Relevant bibliographies by topics / Coupling Reactions

Contents

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

Academic literature on the topic 'Coupling Reactions'

Author: Grafiati
Published: 4 June 2021
Last updated: 20 July 2024

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Coupling Reactions.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Coupling Reactions"

1

Pires, Marina, Sara Purificação, A. Santos, and M. Marques. "The Role of PEG on Pd- and Cu-Catalyzed Cross-Coupling Reactions." Synthesis 49, no. 11 (April 26, 2017): 2337–50. http://dx.doi.org/10.1055/s-0036-1589498.

Full text
Abstract:
Carbon–carbon and carbon–heteroatom coupling reactions are among the most important transformations in organic synthesis as they enable complex structures to be formed from readily available compounds under different routes and conditions. Several metal-catalyzed cross-coupling reactions have been developed creating many efficient methods accessible for the direct formation of new bonds between differently hybridized carbon atoms.During the last decade, much effort has been devoted towards improvement of the sustainability of these reactions, such as catalyst recovery and atom efficiency. Polyethylene glycol (PEG) can be used as a medium, as solid-liquid phase transfer catalyst, or even as a polymer support. PEG has been investigated in a wide variety of cross-coupling reactions either as an alternative solvent to the common organic solvents or as a support for catalyst, substrate, and ligand. In this review we will summarize the different roles of PEG in palladium- and copper-catalyzed cross-coupling reactions, with the focus on Heck, Suzuki–Miyaura, Sonogashira, Buchwald–Hartwig, Stille, Fukuyama, and homocoupling reactions. We will highlight the role of PEG, the preparation of PEGylated catalysts and substrates, and the importance for the reaction outcome and applicability.1 Introduction2 PEG in Heck Reactions3 PEG in Homocoupling Reactions4 PEG in Suzuki–Miyaura Reactions5 PEG in Sonogashira Reactions6 PEG in Buchwald–Hartwig Reactions7 PEG in Stille Reactions8 PEG in Fukuyama Reactions9 PEG in Miscellaneous Cross-Coupling Routes10 Conclusions
APA, Harvard, Vancouver, ISO, and other styles
2

Kumar, Anil, Saurav Kumar, Jyoti Jyoti, Deepak Gupta, and Gajendra Singh. "A Decade of Exploration of Transition-Metal-Catalyzed Cross-Coupling Reactions: An Overview." SynOpen 07, no. 04 (November 2023): 580–614. http://dx.doi.org/10.1055/s-0040-1720096.

Full text
Abstract:
AbstractDuring the previous couple of decades, transition-metal (Fe, Co, Cu, Ni, Ru, Rh, Pd, Ag, Au) catalyzed inter- and intramolecular coupling reactions have attracted huge attention for the construction of C–C and C–heteroatom (like C–N, C–P, C–O, C–S, etc.) bonds to synthesize a diverse range of polymers, fine chemicals, and agrochemicals (mainly fungicides, herbicides, and insecticides), as well as biologically and pharmaceutically important organic molecules. Furthermore, the employment of lower cost and easily available metals such as first-row transition-metal salts or metal complexes of Fe, Co, Cu, Ni as catalysts compared to the precious metals such as Pd, Ag, Au in cross-coupling reactions have led to major advances in applications within the fields of synthesis. A number of cross-coupling reactions catalyzed by transition metals have been explored, including Suzuki, Heck, Sonogashira, Stille, Kumada, Kochi, Murahashi, Corriu, and Negishi reactions, as well as carbonylative, decarboxylative, reactions and α-arylations. In this review, we offer a comprehensive summary of the cross-coupling reaction catalyzed by different transition metals from the year 2009 to date.1 Introduction2 Pd-Catalyzed Reactions2.1 C–C Cross-Coupling Reactions2.2 C–N Cross-Coupling Reactions2.3 C–P Cross-Coupling Reactions3 Ni-Catalyzed Cross-Coupling Reactions3.1 C–C Cross-Coupling Reactions4 Cu-Catalyzed Cross-Coupling Reactions4.1 C–C Cross-Coupling Reactions4.2 C–O Cross-Coupling Reactions4.2 C–N Cross-Coupling Reactions4.4 C–P Cross-Coupling Reactions4.5 C–Se Cross-Coupling Reactions4.6 C–S Cross-Coupling Reactions5 Fe-Catalyzed Reactions5.1 C–C Cross-Coupling Reactions5.2 C–S Cross-Coupling Reactions6 Co-Catalyzed Reactions7 Transition-Metal Nanoparticle-Promoted Reactions7.1 Pd Nanoparticles7.2 Cu Nanoparticles8 Miscellaneous Reactions9 Perspectives and Future Directions
APA, Harvard, Vancouver, ISO, and other styles
3

Kotha, Sambasivarao, Milind Meshram, and Nageswara Panguluri. "Advanced Approaches to Post-Assembly Modification of Peptides by Transition-Metal-Catalyzed Reactions." Synthesis 51, no. 09 (March 25, 2019): 1913–22. http://dx.doi.org/10.1055/s-0037-1612418.

Full text
Abstract:
We have summarized diverse synthetic approaches for the modification of peptides by employing transition-metal-catalyzed reactions. These methods can deliver unusual peptides suitable for peptidomimetics. To this end, several popular reactions such as Diels–Alder, 1,3-dipolar cycloaddition, [2+2+2] cyclotrimerization, metathesis, Suzuki­–Miyaura cross-coupling, and Negishi coupling have been used to assemble modified peptides by post-assembly chemical modification strategies.1 Introduction2 Synthesis of a Cyclic α-Amino Acid Derivative via a Ring-Closing Metathesis Protocol3 Peptide Modification Using a Ring-Closing Metathesis Strategy4 Peptide Modification via a [2+2+2] Cyclotrimerization Reaction5 Peptide Modification by Using [2+2+2] Cyclotrimerization and Suzuki Coupling6 Peptide Modification via a Suzuki–Miyaura Cross-Coupling7 Peptide Modification via Cross-Enyne Metathesis and a Diels–Alder­ Reaction as Key Steps8 Peptide Modification via 1,3-Dipolar Cycloaddition Reactions9 Modified Peptides via Negishi Coupling10 A Modified Dipeptide via Ethyl Isocyanoacetate11 Conclusions
APA, Harvard, Vancouver, ISO, and other styles
4

Daley, Ryan A., and Joseph J. Topczewski. "Aryl-Decarboxylation Reactions Catalyzed by Palladium: Scope and Mechanism." Synthesis 52, no. 03 (December 13, 2019): 365–77. http://dx.doi.org/10.1055/s-0039-1690769.

Full text
Abstract:
Palladium-catalyzed cross-couplings and related reactions have enabled many transformations essential to the synthesis of pharmaceuticals, agrochemicals, and organic materials. A related family of reactions that have received less attention are decarboxylative functionalization reactions. These reactions replace the preformed organometallic precursor (e.g., boronic acid or organostannane) with inexpensive and readily available carboxylic acids for many palladium-catalyzed reactions. This review focuses on catalyzed reactions where the elementary decarboxylation step is thought to occur at a palladium center. This review does not include decarboxylative reactions where decarboxylation is thought to be facilitated by a second metal (copper or silver) and is specifically limited to (hetero)arenecarboxylic acids. This review includes a discussion of oxidative Heck reactions, protodecarboxylation reactions, and cross-coupling reactions among others.1 Introduction2 Oxidative Heck Reactions3 Protodecarboxylation Reactions4 Cross-Coupling Reactions5 Other Reactions6 Conclusion
APA, Harvard, Vancouver, ISO, and other styles
5

Lee, Sunwoo, and Muhammad Aliyu Idris. "Recent Advances in Decarboxylative Reactions of Alkynoic Acids." Synthesis 52, no. 16 (April 6, 2020): 2277–98. http://dx.doi.org/10.1055/s-0040-1707600.

Full text
Abstract:
Alkynoic acids have been widely employed as alkyne and alkene sources in decarboxylative reactions. Alkynoic acid coupling leads to the formation of direct coupling products and cyclized products through sequential reactions. Moreover, homocoupling and multicomponent reactions have been developed. The decarboxylative addition of alkynoic acids generates the corresponding alkene products. A number of synthetic methods are utilized for the preparation of arylpropynoic acids including the Sonogashira coupling and the carboxylation of terminal alkynes. Recently, the use of decarboxylative halogenations has also been reported. This review covers decarboxylative reactions of alkynoic acids reported between 2013 and 2019; further, it is divided into several sections according to the type of reaction.1 Introduction2 Direct Coupling3 Sequential Reactions4 Homocoupling5 Multicomponent Reactions6 Addition7 Halogenations8 Synthesis of Alkynoic Acids9 Conclusion
APA, Harvard, Vancouver, ISO, and other styles
6

Koóš, Peter, Martin Markovič, Pavol Lopatka, and Tibor Gracza. "Recent Applications of Continuous Flow in Homogeneous Palladium Catalysis." Synthesis 52, no. 23 (August 3, 2020): 3511–29. http://dx.doi.org/10.1055/s-0040-1707212.

Full text
Abstract:
Considerable advances have been made using continuous flow chemistry as an enabling tool in organic synthesis. Consequently, the number of articles reporting continuous flow methods has increased significantly in recent years. This review covers the progress achieved in homogeneous palladium catalysis using continuous flow conditions over the last five years, including C–C/C–N cross-coupling reactions, carbonylations and reductive/oxidative transformations.1 Introduction2 C–C Cross-Coupling Reactions3 C–N Coupling Reactions4 Carbonylation Reactions5 Miscellaneous Reactions6 Key to Schematic Symbols7 Conclusion
APA, Harvard, Vancouver, ISO, and other styles
7

Nicholas, Kenneth M., and Chandrasekhar Bandari. "Deoxygenative Transition-Metal-Promoted Reductive Coupling and Cross-Coupling of Alcohols and Epoxides." Synthesis 53, no. 02 (October 7, 2020): 267–78. http://dx.doi.org/10.1055/s-0040-1707269.

Full text
Abstract:
AbstractThe prospective utilization of abundant, CO2-neutral, renewable feedstocks is driving the discovery and development of new reactions that refunctionalize oxygen-rich substrates such as alcohols and polyols through C–O bond activation. In this review, we highlight the development of transition-metal-promoted reactions of renewable alcohols and epoxides that result in carbon–carbon bond-formation. These include reductive self-coupling reactions and cross-coupling reactions of alcohols with alkenes and arene derivatives. Early approaches to reductive couplings employed stoichiometric amounts of low-valent transition-metal reagents to form the corresponding hydrocarbon dimers. More recently, the use of redox-active transition-metal catalysts together with a reductant has enhanced the practical applications and scope of the reductive coupling of alcohols. Inclusion of other reaction partners with alcohols such as unsaturated hydrocarbons and main-group organometallics has further expanded the diversity of carbon skeletons accessible and the potential for applications in chemical synthesis. Catalytic reductive coupling and cross-coupling reactions of epoxides are also highlighted. Mechanistic insights into the means of C–O activation and C–C bond formation, where available, are also highlighted.1 Introduction2 Stoichiometric Reductive Coupling of Alcohols3 Catalytic Reductive Coupling of Alcohols3.1 Heterogeneous Catalysis3.2 Homogeneous Catalysis4 Reductive Cross-Coupling of Alcohols4.1 Reductive Alkylation4.2 Reductive Addition to Olefins5 Epoxide Reductive Coupling Reactions6 Conclusions and Future Directions
APA, Harvard, Vancouver, ISO, and other styles
8

Akkarasamiyo, Sunisa, Somsak Ruchirawat, Poonsaksi Ploypradith, and Joseph S. M. Samec. "Transition-Metal-Catalyzed Suzuki–Miyaura-Type Cross-Coupling Reactions of π-Activated Alcohols." Synthesis 52, no. 05 (January 7, 2020): 645–59. http://dx.doi.org/10.1055/s-0039-1690740.

Full text
Abstract:
The Suzuki–Miyaura reaction is one of the most powerful tools for the formation of carbon–carbon bonds in organic synthesis. The utilization of alcohols in this powerful reaction is a challenging task. This short review covers progress in the transition-metal-catalyzed Suzuki­–Miyaura-type cross-coupling reaction of π-activated alcohol, such as aryl, benzylic, allylic, propargylic and allenic alcohols, between 2000 and June 2019.1 Introduction2 Suzuki–Miyaura Cross-Coupling Reactions of Aryl Alcohols2.1 One-Pot Reactions with Pre-activation of the C–O Bond2.1.1 Palladium Catalysis2.1.2 Nickel Catalysis2.2 Direct Activation of the C–O Bond2.2.1 Nickel Catalysis3 Suzuki–Miyaura-Type Cross-Coupling Reactions of Benzylic Alcohols4 Suzuki–Miyaura-Type Cross-Coupling Reactions of Allylic Alcohols4.1 Rhodium Catalysis4.2 Palladium Catalysis4.3 Nickel Catalysis4.4 Stereospecific Reactions4.5 Stereoselective Reactions4.6 Domino Reactions5 Suzuki–Miyaura-Type Cross-Coupling Reactions of Propargylic Alcohols5.1 Palladium Catalysis5.2 Rhodium Catalysis6 Suzuki–Miyaura-Type Cross-Coupling Reactions of Allenic Alcohols6.1 Palladium Catalysis6.2 Rhodium Catalysis7 Conclusions
APA, Harvard, Vancouver, ISO, and other styles
9

Morimoto, Koji, Toshifumi Dohi, and Yasuyuki Kita. "Metal-free Oxidative Cross-Coupling Reaction of Aromatic Compounds Containing Heteroatoms." Synlett 28, no. 14 (June 21, 2017): 1680–94. http://dx.doi.org/10.1055/s-0036-1588455.

Full text
Abstract:
The biaryl unit containing a heteroatom is a key structure in a large number of natural products and π-conjugated organic systems. The cross-couplings can provide powerful methods for the construction of biaryls and heterobiaryls; thus the development of a new coupling method has been intensively studied by synthetic chemists. Therefore, the oxidative biaryl coupling reaction of arenes containing a heteroatom is a significantly attractive, convenient, and straightforward route to the synthesis of biaryls due to its operational simplicity avoiding the preparation of the corresponding halogenated and metallated arenes. In this report, recent progress in the field of metal-free oxidative cross-coupling reactions of aromatic compounds using hypervalent iodine(III) reagents, is presented.1 Introduction2 Cyanation and Halogenation Reactions of Heteroaromatic Compounds3 Biaryl Coupling Reaction of Heteroaromatic Compounds3.1 Regioselective Coupling Reaction of Thiophenes3.2 Cross-Coupling Reaction of Thiophenes3.3 Coupling Reaction of EDOT and Pyrroles3.4 Cross-Coupling Reaction of Pyrroles4 Cross-Coupling Reaction of Anilines5 Cross-Coupling Reaction of Phenols6 Cross-Coupling Reaction of N-Heteroaromatics with Aryl Radicals from Diaryliodonium(III) Salts7 Conclusion
APA, Harvard, Vancouver, ISO, and other styles
10

Wang, Lei, Jincan Yan, Pinhua Li, Min Wang, and Caina Su. "The effects of amines on oxidative homo-coupling of terminal alkynes promoted by copper salts." Journal of Chemical Research 2005, no. 2 (February 2005): 112–15. http://dx.doi.org/10.3184/0308234054497083.

Full text
Abstract:
The effects of all kinds of amines on homo-couplings (Glaser reactions) of terminal alkynes promoted by copper salts and the Sonogashira coupling reactions were studied systematically. Diethylamine (2° amine) can serve as an excellent solvent, base and coordination ligand in the oxidative homo-coupling of terminal alkynes and several modified Glaser coupling procedures have been developed which are based on a catalytic amount of cuprous salts (CuI, CuBr or CuCl) with diethylamine systems. Homo-coupling of terminal acetylenes in the Sonogashira reaction could be inhibited by using triethylamine (3° amine) as reaction medium, and the cross-coupling products were formed as the exclusive products.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Coupling Reactions"

1

Lindh, Jonas. "Palladium(II)-Catalyzed Coupling Reactions." Doctoral thesis, Uppsala universitet, Avdelningen för organisk farmaceutisk kemi, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-130031.

Full text
Abstract:
Sustainable chemical processes are becoming increasingly important in all fields of synthetic chemistry. Catalysis can play an important role in developing environmentally benign chemical processes, and transition metals have an important role to play in the area of green chemistry. In particular, palladium(II) catalysis includes many key features for successful green chemistry methods, as demonstrated by a number of eco-friendly oxidation reactions catalyzed by palladium(II). The aim of the work presented in this thesis was to develop novel and greener palladium(II)-catalyzed coupling reactions. In striving to achieve this aim, the first open-vessel, room-temperature palladium(II)-catalyzed oxidative Heck reaction, using oxygen from the air as the reoxidant of palladium, was developed. In a further investigation of the palladium(II)-catalyzed oxidative Heck reaction, base-free conditions for the transformation were identified and suitable conditions for microwave-assisted oxidative Heck reactions were established. A convenient and low-cost palladium(II)-catalyzed method for the synthesis of styrene derivatives, by coupling arylboranes with vinyl acetate, was developed. The reaction mechanism was studied using ESI-MS, which enabled the detection of cationic palladium intermediates in ongoing productive reactions, and a plausible catalytic cycle was proposed. In an attempt to make the oxidative Heck and the styrene synthesis reactions more attractive from an industrial point of view, conditions for continuous flow synthesis were identified. The results were generally good and rapid synthesis of the desired products was obtained. The first palladium(II)-catalyzed C–P bond-forming Hirao-type reaction, employing arylboranes instead of the commonly used aryl halides, was developed. An ESI-MS study was performed, and a plausible catalytic pathway was suggested. Finally, a novel method for synthesizing aryl ketones from benzoic acids and nitriles, via palladium(II)-catalyzed decarboxylation of the benzoic acids, was established. Further, the reaction mechanism was studied by ESI-MS and a plausible catalytic route presented.
APA, Harvard, Vancouver, ISO, and other styles
2

Arismendi, Romero Graciela. "Paladium catalized cross-coupling reactions." Revista de Química, 2012. http://repositorio.pucp.edu.pe/index/handle/123456789/101014.

Full text
Abstract:
El premio Nobel en Química de este año ha sido otorgado a los investigadores Richard Heck (EE.UU.), Ei-ichi Negishi (EE.UU.) y Akira Suzuki (Japón), por sus valiosos aportesen el desarrollo de un tipo específico de reacciones para la formación de enlaces C-C: “Reacciones de acoplamientocruzado catalizadas por paladio”. La creciente demanda de nuevas sustancias para el desarrollo de medicamentos, materiales y/o compuestos biológicamente activos ha hecho de este descubrimiento una importante herramienta para los químicos, dándoles la capacidad de atender estas necesidades con la creación de moléculas complejas de utilidad industrial.
This year´s Nobel Prize in Chemistry has been awarded to the researchers Richard Heck (USA), Ei-Ichi Negishi(USA) and Akira Suzuki (Japan), for their valuable contributions to the development of a specific type of reaction for the formation of carbon-carbon bonds: “Palladium-catalyzed cross couplings”. The growing demand for new substances for drug development, materials and/or biologically active compounds has made this discovery an important tool for chemists, giving them the ability to meet these needs through the creation of complex molecules of industrial utility.
APA, Harvard, Vancouver, ISO, and other styles
3

Hill, J. "Non-aqueous diazotisation, diazo coupling and triphase diazo coupling reactions." Thesis, University of Leeds, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355948.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Thathagar, Mehul Bhupendra. "Nanocluster catalysed C-C coupling reactions." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2006. http://dare.uva.nl/document/18448.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Pyatt, D. "Organic synthesis via palladium coupling reactions." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.257950.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Collings, M. P. "Alkyne coupling reactions on palladium catalysts." Thesis, University of Cambridge, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.597856.

Full text
Abstract:
The chemistry of the simple alkyne compounds ethyne (acetylene), propyne (methylacetylene) and 2-butyne (dimethylacetylene) over various palladium catalysts has been studied. Both UHV experiments with single crystal surfaces and microreactor experiments with zeolite supported palladium clusters were performed. A particular emphasis was placed on coupling reactions - the bonding of two or more alkyne molecules. The adsorption and chemistry of propyne on Pd(111) and Au/Pd(111) alloy surfaces has been studied in detail using XPS, AES, LEED, UPS and TDS. Close reference to is made to the chemistry of ethyne on these surfaces, which has been previously investigated. The adsorption configuration of propyne closely resembles that of ethyne. Molecular desorption of propyne is the most efficient process, although coupling to benzene, hydrogenation of propene and decomposition represent significant reaction pathways. Cyclotrimerisation of propyne to trimethylbenzene is activated over Au/Pd(111), but the efficiency of this reaction is much lower than the analogous reaction of ethyne. A less detailed investigation of 2-butyne chemistry provided further comparative data. The adsorption configuration adopted by 2-butyne is more distorted than that of ethyne and propyne. 2-butyne is inactive for coupling on both Pd(111) and Au/Pd(111) alloys. The formation of toluene and xylene by mixed coupling reactions of various combinations of ethyne, propyne and 2-butyne was observed over Au/Pd(111). Formation of tetramethylbenzene and larger methyl benzene products was not observed. Several possible heterocyclic coupling reactions of propyne were investigated, but of these, only the addition of oxygen to form dimethylfuran was observed.
APA, Harvard, Vancouver, ISO, and other styles
7

Ji, Jianhua. "Regioselective Coupling Reactions of Diiodophenol Derivatives." Thesis, University of North Texas, 1994. https://digital.library.unt.edu/ark:/67531/metadc277926/.

Full text
Abstract:
Palladium catalyzed reactions of derivatives of 2,4-diiodophenol are explored. Coupling reactions with a series of terminal alkynes and formylation are found to be efficient and regioselective. Coupling with stananne reagents and alkenes do not work. The nature of the oxygen protecting group is critical. The phytotoxic natural product, Eutypine, is synthesized by using regioselective formylation and alkyne coupling. An approach to the plant antimicrobial compound Plicatin B is examined.
APA, Harvard, Vancouver, ISO, and other styles
8

Rodrigo, Sanjeewa K. "Nickel Catalyzed Regioselective Reductive Coupling Reactions." University of Cincinnati / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Hua, Xi Ye. "Expanding the Scope of Coupling Partners in Catalytic Cross-Coupling Reactions." Thesis, Université d'Ottawa / University of Ottawa, 2016. http://hdl.handle.net/10393/35521.

Full text
Abstract:
Carbon-carbon (C-C) bond formation is among the most important processes in organic chemistry. Transition metal catalyzed C-C bond formation is an active research area that shows great potential due to high selectivity and relatively mild conditions. In Chapter 1, a new reaction for direct acylation of aryl halides is discussed. Specifically, the catalytic reaction between aryl halides/pseudohalides and aldehydes is explored. The choice of ligand, base, solvent, temperature, catalyst and substrates are important factors for optimizing this catalytic reaction. The various combinations of all these factors have, therefore, been examined by high-throughput screening (HTS) in order to develop the new C-C coupling reaction. In Chapter 2, a new methodology is reported in order to expand the scope of the Kumada-Corriu cross-coupling reaction. The strategy to achieve this goal is mechanistically based, matching oxidative addition rates with the rate of syringe pump addition of the Grignard to minimize the exposure of sensitive groups to the aggressive nucleophile. Aryl chlorides containing esters, amides, nitriles, pyrazines, carbamates, ketones, and other sensitive functionalities are all demonstrated to undergo chemoselective cross-coupling with this technique. The mechanistic reason for the effectiveness of this strategy is uncovered by continuous-infusion ESI-MS studies.
APA, Harvard, Vancouver, ISO, and other styles
10

Karpov, Alexei S. "Multi-component reactions initiated via Sonogashira coupling." [S.l. : s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=974467197.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Coupling Reactions"

1

Miyaura, Norio, ed. Cross-Coupling Reactions. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45313-x.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Nishihara, Yasushi, ed. Applied Cross-Coupling Reactions. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32368-3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Lei, Aiwen, Wei Shi, Chao Liu, Wei Liu, Hua Zhang, and Chuan He. Oxidative Cross-Coupling Reactions. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527680986.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Molnár, Árpád, ed. Palladium-Catalyzed Coupling Reactions. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648283.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Diederich, François, and Peter J. Stang, eds. Metal-Catalyzed Cross-Coupling Reactions. Weinheim, Germany: Wiley-VCH Verlag GmbH, 1998. http://dx.doi.org/10.1002/9783527612222.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Evano, Gwilherm, and Nicolas Blanchard, eds. Copper-Mediated Cross-Coupling Reactions. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118690659.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Diederich, François. Metal-catalyzed cross-coupling reactions. New York: Wiley-VCH, 1998.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

N, Diederich François, and Stang P. J, eds. Metal-catalyzed cross-coupling reactions. 2nd ed. Weinheim: Wiley-VCH, 2004.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

de, Meijere A., and Diederich François, eds. Metal-catalyzed cross-coupling reactions. 2nd ed. Weinheim: Wiley-VCH, 2004.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

Ligand coupling reactions with heteroatomic compounds. New York: Pergamon, 1998.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Coupling Reactions"

1

Gras, J. L. "Coupling Reactions." In Inorganic Reactions and Methods, 205–6. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145319.ch64.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Li, Jie Jack. "Glaser coupling." In Name Reactions, 160. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_122.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Li, Jie Jack. "McMurry coupling." In Name Reactions, 244. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_181.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Li, Jie Jack. "Stille coupling." In Name Reactions, 393. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_288.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Li, Jie Jack. "Suzuki coupling." In Name Reactions, 401. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_294.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Li, Jie Jack. "Glaser coupling." In Name Reactions, 282–86. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_119.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Li, Jie Jack. "McMurry coupling." In Name Reactions, 370–71. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_160.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Li, Jie Jack. "Stille coupling." In Name Reactions, 584–85. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_264.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Li, Jie Jack. "Ullmann coupling." In Name Reactions, 611–12. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_277.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Li, Jie Jack. "Glaser coupling." In Name Reactions, 142. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_114.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Coupling Reactions"

1

Kawano, T., L. Bonneau, and A. K. Kerman. "Effects of direct reaction coupling in compound reactions." In International Conference on Nuclear Data for Science and Technology. Les Ulis, France: EDP Sciences, 2007. http://dx.doi.org/10.1051/ndata:07455.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Trimper, Steffen. "Feedback Coupling and Chemical Reactions." In SLOW DYNAMICS IN COMPLEX SYSTEMS: 3rd International Symposium on Slow Dynamics in Complex Systems. AIP, 2004. http://dx.doi.org/10.1063/1.1764187.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Čapek, Petr, Miroslav Otmar, Milena Masojídková, and Antonín Holý. "Cross-coupling reactions of 2,6-dichloro-9-deazapurine." In XIIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2002. http://dx.doi.org/10.1135/css200205304.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Nunes, F. M., and A. Mukhamedzhanov. "Coupling in transfer reactions and the ANC method." In NUCLEAR PHYSICS IN THE 21st CENTURY:International Nuclear Physics Conference INPC 2001. AIP, 2002. http://dx.doi.org/10.1063/1.1469967.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Chang, S. L., S. A. Lottes, C. Q. Zhou, and M. Petrick. "A Hybrid Technique for Coupling Chemical Kinetics and Hydrodynamics Computations in Multi-Phase Reacting Flow Systems." In ASME 1997 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1997. http://dx.doi.org/10.1115/imece1997-0877.

Full text
Abstract:
Abstract A hybrid technique to couple hydrodynamics and chemical kinetics calculations in a multi-phase, multi-species, turbulent reacting flow simulation has been developed. It divides a flow simulation into two parts: a reacting flow hydrodynamic simulation with a small but sufficient number of lumped reactions to compute flow field properties followed by a many subspecies (of order 10 to 100) reaction kinetics and transport calculation. This technique has been incorporated in a computational fluid dynamics (CFD) code to predict concentrations of many subspecies in a reacting flow where complex chemical reactions take place, and it can be applied to many applications such as combustors. The application presented in this paper is the flow simulation of a fluid catalytic cracking (FCC) riser reactor. Applying the technique in the FCC riser application has shown that it can be used to identify critical processes and operating parameters including the trends and relationships that are necessary to the improve the quality and quantity of FCC products.
APA, Harvard, Vancouver, ISO, and other styles
6

Lima, Lucas Welington, and Ataualpa A. C. Braga. "Computational study on the reaction mechanism of Cp*Rh(III)-catalyzed cross-coupling reactions." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol2020144.

Full text
Abstract:
The reaction mechanism of reaction reported by Onodera et al4 was studied in the M06L/Def2SVP level of theory. Two possible reaction products were characterized, named as product a and product b, where product a that was identified in the experimental study is due to a exergonic reaction and product b due to a endoergonic reaction.
APA, Harvard, Vancouver, ISO, and other styles
7

Carvalho, Diego B., Camila B. Andrade, Carla R. Z. Miranda, Gabriela R. Hurtado, Luiz H. Viana, Palimécio G. Guerrero Jr., and Adriano C. M. Baroni. "Synthesis of Thiophene Acetylenes via Sonogashira Cross- Coupling Reactions." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013820103940.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Gobo, Nicholas R. S., Timothy J. Brocksom, and Kleber T. de Oliveira. "Cross-coupling reactions as a strategy for Naphthalocyanine synthesis." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013911161227.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Wang, Dawei, Rajesh Patel, Chao Zhu, and Teh C. Ho. "Coupling of Hydrodynamics, Vaporization and Reaction With Liquid Spray Injection Into a High-Temperature Gas-Solid Reactor." In ASME/JSME 2011 8th Thermal Engineering Joint Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/ajtec2011-44158.

Full text
Abstract:
A mechanistic model that to provide a quantitative understanding of the interplay of hydrodynamics, heat/mass transfer, and cracking reactions in the feed injection zone of a fluid catalytic cracking (FCC) riser reactor with a single nozzle spray. With the injection of an oil spray into a gas-solid flow, the collision between cold oil droplets and hot catalyst particles results in a strong momentum transfer that affects the spray hydrodynamics in terms of penetration and scattering. It also causes a significant heat transfer giving rise to rapid droplet vaporization and the attendant cooling of the catalyst. The presence of cracking reactions introduces volume expansion, changes in gas composition and volume fraction, and a cooling effect due to endothermicity. Accordingly, we in this study present an analysis of chemically-induced “entrance effects” in an FCC riser with a single nozzle spray. The cracking reaction network is described by a four-lump reaction model, while the ambient gas-solid transport is represented by a dense-phase riser flow. A Lagrangian modeling approach is adopted to track the spray trajectory as cracking reactions proceed. It is shown that cracking reactions play an important role in dictating the spray behavior, reaction and heat/mass transfer characteristics in the feed injection zone of an FCC riser.
APA, Harvard, Vancouver, ISO, and other styles
10

Sun, Jian, Zhaohui Jin, Ning Xie, Hong Wang, and Huajing Gao. "STUDIES ON SUZUKI COUPLING REACTIONS OF LARGE STERICALLY HINDERED SUBSTRATES." In International Conference on New Materials and Intelligent Manufacturing. Volkson Press, 2018. http://dx.doi.org/10.26480/icnmim.01.2018.24.26.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Coupling Reactions"

1

Bedi, Vaibhav, Puja K. Mahajan, and Nitin T. Patil. Gold Catalysis: A New Contender for Cross-Coupling Reactions with Aryl Halides. The Israel Chemical Society, March 2023. http://dx.doi.org/10.51167/acm00038.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Heinemann, H., G. A. Somorjai, and D. L. Perry. Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Office of Scientific and Technical Information (OSTI), March 1992. http://dx.doi.org/10.2172/7152421.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Heinemann, H., G. A. Somorjai, and D. L. Perry. Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, October 1--December 31, 1992. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/10160558.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Heinemann, H., G. A. Somorjai, and D. L. Perry. Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, July 1--September 30, 1992. Office of Scientific and Technical Information (OSTI), September 1992. http://dx.doi.org/10.2172/10163938.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Iglesia, E., H. Heinemann, and D. L. Perry. Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, 1 January--31 March 1994. Office of Scientific and Technical Information (OSTI), March 1994. http://dx.doi.org/10.2172/10165399.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Heinemann, H., G. A. Somorjai, and D. L. Perry. Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, January 1--March 31, 1992. Office of Scientific and Technical Information (OSTI), March 1992. http://dx.doi.org/10.2172/10178973.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Heinemann, H., E. Iglesia, and D. L. Perry. Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, October 1--December 31, 1993. Office of Scientific and Technical Information (OSTI), December 1993. http://dx.doi.org/10.2172/10129151.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Heinemann, H., G. A. Somorjai, and D. L. Perry. Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, April 1, 1992--June 30, 1992. Office of Scientific and Technical Information (OSTI), June 1992. http://dx.doi.org/10.2172/10161650.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Heinemann, H., G. A. Somorjai, and D. L. Perry. Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, January 1, 1993--March 31, 1993. Office of Scientific and Technical Information (OSTI), March 1993. http://dx.doi.org/10.2172/10163179.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Heinemann, H., G. A. Somorjai, and D. L. Perry. Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, July 1, 1993--September 30, 1993. Office of Scientific and Technical Information (OSTI), November 1993. http://dx.doi.org/10.2172/10192478.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Coupling Reactions' for particular source types:
Journal articles Dissertations / Theses Books
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography