetrachloride and aromatic tellurium trichlorides. New aspects of the reactivity of TeCl4 towards alkynes and some acetophenones were disclosed. A mechanistic rationale for each of the processes studied was possible by the determination of the stereochemistry for each product by monocrystal X-ray diffraction analysis. The proposition of the formation of cationic intermediates in the addition reaction of TeCl4 to alkynes was corroborated by the detection and characterization of transient intermediates by ESI-MS/MS experiments. Besides the new aspects of the Tellurium chemistry found, the prepared compounds showed a high and selective activity as inhibitors of cysteine proteases. A pair of enantiomers of a tellurane showed different activities against Human Catepsin B due to a stereochemical dependence in the enzyme/inhibitor interaction. The second part of the present work deals with the development of the ring opening reaction of aziridines by organometallic reagents of copper prepared from vinylic and arylic tellurides. These reactions led to homoallylic and homobenzylic amine derivatives. Finally, the reactivity of 2-alkenyl aziridines was studied towards a series of organometallic reagents of lithium, magnesium, copper and zinc which biased the regio- and stereoselectivities of the ring opening reactions.
Ma, Jianguo. "Acyclic stereocontrol and chemical diversity & application to the total synthesis of Bafilomycin A₁". Thèse, 2001. http://hdl.handle.net/1866/14335.
Pełny tekst źródłaCérat, Pascal. "Synthèse et utilisation de dérivés de cyclopropane-1,1-diesters énantioenrichis vers l'obtention d'allènes hautement substitués". Thèse, 2011. http://hdl.handle.net/1866/6296.
Pełny tekst źródłaThe subject of this present M.Sc. thesis is the developpement of an efficient and fast methodology toward the production of highly substituted allenes using enantioenriched cyclopropanes derivatives. The development of new synthetic methodologies in the production of these enantioenriched cyclopropan-1,1-diesters will be presented. First, the various methodologies for the preparation of activated cyclopropanes will be discussed along with their uses in the synthesis of more complex molecules. Then, the precedents in the field of asymmetric allenes synthesis will be introduced. The developpement of a viable method for the synthesis of cyclopropane-1,1-diesters using iodonium ylides will be presented. Finally, the accessibility of different highly substituted allenes by the used of cuprates will be detailed. In a second part, we will elaborate on the accessibility of the enantioenriched cyclopropane-1,1-diesters derivatives. These compounds are interesting, because they are used as starting materials in the previous methodology of allenes synthesis. This methodology has to be usable in large scale and at small cost. The last two chapters of this thesis will present the alternatives strategies for the preparation of these activated cyclopropanes by either kinetic resolution or the asymmetric hydrogenation of cyclopropenes.
Części książek na temat "Cuprate addition"
Grenier, J. C., F. Arrouy, J. P. Locquet, C. Monroux, M. Pouchard, A. Villesuzanne i A. Wattiaux. "The Role of The Additional Oxygen Atoms on the Superconducting Properties of La2CuO4-Related Compounds". W Phase Separation in Cuprate Superconductors, 236–56. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78805-5_18.
Pełny tekst źródłaZimmer, R. "Cuprate Addition and Silylation of Alkyl Propynoates". W Three Carbon-Heteroatom Bonds: Ketenes and Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00053.
Pełny tekst źródłaTaber, Douglass. "The Kobayashi Synthesis of (-)-Norzoanthamine". W Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0105.
Pełny tekst źródłaTaber, Douglass. "C-O Ring Containing Natural Products: Paeonilactone B (Taylor), Deoxymonate B (de la Pradilla), Sanguiin H-5 (Spring), Solandelactone A (White), Spirastrellolide A (Paterson)". W Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0050.
Pełny tekst źródłaKresin, Vladimir Z., Sergei G. Ovchinnikov i Stuart A. Wolf. "Experimental Methods". W Superconducting State, 201–27. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780198845331.003.0004.
Pełny tekst źródłaTaber, Douglass F. "Metal-Mediated Carbocyclic Construction: The Whitby Synthesis of (+)-Mucosin". W Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0075.
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