Готові списки джерел за темами / Michael's Addition

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  1. Статті в журналах
  2. Дисертації
  3. Книги
  4. Частини книг
  5. Тези доповідей конференцій

Добірка наукової літератури з теми "Michael's Addition"

Автор: Grafiati
Опубліковано: 23 вересня 2022
Оновлено: 28 січня 2023

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Статті в журналах з теми "Michael's Addition"

1

Urosevic, Jovica, Sasa Drmanic, Jasmina Nikolic, Ivan Juranic, and Bratislav Jovanovic. "Structure-reactivity correlation for the kinetics of the reaction of substituted 4-phenyl-1,4-dihydropyridines formation." Journal of the Serbian Chemical Society 78, no. 12 (2013): 1963–73. http://dx.doi.org/10.2298/jsc131120139u.

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Quantitative structure-reactivity correlations for the kinetics of the Hantzsch's synthesis of substituted 4-phenyl-1,4-dihydropyridines in the reaction between ethyl m- and p-substituted benzylidene acetoacetate and enamine has been studied. The reaction kinetics was followed using spectrophotometric measurements. It was found that the reaction correspond to the second-order kinetics. Quantitative structure-reactivity correlations of log k with the corresponding substituent constants (s,s+,sI and sR+) using Hammett and extended Hammett equation (DSP equation). They show linear relationship with positive values of reaction constants (r). The obtained data were processed by the linear regression analysis. It is confirmed that Michael's addition of enamine to benzylidene represents the slow step of the reaction with high positive charge at the benzylidene molecule. MO calculations were performed and they were also in agreement with the conclusions derived from structure-reactivity correlations.
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2

BOZKURT, Selahattin. "Asimetrik Michael Katılma Tepkimesi için Prolin bazlı β-Hidroksiamit Organokatalizörü". Afyon Kocatepe Üniversitesi Uluslararası Mühendislik Teknolojileri ve Uygulamalı Bilimler Dergisi 5, № 1 (15 червня 2022): 13–17. http://dx.doi.org/10.53448/akuumubd.1111800.

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Applications of chiral organocatalysts in reaction types capable of forming C-C bonds, such as Michael addition, are one of the important research areas of recent years. One of the best examples of Michael addition, one of the important works of organic reaction types, is the reaction of nitroolefins with ketones in the presence of organocatalysts. In this study, L-proline-based amide derivative was synthesized with moderate yield and its structure was elucidated by various techniques. As an organocatalyst, its effect on enantiomeric excess (e.e.) was investigated in Michael addition studies and the best enantiomeric excess value was found to be 65% in carbontetra chloride (CCl4).
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3

Naghiyev, F. N. "THE INVESTIGATION OF MICHAEL ADDITION OF ACETOACETANILIDE AND METHYL ACETOPYRUVATE TO SOME YLIDENECYANOACETAMIDES." Azerbaijan Chemical Journal, no. 2 (June 20, 2019): 35–39. http://dx.doi.org/10.32737/0005-2531-2019-2-35-39.

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4

Bansal, Shobha, and Prabal Pratap Singh. "An Efficient Solvent Free Microwave Assisted MgFe2O4 Magnetic Nanoparticles Catalyzed Green Protocol Towards Michael Addition." Chemistry & Chemical Technology 13, no. 1 (March 5, 2019): 18–22. http://dx.doi.org/10.23939/chcht13.01.018.

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5

Emori, Eita, Takayoshi Arai, Hiroaki Sasai та Masakatsu Shibasaki. "A Catalytic Michael Addition of Thiols to α,β-Unsaturated Carbonyl Compounds: Asymmetric Michael Additions and Asymmetric Protonations". Journal of the American Chemical Society 120, № 16 (квітень 1998): 4043–44. http://dx.doi.org/10.1021/ja980397v.

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6

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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7

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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8

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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9

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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10

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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Дисертації з теми "Michael's Addition"

1

Clement, Baptiste. "Nouvelles résines sans isocyanates réactives à basses températures pour revêtements elastomères durables." Thesis, Mulhouse, 2020. http://www.theses.fr/2020MULH4567.

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L’objectif de la thèse est d’explorer de nouveaux systèmes chimiques à réactivité élevée à température ambiante et les soumettre à un cahier des charges de polymères thermodurcissables. Ce projet a été construit autour de deux chimies capables de s’effectuer dans des conditions douces : l’addition d’aza-Michael et la cycloaddition de Diels-Alder. L’addition d’aza-Michael est une réaction spontanée à température ambiante, s’effectuant entre une fonction amine et un composé  insaturé comme les acrylates. Cette réaction peut être réalisée sans solvants ni catalyseurs. Elle est donc couramment utilisée depuis de nombreuses années dans le domaine des polymères. Une autre voie faisant également l’objet de nombreuses études dans les thermodurcissables est la réaction de cycloaddition de Diels-Alder, s’effectuant entre un diène et un diénophile. L’avantage de cette réaction est son caractère potentiellement réversible, effectif à partir de températures supérieures à 100°C. Les travaux de la thèse ont été divisés en deux chapitres importants dans lesquels l’addition d’aza-Michael a été principalement utilisée. Un premier chapitre a été consacré au développement de nouveaux systèmes mono-composants, et l’autre à l’obtention de systèmes bi-composants. Pour la première partie, différents systèmes mono-composants ont été préparés par addition de Michael. Concernant le deuxième chapitre, une partie a été dédiée à l’utilisation de la cycloaddition de Diels-Alder pour l’obtention de matériaux réticulés. L’autre partie s’est consacrée à l’emploi de l’addition aza-Michael via plusieurs systèmes de réticulation
The aim of the thesis is to explore new chemical systems with high reactivity at room temperature and to submit them to coatings specifications. Two chemicals reactions performing under mild conditions was used : the aza michael additionn and the Diels-Alder cycloaddition. The aza-Michael addition is a spontaneous reaction at room temperature between an amine function and an  unsaturated compound such as acrylates. This reaction can be carried out without solvents or catalysts. The other one that has also been the subject of numerous studies in thermosets field is the Diels-Alder cycloaddition reaction, carried out between a diene and a dienophile. The advantage of this reaction is its potentially thermo-reversible nature.The work of the thesis was divided into two important parts in which the aza-Michael addition was mainly used. The first chapter was devoted to the development of one-component systems, and the other one to the production of two-component systems. For the first chapter, several one-component systems have been prepared by Michael addition. Concerning the second chapter, a part was dedicated to the use of the Diels-Alder cycloaddition for obtaining thermosets. The other part is devoted to the use of aza-Michael addition via several crosslinking systems
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2

Schultz, Alison. "From Block Copolymers to Crosslinked Networks: Anionic Polymerization Affords Functional Macromolecules for Advanced Technologies." Diss., Virginia Tech, 2016. http://hdl.handle.net/10919/81835.

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Ion-containing macromolecules continue to stimulate new opportunities for emerging electro-active applications ranging from high performance energy devices to water purification membranes. Progress in polymer synthesis and engineering now permit well-defined, ion-containing macromolecules with tunable morphologies, mechanical performance, ion conductivity, and 3D structure in order to address these globally challenged technologies. Achieving tailored chemical compositions with high degrees of phase separation for optimizing conductivity and water adsorption remains a constant synthetic challenge and presents an exciting opportunity for engineering sophisticated macromolecular architectures. This dissertation will introduce unprecedented charged polymers using conventional free radical and anionic polymerization to incorporate ionic functionalities based on phosphonium cations. This new class of copolymers offers unique properties with ionic functionality for tailorable electro-active performance.
Ph. D.
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3

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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4

Young, Douglas M. "Explorations of Cascading Michael Additions." Thesis, University of Oregon, 2011. http://hdl.handle.net/1794/12069.

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xx, 214 p. : ill. (some col.)
Intramolecular cascading Michael additions have the ability to transform simple, symmetric substrates into densely functionalized compounds containing new ring structures and chiral centers. The Rauhut-Currier (RC) reaction, also known as the vinylogous Morita-Baylis-Hillman reaction, utilizes this type of reactivity by cyclizing tethered, activated alkenes using phosphine or thiolate catalysis. This dissertation describes the expansion of the scope of the RC reaction, the introduction and importance of co-catalysts to cascading Michael additions, the development of the first amine-catalyzed RC reaction, and the transformation of cyclization products into fused, polycyclic aromatic compounds. Chapter I reviews the development and applications of the Rauhut-Currier reaction. Chapter II describes the regioselective synthesis of di-substituted indenes and introduces phenol as a rate- and selectivity-enhancing co-catalyst. Although tertiary amine nucleophiles were found to be inferior to phosphines as cyclization catalysts, chapter III discusses the ability of unhindered primary and secondary amines to undergo a diastereoselective, cascading aza-Michael-Michael addition to yield a wide variety of amino-indanes in the presence of an acid catalyst. Recognizing the importance of protic environments and small nucleophiles, the development of the first amine-catalyzed intramolecular RC is introduced in chapter IV. Chapter V describes the conversion of methyl ketone-substituted indenes to fluorene derivatives via an intramolecular aldol reaction. Chapter VI describes the serendipitous discovery and synthesis of indenopyrylium salts. Chapter VII details the novel production of indenopyridines from di-substituted indenes. Lastly, chapter VIII provides a summary and suggests future directions for this research. This dissertation includes previously published and unpublished co-authored material.
Committee in charge: Shih-Yuan Liu, Chairperson; Kenneth Doxsee, Advisor; David Tyler, Member; Michael Haley, Member; A. Dana Johnston, Outside Member
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5

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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6

Chotsaeng, Nawasit. "Enantioselective rhodium-catalysed addition of allylboron reagents to cyclic imines and enantioselective nickel-catalysed Michael additions of 2-acetylazaarenes to nitroalkenes." Thesis, University of Edinburgh, 2016. http://hdl.handle.net/1842/16192.

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Rhodium-catalysed enantioselective allylation reaction of imines in the presence of chiral diene ligands has been investigated. Under the optimised conditions, cyclic imines provided homoallylic amines in high yield and excellent enantioselectivities. The reaction most likely proceeds via allylrhodium(I) intermediates, and represents the first rhodium-catalysed enantioselective nucleophilic allylation of π-electrophiles with allylboron compounds. Furthermore, the allylations display a strong preference for carbon–carbon bond formation at the more substituted terminus of the allyl fragment of the allyltrifluoroborate. To demonstrate the utility of the allylation products, representative manipulations were conducted. Enantioselective Nickel-Catalysed Michael Additions of 2-Acetylazaarenes to Nitroalkenes An enantioselective Michael addition of acylazaarenes with α-substituted β-nitroacrylates in the presence of a chiral Ni(II)–bis(oxazoline) complexes has been developed. A range of azaaryl nucleophiles were shown to react with a variety of nitroalkenes to construct highly functionalised Michael addition products which contain a stereogenic all-carbon quaternary stereocentre with moderate to high yields and enantioselectivities. A possible mechanism for this reaction has been proposed.
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7

Sawicki, Marcin. "Synthèse et criblage de ligands puissants de l'uranyle : application à la décorporation de l'uranium." Paris 11, 2005. http://www.theses.fr/2005PA112075.

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Ce travail de thèse, réalisé dans le cadre du programme " Toxicologie Nucléaire " du CEA, a été consacré à l'élaboration de ligands puissants de l'ion uranyle (UO22+) pour des applications de décorporation et à des fins analytiques. Suite à la mise au point d'une méthodologie de synthèse en mode parallèle, utilisant la réaction de Michael comme étape clé, une banque d'environ 200 molécules a été obtenue. Cette banque de ligands potentiels, ainsi que plus de 100 molécules obtenues par collaboration, ont été soumises à un test de criblage que nous avons également développé au laboratoire. Plus d'une vingtaine de ligands possédant des constantes de complexation pour l'ion uranyle supérieures à 10 puissance 17 ont ainsi été révélés à l'aide de ce criblage à haut débit. Toutes ces molécules se sont avérées être des structures possédant plusieurs motifs bis-phosphonates. Parmi elles, une seule présente des propriétés de décorporation in vivo. D'autre part, certains ligands bis-phosphoniques forment des complexes avec UO22+ ayant des propriétés de fluorescence remarquables et permettent d'améliorer les méthodes de détection de ce métal
This work was realised as a part of prorgamm "Nuclear Toxicologie" created by CEA and was dedicated to the synthesis of powerfull ligands of uranyl for the applications in decorporation and detection of uranyle. During this work about 200 new potentiales ligands of uranyle was synthesised in the parallele manner using as a key step of the synthesis peptide coupling as well as new parallel synthesis methodology based on the addition of Michael. This library of potencial uranyle ligands, enreached by 100 molecules obtained by collaboration, was submited to high throughput screening test for affinity against uranyle ion using colorimetric agent - sulfochlorophenole S as reference chelate. More then twenty ligands having conditional stability constant against uranyl at pH=7. 4 higher then 10 to 17 were found. All this molecules have methylene biphosphonate unite as chelating function. Beetwen them only one was foun to decorporate uranium in vivo. On the other hand some ligands methylene biphosphoniques were found to forme with uranyle ion the complexes posseding exceptional proprietes of fluorescence what may aloowed for their use for the detection of uranyle
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8

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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9

Howard-Jones, Andrew Glyn. "A synthetic approach to C←2 symmetric guanidine bases and the synthesis of model compounds of ptilomycalin A." Thesis, Bangor University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340956.

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10

Du, Haiying. "Michael addition-initiated organocatalytic enantioselective multicomponent reactions with 1,3-dicarbonyls." Thesis, Ecole centrale de Marseille, 2014. http://www.theses.fr/2014ECDM0002/document.

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Ce mémoire de thèse se concentre sur le développement de réactions multicomposants énantiosélectives de dérivés 1,3-Dicarbonylés en présence d'un organocatalyseur, en vue de préparer des motifs polyhétérocycliques fusionnés.Dans un premier temps, nous décrivons nos résultats initiaux sur une réaction multicomposants énantiosélective avec des énals et des amines primaires simples. Au vu des faibles énantiosélectivités obtenues, des amines fonctionnalisées ont ensuite été introduites dans ces réactions, permettant ainsi de synthétiser des pyrrolopiperazines et d'autres molécules hétérocycliques polyfonctionnalisées énantioenrichies, toutes obtenues avec des rendements intéressants et des énantiosélectivités élevées.Ayant utilisé avec succès des β-Cétoamides α-Méthyléniques dans ces réactions multicomposantes, nous avons réalisé par ailleurs que leur simple addition de Michael sur des oléfines pauvres en électrons n'avait jamais été décrite en version organocatalysée. Nous avons donc étudié leur réaction avec des nitrooléfines en présence d’organocatalyseurs chiraux, et les produits attendus ont alors été obtenus avec de bons rendements et d'excellentes diastéréo- et énantiosélectivités
This thesis focuses on the development of enantioselective multicomponent reactions with 1,3-Dicarbonyls in the presence of an organocatalyst, to synthesize fused polyheterocyclic motives.At first, we describe our initial results on an enantioselective multicomponent reaction with enals and simple primary amines. In view of the low enantioselectivities achieved, functionalized amines were then introduced in these reactions, thereby synthesizing enantioenriched pyrrolopiperazines and other polyfunctionalized heterocyclic molecules, all obtained with attractive yields and high enantioselectivities.Having successfully used methylene β-Ketoamides in these enantioselective MCRs, we realized also that their simple Michael addition to electron-Poor olefins had never been described in organocatalytic conditions. We therefore studied their reaction with nitroolefins in the presence of various chiral organocatalysts, and the expected products were pleasingly obtained with high yields, excellent diastereo- and enantioselectivities
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Книги з теми "Michael's Addition"

1

Frayn, Michael. The additional Michael Frayn. London: Methuen, 2000.

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2

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

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3

Day, Michael. Mont Orgueil Castle: Letter from Michael Day to Environment and Public Services with additional information, photographs and plans : re. Jersey Heritage Trust planning application. Jersey: Jersey Heritage Trust, 2003.

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4

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

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5

Wodhull, Michael. The Equality of Mankind: A Poem, by Michael Wodhull, Esq. Revised and Corrected, with Additions. Gale Ecco, Print Editions, 2018.

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6

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Oversight and Investigations., ed. Additional documents related to the subcommittee investigation of the activities of Michael K. Deaver and Associates. Washington: U.S. G.P.O., 1987.

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7

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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8

Kymlicka, Will. Contemporary Political Philosophy. Oxford University Press, 2017. http://dx.doi.org/10.1093/hepl/9780198782742.001.0001.

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Анотація:
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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9

K, Tweedie W. Calvin and Servetus : the Reformers Share in the Trial of Michael Servetus : Historically Ascertained from the French: With Notes and Additions. Independently Published, 2017.

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10

Marquardsen, Kai, ed. Armutsforschung. Nomos Verlagsgesellschaft mbH & Co. KG, 2022. http://dx.doi.org/10.5771/9783845299860.

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Анотація:
The perception of growing social insecurities and divisions, not least due to the Covid-19 pandemic, has brought questions of social inequality and poverty back into focus. The interdisciplinary handbook addresses these new and old challenges and at the same time critically classifies and interprets current developments and manifestations of poverty. In addition to the academic debate, the handbook shows perspectives for the socio-political treatment of poverty. It serves as a comprehensive and concise reference work for practitioners, students and academics at the interface of various social science sub-disciplines. With contributions by Jan Bertram, Peter Bescherer, Petra Böhnke, Jeanette Bohr, Rita Braches-Chyrek, Antonio Brettschneider, Karl August Chassé, Michael David, Sonja Fehr, Marion Fischer-Neumann, Yvonne Franke, Natalie Grimm, Viktoria Häußermann, Maren Hilke, Dennis Homann, Ernst-Ulrich Huster, Andrea Janßen, Nora Jehles, Petra Kaps, Michael Klassen, Tanja Kleibl, Bettina Kohlrausch, Daniel Kumitz, Lutz Leisering, Sigrid Leitner, Gaby Lenz, Stephan Lessenich, Ortrud Leßmann, Stephan Lorenz, Ronald Lutz, Kai Marquardsen, Michael May, Lars Meier, Maria Pernegger, Roswitha Pioch, Ayça Polat, Martin Schenk, Karin Scherschel, Daniela Schiek, Johannes Schütte, Frank Sowa, Anne Tittor, Athanasios Tsirikiotis, Carsten G. Ullrich, Carolina Alves Vestena, Florian Vietze, Marliese Weißmann, Holger Wittig-Koppe and Janina Zölch.
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Частини книг з теми "Michael's Addition"

1

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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2

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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3

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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4

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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5

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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6

Reetz, Manfred T. "Michael Additions." In Reactivity and Structure: Concepts in Organic Chemistry, 194–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70704-9_6.

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7

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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8

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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9

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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10

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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Тези доповідей конференцій з теми "Michael's Addition"

1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

Reznikov, A., D. Nikerov, and Yu Klimochkin. "ASYMMETRIC SYNTHESIS OF NEUROTROPIC DRUGS – GABA ANALOGS USING NI(II)-CATALYZED MICHAEL ADDITION." In MedChem-Russia 2021. 5-я Российская конференция по медицинской химии с международным участием «МедХим-Россия 2021». Издательство Волгоградского государственного медицинского университета, 2021. http://dx.doi.org/10.19163/medchemrussia2021-2021-31.

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10

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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