Relevant bibliographies by topics / Michael's Addition

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Michael's Addition'

Author: Grafiati
Published: 23 September 2022
Last updated: 31 July 2025

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Journal articles on the topic "Michael's Addition"

1

Thabet, H. Kh, Mohd Imran, Mohd Imran, Saleh Alaql, and M. H. M. Helal. "Bis(2-cyanoacetamide) in Heterocyclic Synthesis: Synthesis of Some Bis[2-oxopyridine, 2-iminochromene, Chromeno[3,4-c]pyridine, Benzochromeno[3,4-c]pyridine] Derivatives." Oriental Journal Of Chemistry 40, no. 1 (2024): 65–73. http://dx.doi.org/10.13005/ojc/400108.

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N,N'-(methylenebis(1,4-phenylene))bis-(2-cyanoacetamide) was exploited as a precursor for synthesing some bis (benzylidene 5a-c, pyridines 7, 8, 10a,b, chromene 14, benzochromene 15) derivatives containing diphenyl-methylene spacer via the reaction with each of aromatic aldehydes, pentane-2,4-dione, acetaldehyde/ malononitrile, arylidene-malononitriles, ethyl cinnamates, 2-hydroxybenzaldehyde, and 2-hydroxy-1-naphthaldehyde). Bis(chromeno[3,4-c]pyridines 16&18) were synthesized via Michael's addition of malononitrile or ethyl cyanoacetate to bis(chromene) derivative. The newly prepared com
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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 wi
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Perkasa Mega Dwiguna, I Ketut R Sudiarditha, and Corry Yohana. "THE The Effect Of Work Stress And Job Insecurity On Turnover Intention With Organizational Commitment As An Intervening At Pt "Xyz"." International Student Conference on Business, Education, Economics, Accounting, and Management (ISC-BEAM) 2, no. 1 (2024): 2345–59. http://dx.doi.org/10.21009/isc-beam.012.169.

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The role of employees as human resources is very crucial in the continuity of company operations. One of the main focuses in human resource management is employee turnover intention. This phenomenon can disrupt company stability and cause material and immaterial losses. Indonesia, according to data from Michael Page (2022), is ranked second highest in Asia Pacific in terms of employees' intention to resign. This research aims to identify the factors that influence turnover intention among PT "XYZ" employees and examine the influence of work stress and job insecurity on turnover intention with
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Hanna and Dwi Retno Widiyanti. "NIAT WAKAF TUNAI ONLINE PADA MAHASISWA EKONOMI ISLAM." Islamic Economics and finance in Focus 1, no. 4 (2022): 360–72. http://dx.doi.org/10.21776/ieff.2022.01.4.07.

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Indonesia with a majority Muslim community makes the potential for cash waqf very large. According to the National Committee for Islamic Economics and Finance (KNEKS), the potential for cash waqf could reach IDR 180 trillion, but the realization of waqf is still far below the existing potential. In general, the practice of waqf can help the socio-economic development of the Muslim community and distribute wealth among the community because waqf is intended to fund and maintain Islamic institutions such as madrasas, schools, universities and other public services. The research was conducted wit
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BOZKURT, Selahattin. "Asimetrik Michael Katılma Tepkimesi için Prolin bazlı β-Hidroksiamit Organokatalizörü". Afyon Kocatepe Üniversitesi Uluslararası Mühendislik Teknolojileri ve Uygulamalı Bilimler Dergisi 5, № 1 (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 a
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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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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 (2019): 18–22. http://dx.doi.org/10.23939/chcht13.01.018.

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A., S. Devi, C. Dutta M., Nongkhlaw R., and N. Vishwakarma J. "KHS04 assisted Michael addition-elimination reactions of formylated acetophenones in water : A facile general green synthetic route to 3-(alkyl/aralkyl/aryl)amino-1-arylprop-2-en-1-ones." Journal of Indian Chemical Society Vol. 87, Jun 2010 (2010): 739–42. https://doi.org/10.5281/zenodo.5791952.

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organic Research Lab., Department of Chemistry, St. Anthony&#39;s College. Shillong-793 001, Meghalaya. India <em>E-mail :</em> jnvishwakarma@rediffmail.com Fax : 91-0364-2229558 Department of Chemistry, North-Eastern Hill University, Shillong-793 022, Meghalaya&middot;. India <em>Manuscript received 18 August 2009, accepted 9 November 2009</em> A facile general green synthetic route to 3-(alkyl/aralkyl/aryl)amino-1-arylprop-2-en-1-ones in excellent yields has been developed by reacting formylated acetophenones with primary amines assisted by<strong> </strong>KHSO<sub>4</sub> in water.
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Liu, Zixuan. "Michael addition reaction and its examples." Applied and Computational Engineering 24, no. 6 (2023): 1–6. http://dx.doi.org/10.54254/2755-2721/24/ojs/20230669.

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Michael addition reaction refers to the conjugate addition reaction of carbocation to α, β-unsaturated aldehydes, ketones, carboxylic acids, esters, nitrile, nitro compounds, etc. The reaction is an essential organic reaction, and it is used in organic synthesis to grow carbon chains and synthesize organic compounds with various functional groups. As one of the most valuable organic synthesis reactions, it is one of the most common ways to construct carbon-carbon bonds. This paper analyzes the mechanisms and the theories of some common Michael addition reactions. It also includes an example of
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Liu, Zixuan. "Michael addition reaction and its examples." Applied and Computational Engineering 24, no. 1 (2023): 1–6. http://dx.doi.org/10.54254/2755-2721/24/20230669.

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Michael addition reaction refers to the conjugate addition reaction of carbocation to , -unsaturated aldehydes, ketones, carboxylic acids, esters, nitrile, nitro compounds, etc. The reaction is an essential organic reaction, and it is used in organic synthesis to grow carbon chains and synthesize organic compounds with various functional groups. As one of the most valuable organic synthesis reactions, it is one of the most common ways to construct carbon-carbon bonds. This paper analyzes the mechanisms and the theories of some common Michael addition reactions. It also includes an example of t
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Dissertations / Theses on the topic "Michael's Addition"

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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
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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 challen
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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.)<br>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 developme
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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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Jha, Sushil C. "Catalytic, enantioselective michael addition reaction." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2002. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2496.

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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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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 t
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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
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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 yie
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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
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Books on the topic "Michael's Addition"

1

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

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

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Pees, Klaus-Jürgen. Kohlenhydrate als chirale Matrizen in stereoselektiven Michael-Additionen. [s.n.], 1988.

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Aachen, Rheinisch-Westfälische Technische Hochschule, ed. Asymmetrische Synthese substituierter Cyclohexanone und Lignan-Lactone durch Michael-Addition mit lithiierten [alpha]-Aminonitrilen [Alpha-Aminonitrilen]. [s.n.], 1996.

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Latvala, Anita Sisko Kaarina. Asymmetrische Michael-Additionen: Strukturaufklärung der Amaryllidaceen-Alkaloide aus Galanthus elwesii Hooker fil. Zentralstelle der Studentenschaft, 1994.

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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. U.S. G.P.O., 1987.

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Mannes, Dietrich. Diastereo- und enantioselektive Synthese von 1,4-Diketonen durch Michael-Addition von chiralen [alpha]-Aminonitrilen [alpha-Aminonitrilen] an Enone. [s.n.], 1992.

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Rendenbach, Beatrice. Asymmetrische Michael-Additionen via SAMP-/RAMP-Hydrazone - diastereo- und enantioselektive Synthese von substituierten 5-Oxoestern [Oxoestern] und d-Lactonen [Delta-Lactonen]. [s.n.], 1987.

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United States. General Accounting Office. and United States Congress Senate, eds. United Nations: Early renovation planning reasonable, but additional management controls and oversight will be needed : report to the Honorable Michael Enzi, U.S. Senate. U.S. General Accounting Office, 2003.

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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 Heritage Trust, 2003.

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Book chapters on the topic "Michael's Addition"

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Li, Jie Jack. "Michael addition." In Name Reactions. 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. 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 Namensreaktionen. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-52850-7_93.

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

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

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Li, Jie Jack. "Mukaiyama Michael addition." In Name Reactions. 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 Namensreaktionen. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-52850-7_100.

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

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Conference papers on the topic "Michael's Addition"

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Tinsley, R. G. "Isocyanate Free Urethanes; a New Class of Coating System for Corrosion Resistant Finishes." In CORROSION 1994. NACE International, 1994. https://doi.org/10.5006/c1994-94600.

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Abstract As part of an ongoing effort to develop lower toxicity, more environmentally benign coatings binder systems, a series of polymers using a novel Michael Addition reaction cure mechanism, has been developed. For the cross-linking system, a number of lower molecular weight polymers with acceptor sites have been developed. They include in the polymer chain a significant amount of prereacted polyurethane, thereby giving the cured coating the familiar properties of a high quality standard polyurethane system. The chemistry of the cure mechanism is discussed pointing out the similarities and
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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. 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. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013820194343.

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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. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013819173959.

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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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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. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a045.

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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. 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. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013915204013.

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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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Reports on the topic "Michael's Addition"

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Gubalova, Vladislava, Lucia Rybnikarova, Gaspar Schnitzler, Edouard Simon, and Arto Väisänen. Analysing Political Acceptability of Reforms Among National Policymakers. EsadeGeo. Center for Global Economy and Geopolitics, 2022. https://doi.org/10.56269/202212vg.

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The EU finds itself facing serious security threats in an increasingly polarised global environment. Against this backdrop, it is necessary to explore the perceptions and preferences of Member States (MS) towards EU foreign and security policy. This paper, which bases itself on theoretical work conducted in ENGAGE Working Paper 2 (Michaels &amp; Kissack, 2021), aims to shed light on where various MS stand regarding a range of reforms and underused mechanisms by assessing levels of acceptability among national policymaking elites. Focusing on the main reform proposals under consideration, as we
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