Relevant bibliographies by topics / Addition de Michael diastéréosélective

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  2. Dissertations / Theses
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Academic literature on the topic 'Addition de Michael diastéréosélective'

Author: Grafiati
Published: 4 June 2021
Last updated: 3 February 2022

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Journal articles on the topic "Addition de Michael diastéréosélective"

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Pourcelot, G., J. Aubouet, A. Caspar, and P. Cresson. "Addition diastéréosélective d'organo-cuprates à des imides chirales insaturées." Journal of Organometallic Chemistry 328, no. 3 (July 1987): C43—C45. http://dx.doi.org/10.1016/0022-328x(87)80264-4.

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Pourcelot, G., O. Melnyk, Y. Besace, E. Stephan, and P. Cresson. "Addition diastéréosélective d'allyl cuprates à des imides chirales insaturées." Journal of Organometallic Chemistry 388, no. 1-2 (May 1990): c5—c8. http://dx.doi.org/10.1016/0022-328x(90)85369-a.

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Thanupran, Chatchai, Chachanat Thebtaranonth, and Yodhathai Thebtaranonth. "Stereospecific triple Michael addition." Tetrahedron Letters 27, no. 20 (1986): 2295–98. http://dx.doi.org/10.1016/s0040-4039(00)84512-8.

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Liao, Xi-Bin, Ji-Ye Han, and Ying Li. "Michael addition of artemisitene." Tetrahedron Letters 42, no. 15 (April 2001): 2843–45. http://dx.doi.org/10.1016/s0040-4039(01)00310-0.

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Reuter, Carin, and Fritz Vögtle. "Rotaxanes via Michael Addition†." Organic Letters 2, no. 5 (March 2000): 593–95. http://dx.doi.org/10.1021/ol990350u.

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Feil, Sylvia. "Wundverschluss durch Michael-Addition?" Chemie in unserer Zeit 39, no. 4 (August 2005): 233. http://dx.doi.org/10.1002/ciuz.200590050.

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Thirumalaikumar, Muniappan. "Enantioselective Michael Addition Reactions." Organic Preparations and Procedures International 43, no. 1 (February 10, 2011): 67–129. http://dx.doi.org/10.1080/00304948.2011.547102.

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Jha, S. C., and N. N. Joshi. "Catalytic, enatioselective Michael addition reactions." Arkivoc 2002, no. 7 (September 20, 2002): 167–96. http://dx.doi.org/10.3998/ark.5550190.0003.718.

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Trumbo, David L. "Michael addition polymers from bisacetoacetates." Polymer Bulletin 26, no. 5 (September 1991): 481–85. http://dx.doi.org/10.1007/bf01032670.

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Chen, Bi-Shuang, Verena Resch, Linda G. Otten, and Ulf Hanefeld. "Enantioselective Michael Addition of Water." Chemistry - A European Journal 21, no. 7 (December 21, 2014): 3020–30. http://dx.doi.org/10.1002/chem.201405579.

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Dissertations / Theses on the topic "Addition de Michael diastéréosélective"

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Gendron, Thibault. "Synthesis and evaluation of the antiparasitic activity of diarylideneacetones and their related thiopyranone and S-oxide prodrugs." Thesis, Strasbourg, 2012. http://www.theses.fr/2012STRAF064/document.

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La trypanosomiase humaine africaine, la maladie de Chagas et les leishmanioses sont des maladies parasitaires qui représentent un problème majeur de santé publique dans de nombreux pays et notamment ceux en voie de développement. Afin de trouver de nouveaux candidat-médicaments contre ces parasites, deux séries chimiques ont été étudiées : les diarylidèneacétones et les 2,6-diaryl-4H-tetrahydrothiopyranones.Précédemment initiée au laboratoire, l'étude approfondie de la série diarylidèneacétone a nécessité la mise au point et l'optimisation de protocoles. Une nouvelle méthodologie de synthèse des (hétéro)diarylidèneacétones dissymétriques par palladocatalyse a ainsi été développée en collaboration avec le Pr. T. J. Müller (Université de Düsseldorf). En dépit d'excellentes activités antiparasitaires, la plupart des diarylidèneacétones synthétisées se sont révélées trop toxiques sur les cellules humaines.Les 2,6-diaryl-4H-tétrahydrothiopyranones et leurs S-oxydes ont été conçues pour résoudre ce problème de toxicité. Agissant comme prodrogues, ces molécules sont susceptibles de régénérer les diarylidèneacétones parentes par β-élimination du groupement soufré intracyclique. Peu décrite dans la littérature, la synthèse diastéréosélective de ces structures a été intégralement mise au point et généralisée à de nombreuses substitutions. Les résultats obtenus prouvent que la toxicité des produits a été grandement diminuée tout en maintenant une activité antiparasitaire importante, ce qui valide l'approche de la stratégie prodrogue
Human African trypanosomiasis, Chagas disease and leishmaniasis are parasitic diseases that significantly affect the populations and thus the economy of many developing countries. With the aim of developing new therapeutic agents to cure these diseases, we focused our research on two series: the diarylideneacetone and the 2,6-diaryl-4H-tetrahydrothiopyranone series.To complete and expend preliminary results that had been previously obtained in our laboratory, a generalization and an optimization of the protocols was intended. Thus, a novel Palladium-catalyzed synthesis of (hetero)dissymmetric diarylideneacetones was developed and optimized in collaboration with Prof. T. J. Müller (University of Düsseldorf). In spite of excellent antiparasitic activities, most of the diarylideneacetones were toxic toward human cells.2,6-Diaryl 4H-tetrahydrothiopyranones and their related S-oxides were designed to cope with major toxicity issues. Acting as prodrugs, these molecules are prone to undergo β-elimination of the sulfurated intracyclic group, regenerating the parent diarylideneacetone. The diastereoselective synthesis of this scaffold is not extensively described in the literature. Consequently, novel diastereoselective methodologies have been developed and generalized to a wide panel of substitution patterns. Results of the biological assays demonstrated that sulfide and S-oxide prodrugs displayed a lowered toxicity while the potency was maintained, thus confirming the validity of the prodrug strategy
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Toueg, Julie. "Vers la synthèse du tricylce ABC de l'acide hexacyclinique." Phd thesis, Ecole Polytechnique X, 2007. http://pastel.archives-ouvertes.fr/pastel-00003153.

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Au cours de ces travaux de thèse, nous avons exploré diverses voies de synthèse du tricycle ABC de l'acide hexacyclinique, une molécule isolée en 2000 d'une souche de Streptomyces et possédant une activité cytotoxique modérée. Dans un premier temps nous avons mis au point une synthèse rapide et efficace de 2 précurseurs du cycle A, dont l'étape clé est une nouvelle réaction de métathèse cyclisante. Puis nous avons poursuivi notre synthèse selon un premier chemin synthétique dont les étapes clés sont une addition de Michael hautement diastéréosélective avec un énolate tricyclique ponté, et une cyclisation radicalaire initiée par l'acétate de manganèse (III). Après une optimisation préalable de l'addition de Michael sur un modèle racémique, cette voie nous a permis de synthétiser un précurseur avancé du tricycle ABC. Nous avons également testé l'emploi d'un énolate moins encombré pour l'étape clé d'addition de Michael, dont les rendements obtenus précédemment s'avéraient insuffisants dans le cadre d'une synthèse totale. Cette nouvelle voie nous a permis d'obtenir avec de meilleurs résultats un deuxième précurseur avancé du tricycle ABC, possédant tous les centres stéréogènes requis. Enfin, nous avons développé une nouvelle méthodologie permettant d'accéder au motif α-carbalcoxyénone cyclique. Elle permet de former de manière efficace des cycloalcénones à 5 ou 6 chaînons à l'aide d'une réaction de métathèse cyclisante impliquant une oléfine doublement désactivée par un groupement carbonylé. L'utilité de cette méthodologie a été démontrée par plusieurs applications synthétiques.
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Castelot-Deliencourt, Géraldine. "Synthèse diastéréosélective de composés amidophosphorés : accès à des molécules biologiquement actives et à des ligands pour la catalyse asymétrique." Rouen, 2000. http://www.theses.fr/2000ROUES067.

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L'objectif de ce travail était de développer une nouvelle méthodologie de création de centre asymétrique en de l'atome de phosphore sur des composés amidophosphorés. Dans la première partie, nous nous sommes intéressés a des α-amidophosphonates. L'introduction du centre asymétrique a été envisagée par des réactions d'alkylation diastéréosélective en utilisant un aminoalcool comme copule chiral. Dans une seconde partie, notre étude s'est orientée sur des β-amidophosphonates et phosphines afin de développer une voie d'accès respectivement à des composés biologiquement actifs et à des ligands utilisables en catalyse asymétrique. La création du centre asymétrique sur ces composés a été envisagée soit par des réactions de métallation alkylation ou par des réactions d'addition 1,4- diastéréosélective en utilisant des aminoalcools ou des dérivés comme inducteur de la chiralité. Les premiers essais d'élimination des différentes copules chirales ont été aussi réalisés.
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Santoro, Francesco. "Ruthenium/PNNP-catalyzed asymmetric Michael addition /." Zürich : ETH, 2007. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=17024.

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Poderi, Cecilia. "Synergistic catalysis: Michael addition of acyl-pyridines." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2017. http://amslaurea.unibo.it/14409/.

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A new diastereo- and enantioselective strategy for the functionalization of 2-acetyl-pyridine with α,β-unsaturated aldehydes has been investigated through synergistic catalysis. In particular, the aim of the work was to use cinnamaldehydes bearing different substituents on the phenyl group and to study its effect on the yield, conversion and stereoselectivity of the reaction. The reaction mechanism involves combined iminium ion and transition metal catalysis in a synergistic fashion and proceeds with two consecutives Michael additions, followed by final intramolecular aldol condensation to yield the formation of three new stereogenic carbons, with high to excellent stereoselectivities. The structures of the molecules obtained were fully characterized by NMR spectroscopy. After having assigned the relative configuration by NOE-NMR and 2D-COSY experiments, conformational analysis was performed by DFT calculations to find the most stable molecular conformations. The absolute configuration of each diastereoisomer was then eventually assigned by quantum mechanical simulations of the Electronic and Vibrational Circular Dichroism spectra.
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Rotulo-Sims, Delphine. "Synthèse diastéréosélective de diols-1,3 et de triols-1,3,5 à partir de vinyl sulfones." Palaiseau, Ecole polytechnique, 2005. http://www.theses.fr/2005EPXX0008.

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Chaumette, Jean-Louis. "Synthèse asymétrique d'acides α-halogénés par halogénation diastéréosélective d'acétals de cétènes silylés ; addition asymétrique d'alcools sur des cétènes α-halogénés." Rouen, 1996. http://www.theses.fr/1996ROUES052.

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Le potentiel des hydrates de carbones et plus particulièrement des acétals du glucose lorsqu'ils sont utilisés en tant qu'auxiliaires chiraux dans une réaction de synthèse asymétrique a été montré au cours de ce travail : il a été utilisé comme inducteur de chiralité pour la synthèse d'acides α-halogénés. Ainsi l'halogénation diastéréoselective d'acétals de cétènes trialkyl silylés dérivés du glucose permet d'accéder aux (S)-2-chloro-acides avec des excès énantiomèriques allant jusqu'à 95% et aux (S)-2-bromoacides avec une pureté énantiomèrique allant jusqu'à 85%. D'autre part, l'addition asymétrique de dérivés du glucose sur des cétènes α-halogénées permet d'accéder aux acides α-halogénés avec des excès énantiomèriques allant jusqu'à 78%. L'étude structure-stéréosélectivité que nous avons menée sur ces deux réactions a permis de mettre en évidence l'origine des hautes stéréosélectivités observées. Une région d'interaction favorable dans l'auxiliaire chiral a été mise en évidence ce qui a permis de réaliser la synthèse de structures simplifiées du L-glucose. L'halogénation des acétals de cétènes correspondant permet d'accéder aux (R) α-halogénoacides avec des excès énantiomèriques allant jusqu'a 90%, et l'addition des équivalentes du L-glucose sur des cétènes α-halogénés permet d'accéder aux (R)- α halogénoacides avec une pureté énantiomèrique allant jusqu'à 72%.
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Pelzer, Silke. "Wie es geht eine quantenchemische Untersuchung der eisenkatalysierten Michael-Reaktion /." [S.l.] : [s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=971232482.

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Saraiva, rosa Nathalie. "Synthèse diastéréosélective de molécules azotées α-trifluorométhylées - Élaboration et études conformationnelles de petits peptides incorporant des acides β-aminés trifluorométhylés." Thesis, Reims, 2017. http://www.theses.fr/2017REIMS013.

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Les N-tert-butanesulfinamides, des auxiliaires chiraux développés par Ellman il y a une vingtaine d’années, sont à l’heure actuelle de plus en plus sollicités pour la préparation d’amines chirales fonctionnalisées, et ce, du fait de la disponibilité des deux énantiomères à faible coût et de leurs conditions de déprotection faciles à mettre en œuvre. Cependant, leur utilisation dans le cadre de la synthèse de dérivés trifluorométhylés quaternaires à partir des N-tert-butanesulfinylalkyl- ou arylcétimines correspondantes, connues pour leur faible hydrostabilité, reste à ce jour très limitée. Les éthers d’hémiaminals trifluorométhylés dérivés de l’auxiliaire d’Ellman constituent des analogues stables de ces cétimines. Ils permettent de générer in situ la cétimine correspondante, qui peut subir l’addition de l’espèce nucléophile présente. Ce manuscrit relate les différentes réactions étudiées sur ces éthers d’hémiaminals, donnant ainsi accès à des synthons azotés α-trifluorométhylés quaternaires de façon énantiopure : d’une part, les amines homoallyliques obtenues par l’addition d’allylalanes, qui, après quelques étapes, permettent de fournir les azétidines trifluorométhylées correspondantes, et d’autre part, les β3,3-aminoacides trifluorométhylés, préparés via une réaction de Reformatsky hautement diastéréosélective. Les acides β-aminés ainsi préparés ont été réinvestis dans des couplages peptidiques en solution pour la préparation d’une gamme d’α/β- et de β-di- et tripeptides, sur lesquels des études conformationnelles préliminaires ont été menées à l’état solide et/ou en solution.Mots-clés : Auxiliaire d’Ellman, Addition nucléophile, Couplage peptidique en solution, Dérivé azoté α-trifluorométhylé, Éther d’hémiaminal, Synthèse asymétrique
Chiral N-tert-butansulfinamides, developped by Ellman 20 years ago, have been increasingly applied for the preparation of chiral functionnalized amines, because of the affordability of both enantiomers and of their mild conditions of cleavage. However, the use of theses auxiliaries for the synthesis of quaternary trifluoromethyl derivatives remains quite limited, the corresponding trifluoromethyl ketoimines being highly unstable.Chiral N-tert-butanesulfinyl alkyl(aryl) trifluoromethyl hemiaminal ethers have been developped to be used as bench-stable surrogates of these ketoimines : once under reaction conditions, they afford the corresponding ketoimine in situ, which can be subject to a nucleophilic addition.In this manuscript, different reactions led on these hemiaminal ethers are described, affording valuable and optically pure trifluoromethylated quaternary building-blocks : on the one hand, homoallylic amines, obtained by the addition of allylalane species, and which can afford, after a few steps, teh corresponding trifluoromethyl azetidines, and on the other hand, chiral trifluoromethyl β3,3-amino acids, afforded by a highly diastereoselective Reformatsky reaction.These β 3,3-amino acids have been then involved in solution-phase peptide couplings in order to synthetise a wide range of α/β- and β-di- and tripeptides, whose conformation have been the object of preliminary studies in the solid state and/or in solution.Key-words : Ellman auxiliary, Nucleophilic addition, Solution-phase peptide coupling, α-trifluoromethylated nitrogen derivative, Hemiaminal ether, asymmetric synthesis
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Schmidt, Christian. "Darstellung konformativ eingeschränkter Glutaminsäurederivate durch Michael-Addition von chelatisierten Glycinesterenolaten." [S.l.] : [s.n.], 2007. http://deposit.ddb.de/cgi-bin/dokserv?idn=984726101.

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Books on the topic "Addition de Michael diastéréosélective"

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Heo, Christina K. M. Quantitative studies on the addition of pyridines to Michael acceptors. Ottawa: National Library of Canada, 1990.

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Heo, Christina K. M. Quantitative studies on the addition of amine nucleophiles to Michael acceptors. 1993.

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Borelli, Melissa Blanco. Introduction. Edited by Melissa Blanco Borelli. Oxford University Press, 2014. http://dx.doi.org/10.1093/oxfordhb/9780199897827.013.004.

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In addition to providing an overview of the chapters that comprise the volume, this chapter uses a music video by George Michael as an example of how to engage students in dance studies analysis of bodies on the popular screen. It also provides an overview to students on how they might engage with the bodies and the choreographies they see on the screen.
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Kymlicka, Will. Contemporary Political Philosophy. Oxford University Press, 2017. http://dx.doi.org/10.1093/hepl/9780198782742.001.0001.

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Contemporary Political Philosophy has been revised to include many of the most significant developments in Anglo-American political philosophy in the last eleven years, particularly the new debates on political liberalism, deliberative democracy, civic republicanism, nationalism, and cultural pluralism. The text now includes two new chapters on citizenship theory and multiculturalism, in addition to updated chapters on utilitarianism, liberal egalitarianism, libertarianism, socialism, communitarianism, and feminism. The many thinkers discussed include G. A. Cohen, Ronald Dworkin, William Galston, Carol Gilligan, R. M. Hare, Catherine Mackinnon, David Miller, Philippe Van Parijs, Susan Okin, Robert Nozick, John Rawls, John Roemer, Michael Sandel, Charles Taylor, Michael Walzer, and Iris Young.
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Trültzsch-Wijnen, Christine, and Gerhard Brandhofer, eds. Bildung und Digitalisierung. Nomos Verlagsgesellschaft mbH & Co. KG, 2020. http://dx.doi.org/10.5771/9783748906247.

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This volume discusses the challenges posed by digitalisation in the field of education from different professional perspectives. Authors from various disciplines analyse general theoretical questions, present current empirical findings, discuss didactic models and projects, and consider the use of digital media in tertiary education. In addition, they present specific projects from educational practice. With contributions by Alessandro Barberi, Gerhard Brandhofer, Josef Buchner, Markus Ebner, Martin Ebner, Nicole Duller, Walter Fikisz, Sonja Gabriel, Barbara Getto, Nina Grünberger, Elke Höfler, Fares Kayali, Michael Kerres, Philipp Leitner, Peter Micheuz, Marlene Miglbauer, Thomas Nárosy, Daniel Otto, Alexander Pfeiffer, Claudia Schreiner, Carmen Sippl, Elke Szalai, Caroline Roth-Ebner, Karin Tengler, Manfred Tetz, Christine W. Trültzsch-Wijnen, Thomas Wernbacher, Christian Wiesner
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Schaupp, Walter, and Johann Platzer, eds. Der verbesserte Mensch. Nomos Verlagsgesellschaft mbH & Co. KG, 2020. http://dx.doi.org/10.5771/9783748910565.

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The phenomenon of increasing optimisation and transformation of the human body using modern biotechnologies is encountered in various fields. In addition to interference with the human genome, attempts to merge man and machine are becoming increasingly important. Since the idea of an inviolable form of human ‘nature’ has been lost, new philosophical and ethical efforts are required in order to meet the challenges associated with it. In this book, the topics of transhumanism, humans and machines, genome editing, sex reassignment and the issue of enhancing happiness through biotechnological means are discussed and reflected on ethically. With contributions by Alois Birklbauer, Christian Egarter, Reinhold Esterbauer, Johann Platzer, Andreas Reinisch, Michael Rosenberger, Walter Schaupp, Peter Strasser, Gunda Werner.
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Schultz, Jaime. Epilogue. University of Illinois Press, 2017. http://dx.doi.org/10.5406/illinois/9780252038167.003.0009.

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This concluding chapter considers the status of women's sports in 2012, the various points of change that brought them there, and reasserts the need to cheer with reserve. Even as the number of women athletes seems to rise, their representation in administrative ranks has dwindled from the pre-Title IX era. In addition, sports sociologists Michael Messner and Cheryl Cooky found that there has been a “precipitous decline” in the amount of television coverage devoted to women's sports over the past several years. In 2009 women's sports garnered just 1.6 percent of network sports news and 1.4 percent of ESPN's SportsCenter. For a brief window in July 2012, however, those numbers temporarily increased as the world tuned in to the Women's Games.
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Löwe, Matthias, and Gideon Stiening, eds. Ästhetische Staaten. Nomos Verlagsgesellschaft mbH & Co. KG, 2021. http://dx.doi.org/10.5771/9783845277813.

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Friedrich Schiller, the grand master of the classical aesthetic of autonomy, was also a political thinker. In the 1790s, reading Immanuel Kant upset him, as did the French Revolution: abuse of power, political resistance, conspiracy and tyrannicide are just a few of the genuinely political themes that he repeatedly varies in literary terms. The articles in this volume consider the connection between the political, legal and ethical dimensions of Schiller's work. In addition to his 'big' dramas as well as his philosophical and historical writings, they examine the nexus of ethics, law and politics at the 'margins' of his work, in both his short works and his literary fragments. With contributions by Oliver Bach, Antonino Falduto, Maria Carolina Foi, Markus Hien, Matthias Löwe, Vincenz Pieper, Jens Ole Schneider, Michael Schwingenschlögl, Sebastian Speth, Gideon Stiening and Ludwig Stockinger.
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Gereboff, Joel. Judaism. Edited by John Corrigan. Oxford University Press, 2009. http://dx.doi.org/10.1093/oxfordhb/9780195170214.003.0006.

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The emotions are an important feature of Jewish life and thought throughout the ages. From biblical descriptions of a God of pathos to early rabbinic and medieval works detailing the virtues, to mystical tracts focused on the inner life, and occasionally portraying emotion filled religious experiences of the adept, there have always been Jewish representations of the affective dimensions of life. In addition, the many ways Jews have actually participated in prayer and in the celebration of holidays, and in the construction of material objects and spaces in which such activities took place, also give evidence of emotional texture of the lives of Jews. John Corrigan's concluding observations in his introduction to Religion and Emotion: Approaches and Interpretations, in which he sets forth a model for future scholarship in this field, provide a standard against which to assess present investigations into Judaism and the emotions. Others who have produced methodologically astute scholarship adding significantly to the understanding of aspects of Jewish thought on the emotions are Michael Fishbane, Daniel Boyarin, and Hava Tirosh-Samuelson.
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Ahmed, Mohamed. Arabic in Modern Hebrew Texts. Edinburgh University Press, 2019. http://dx.doi.org/10.3366/edinburgh/9781474444439.001.0001.

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In the late 1950s, Iraqi Jews were either forced or chose to leave Iraq for Israel. Finding it impossible to continue writing in Arabic in Israel, many Iraqi Jewish novelists faced the literary challenge of switching to Hebrew. Focusing on the literary works of the writers Shimon Ballas, Sami Michael and Eli Amir, this book examines their use of their native Iraqi Arabic in their Hebrew works. It examines the influence of Arabic language and culture and explores questions of language, place and belonging from the perspective of sociolinguistics and multilingualism. In addition, the book applies stylistics as a framework to investigate the range of linguistic phenomena that can be found in these exophonic texts, such as code-switching, borrowing, language and translation strategies. This new stylistic framework for analysing exophonic texts offers a future model for the study of other languages. The social and political implications of this dilemma, as it finds expression in creative writing, are also manifold. In an age of mass migration and population displacement, the conflicted loyalties explored in this book through the prism of Arabic and Hebrew are relevant in a range of linguistic contexts.
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Book chapters on the topic "Addition de Michael diastéréosélective"

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Li, Jie Jack. "Michael addition." In Name Reactions, 232. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_182.

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Li, Jie Jack. "Michael addition." In Name Reactions, 355–56. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_160.

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Li, Jie Jack. "Michael addition." In Name Reactions, 397–98. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_173.

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Li, Jie Jack. "Michael addition." In Name Reactions, 260. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_193.

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Li, Jie Jack. "Michael Addition." In Name Reactions, 348–51. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_93.

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Li, Jie Jack. "Mukaiyama Michael addition." In Name Reactions, 377–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_171.

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Li, Jie Jack. "Mukaiyama Michael addition." In Name Reactions, 419–20. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_184.

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Li, Jie Jack. "Mukaiyama Michael Addition." In Name Reactions, 373–75. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_100.

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Spitzner, D., and P. Wagner. "Lewis Acid Catalized Double Michael Addition." In Selectivities in Lewis Acid Promoted Reactions, 323. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2464-2_30.

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Oare, David A., and Clayton H. Heathcock. "Stereochemistry of the Base-Promoted Michael Addition Reaction." In Topics in Stereochemistry, 227–407. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470147283.ch5.

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Conference papers on the topic "Addition de Michael diastéréosélective"

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Carvalho, Pedro H. P. R., Alexandre F. Gomes, Luciana M. Ramos, Fábio C. Gozzo, Eufrânio N. da Silva Júnior, and Brenno A. D. Neto. "ESI-IMS-QTOF: a regioselective Michael addition study." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0224-2.

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Feu, Karla S., Sandrina I. R. M. Silva, Marco A. F. M. Junior, Alexander F. de la Torre, Arlene G. Corrêa, and Márcio W. Paixão. "PEG: An Efficient Green Solvent for Organocatalytic Asymmetric Michael Addition." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013820194343.

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Chigorina, Elena, and Victor Dotsenko. "The Michael-type Addition of 1-Cyanoacetyl-3,5-dimethylpyrazole to Arylmethylenecyanoacetamides." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a045.

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Iida, Hirokazu, and Kie Takahashi. "Michael addition of anilines or phenols without solvent under microwave irradiation." In 2016 Progress in Electromagnetic Research Symposium (PIERS). IEEE, 2016. http://dx.doi.org/10.1109/piers.2016.7735579.

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Ferreira*, Misael, and Marcus Mandolesi Sá. "Intramolecular Aza-Anti-Michael Addition for the Synthesis of 2-Iminothiazolidines." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013819173959.

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Chu, Xi, John J.La Scala, and Giuseppe Palmese. "Bio-Based Thermosets Prepared Using Michael Addition of Furan and Isosorbide Building Blocks." In SAMPE 2019 - Charlotte, NC. SAMPE, 2019. http://dx.doi.org/10.33599/nasampe/s.19.1515.

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Daďová, Jitka, Petr Orság, Radek Pohl, Marie Brázdová, Miroslav Fojta, and Michal Hocek. "Study of DNA-protein interactions by cross-link formation using aqueous Michael addition." In XVIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414240.

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Scatena, Gabriel dos S., Alexander F. De la Torre, Quezia B. Cass, and Márcio W. Paixão. "Silica-Supported Prolyl Pseudo-Peptide Organocatalysts: Application in the Direct Asymmetric Michael Addition." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013915204013.

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Zhao, Dishun, and Xiaolei Bao. "Synthesis of Eco-Friendly Ionic Liquids by Microwave Irradiation and Their Applications in Michael Addition." In 2009 3rd International Conference on Bioinformatics and Biomedical Engineering (iCBBE 2009). IEEE, 2009. http://dx.doi.org/10.1109/icbbe.2009.5163555.

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Torre, Alexander F. de la, Daniel G. Rivera, Marco A. B. Ferreira, Arlene G. Corrêa, and Márcio W. Paixão. "Multicomponent Combinatorial Development of Prolyl Pseudo- Peptide Catalysts: Application in the Direct Asymmetric Michael Addition." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201383174130.

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You might also be interested in the extended bibliographies on the topic 'Addition de Michael diastéréosélective' for particular source types:
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