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Relevant bibliographies by topics / Suzuki Coupling Reaction

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Academic literature on the topic 'Suzuki Coupling Reaction'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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Journal articles on the topic "Suzuki Coupling Reaction"

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

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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 Modificati

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

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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

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Len, Christophe. "Catalysts for Suzuki–Miyaura Coupling Reaction." Catalysts 10, no. 1 (2020): 50. http://dx.doi.org/10.3390/catal10010050.

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Bhatt, Nikita, Smriti, Richa Khare, and Monika Kamboj. "Suzuki-Miyaura Cross Coupling Reaction in Various Green Media." Asian Journal of Chemistry 33, no. 9 (2021): 1976–84. http://dx.doi.org/10.14233/ajchem.2021.22584.

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Suzuki-Miyaura cross-coupling reaction is an efficient and utilized method for the direct formation of carbon-carbon bonds. The effectiveness and efficiency of Suzuki-Miyaura cross-coupling reaction and its applications have been the topic of interest for synthetic chemists for the last few decades. Green chemistry is the area where we use eco-friendly products. Suzuki coupling includes palladium or nickel catalyzed coupling reaction, which involves ester of boric acids or simply boric acids with the organic halides or pseudohalide. In recent years, these catalytic systems have been developed

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Franzén, Robert, and Youjun Xu. "Review on green chemistry Suzuki cross coupling in aqueous media." Canadian Journal of Chemistry 83, no. 3 (2005): 266–72. http://dx.doi.org/10.1139/v05-048.

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The Suzuki cross-coupling reaction is a very efficient, reliable, and environmentally friendly method for the introduction of novel carboncarbon bonds into molecules. This review summarizes recent advances in the use of the reaction in aqueous media with a focus on different types of ligands and the ligandless protocols currently in use. Several synthetic targets for the reaction have been mentioned. The work summarizes recent results from studies on asymmetric Suzuki reactions performed in organic aqueous mixed solvents.Key words: Suzuki reaction, green chemistry, metal-catalyzed cross-cou

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Rocard, Lou, and Piétrick Hudhomme. "Recent Developments in the Suzuki–Miyaura Reaction Using Nitroarenes as Electrophilic Coupling Reagents." Catalysts 9, no. 3 (2019): 213. http://dx.doi.org/10.3390/catal9030213.

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Palladium-catalyzed cross-coupling reactions are nowadays essential in organic synthesis for the construction of C–C, C–N, C–O, and other C-heteroatom bonds. The 2010 Nobel Prize in Chemistry to Richard F. Heck, Ei-ichi Negishi, and Akira Suzuki was awarded for the discovery of these reactions. These great advances for organic chemists stimulated intense research efforts worldwide dedicated to studying these reactions. Among them, the Suzuki–Miyaura coupling (SMC) reaction, which usually involves an organoboron reagent and an organic halide or triflate in the presence of a base and a palladium

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Snieckus, Victor, and Claude Quesnelle. "The Directed ortho Metalation (DoM)–Cross-Coupling Connection: Synthesis of Polyfunctional Biaryls." Synthesis 50, no. 22 (2018): 4413–28. http://dx.doi.org/10.1055/s-0037-1610273.

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A comparative evaluation of the combined directed ortho metalation (DoM)–Suzuki–Miyaura and DoM–Negishi cross-coupling reactions with aryl triflates for the synthesis of substituted biaryls is described. Both ortho-zinc and ortho-boron aryl directed metalation group (DMG = CON(i-Pr)2, OCONEt2, OMOM, NHBoc) substrates were evaluated. The superiority of the DoM–Negishi over the DoM–Suzuki–Miyaura reaction in operational convenience and mild reaction conditions is noted. Orthogonal Negishi and Suzuki–Miyaura with Corriu–Kumada reactions for the synthesis of a teraryl derivative is also reported.

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Vaaland, Ingrid Caroline, and Magne Olav Sydnes. "Consecutive Palladium Catalyzed Reactions in One-Pot Reactions." Mini-Reviews in Organic Chemistry 17, no. 5 (2020): 559–69. http://dx.doi.org/10.2174/1570193x16666190716150048.

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Combining palladium catalyzed reactions in one-pot reactions represents an efficient and economical use of catalyst. The Suzuki-Miyaura cross-coupling has been proven to be a reaction which can be combined with other palladium catalyzed reactions in the same pot. This mini-review will highlight some of the latest examples where Suzuki-Miyaura cross-coupling reactions have been combined with other palladium catalyzed reactions in one-pot reaction. Predominantly, examples with homogeneous reaction conditions will be discussed in addition to a few examples from the authors where Pd/C have been us

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Friesen, Richard W., and Laird A. Trimble. "Comparison of the Suzuki cross-coupling reactions of 4,7-dichloroquinoline and 7-chloro-4-iodoquinoline with arylboronic acids using phosphine-free palladium catalysis in water." Canadian Journal of Chemistry 82, no. 2 (2004): 206–14. http://dx.doi.org/10.1139/v03-187.

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4,7-Dichloroquinoline (1a) and 7-chloro-4-iodoquinoline (1b) undergo Suzuki cross-coupling reactions with arylboronic acids catalyzed by phosphine-free palladium acetate in boiling water. Using phenylboronic acid (2), the reaction of 1a provides 7-chloro-4-phenylquinoline (3) (78%) together with diphenylquinoline (4) (12%), while 1b reacts in a much more regioselective fashion and provides 3 in 98% isolated yield. Although 1b undergoes a more regioselective Suzuki reaction than 1a, additional important observations are that the overall reaction of 1b with 2 is three times slower than 1a and th

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Gujral, Sarbjeet Singh, Smriti Khatri, Poornima Riyal, and Vinod Gahlot. "ChemInform Abstract: Suzuki Cross-Coupling Reaction." ChemInform 44, no. 32 (2013): no. http://dx.doi.org/10.1002/chin.201332262.

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Dissertations / Theses on the topic "Suzuki Coupling Reaction"

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Daku, Kokovi Lawson. "Applications of the Suzuki cross coupling reaction." Thesis, University of Bath, 2003. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.425882.

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Hashimoto, Toru. "Development of Iron-Catalyzed Suzuki-Miyaura Coupling Reaction." 京都大学 (Kyoto University), 2012. http://hdl.handle.net/2433/159407.

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Kuvayskaya, Anastasia, and Aleksey Vasiliev. "Use of Suzuki Coupling Reaction for Synthesis of Functionalized Materials." Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/asrf/2019/schedule/162.

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Hybrid materials synthesized by grafting of organic molecules onto silica surface have found numerous applications in chemistry, biochemistry, and chemical engineering. In particular, the functionalization of silica gel can be accomplished by various surface reactions of immobilized boronic acids. Suzuki coupling has been chosen due to several advantages, such as mild reaction conditions, tolerance to the aqueous environment, and high yields of the products. The objective of this work was to determine the most effective reaction conditions for modifying porous hybrid materials with large speci

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Geogheghan, Katherine Jayne. "Boronic acid speciation in Suzuki-Miyaura cross-coupling." Thesis, University of Edinburgh, 2018. http://hdl.handle.net/1842/33092.

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Since its discovery in 1979, the Suzuki-Miyaura (SM) reaction has become one of the most widely utilised tools for carbon-carbon bond formation. The palladium catalysed coupling of an organoboron and organohalide compounds proceeds through a three-stage mechanism of oxidative addition, transmetalation and reductive elimination. The transmetalation of boronic acids to a palladium(II) complex has been widely studied. However, very little is known about the transmetalation of boronic esters, which are commonly used as an alternative to unstable boronic acids. Whether these species undergo direct

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Heaner, William. "Indole synthesis: Knoevenagel/Hemetsberger reaction sequence; Suzuki coupling reactions of basic nitrogen containing substrates." Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/52171.

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A series of substituted indoles have been synthesized by the sequential reaction of aromatic aldehydes with ethyl azidoacetate in the presence of sodium ethoxide to form the corresponding ethyl α-azido-β-arylacrylates (Knoevenagel process) followed by a solvent mediated thermolysis (Hemetsberger process). The isolated yields of the ethyl α-azido-β-arylacrylates were significantly increased when employing the sacrificial electrophile ethyl trifluoroacetate. 1H NMR and coupled 1H-13C NMR analysis of the ethyl α-azido-β-arylacrylates indicate that the condensation is stereospecific—only the Z

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Hassanzadeh, Nazanin. "Suzuki reactions in novel liquids." Thesis, Linnéuniversitetet, Institutionen för kemi och biomedicin (KOB), 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-106739.

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Non-ionic deep eutectic solvent (ni-DES) possesses various advantages such as good solvation, biodegradability, and non-toxicity which makes it a perfect and environmentally friendly solvent for organic synthesis. A Pd (OAc)2 catalyzed, Suzuki reaction of aryl bromide and N-heteroaryl halide with arylboronic acid in green and novel solvent (ni-DES) is described. In this work, the possibility of using ni-DES and the impact of this solvent on the scope of the reaction is studied. It is illustrated that using the mixture of N-alkyl derivatives of urea and acetamide as a green solvent for Suzuki r

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Chang, Weng Kun. "Development of Tandem Reaction for Synthesis of Highly Functionalized Carbocycles." Thesis, Boston College, 2014. http://hdl.handle.net/2345/bc-ir:104067.

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Thesis advisor: James P. Morken<br>The Suzuki-Miyaura cross-coupling reaction is a common strategy for the formation of a new carbon-carbon bond in organic synthesis. However, intramolecular coupling of allylboron ester and aryl electrophiles has never been reported. Herein, Pd-catalyzed intramolecular cross-coupling of allylboronic pinacol ester and vinyl or aryl bromides is presented. Pt-catalyzed 1,2-diboration of 1,3-dienes give α-chiral bis-allylboronic esters, which can undergo diastereoselective additions to carbonyl electrophiles tethered to vinyl or aryl halides to generate a new ally

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Watts, Nicola Louisa. "Improving the scope and understanding of the Symmetric and Asymmetric Suzuki coupling reaction." Thesis, University of East Anglia, 2012. https://ueaeprints.uea.ac.uk/48116/.

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Investigations into the Symmetric and Asymmetric Suzuki cross-coupling reaction have been described. A new reaction protocol has been developed in which isolated pre-activated sodium trihydroxyarylborate salts were employed as the organoboron coupling partner, resulting in a more convenient and stoichiometrically efficient process. This alternative protocol has been applied to symmetric Suzuki reactions employing simple electron-rich and electron-poor aryl halide partners, and to sterically challenging Suzuki reactions employing bulkier substrates. Asymmetric (atroposelective) Suzuki coupling

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Crepy, Karen Viviane Lucile. "A new asymmetric aryl-aryl coupling reaction and its application to the synthesis of novel liquid crystals." Thesis, University of East Anglia, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327498.

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Paris, Juraj [Verfasser]. "Combination of Suzuki cross-coupling reaction and biocatalysis in one-pot cascade processes / Juraj Paris." Bielefeld : Universitätsbibliothek Bielefeld, 2019. http://d-nb.info/1206592222/34.

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Books on the topic "Suzuki Coupling Reaction"

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Suzuki–Miyaura Cross-Coupling Reaction and Potential Applications. MDPI, 2017. http://dx.doi.org/10.3390/books978-3-03842-557-1.

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Book chapters on the topic "Suzuki Coupling Reaction"

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García Melchor, Max. "An Asymmetric Suzuki-Miyaura Reaction Mechanism." In A Theoretical Study of Pd-Catalyzed C-C Cross-Coupling Reactions. Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01490-6_6.

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Roy, Moumita, Pravin R. Likhar, and M. Lakshmi Kantam. "Polyaniline-Immobilized Palladium for Suzuki-Miyaura Coupling Reaction in Water." In Solid-Phase Organic Syntheses. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118336953.ch9.

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Li, Jie Jack. "Suzuki coupling." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_282.

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

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Li, Jie Jack. "Suzuki–Miyaura coupling." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_250.

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Li, Jie Jack. "Suzuki–Miyaura coupling." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_269.

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Li, Jie Jack. "Suzuki–Miyaura Coupling." In Name Reactions. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_147.

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Abreu, Ana S., Paula M. T. Ferreira, Maria-João R. P. Queiroz, et al. "Suzuki Coupling Reactions." In Catalysts for Fine Chemical Synthesis, Volume 3, Metal Catalysed Carbon-Carbon Bond-Forming Reactions. John Wiley & Sons, Ltd, 2005. http://dx.doi.org/10.1002/0470862017.ch4.

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Rossi, Liane M., Natalia J. S. Costa, Jones Limberger, and Adriano L. Monteiro. "Nanocatalysts for the Suzuki Coupling Reactions." In Nanocatalysis Synthesis and Applications. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118609811.ch3.

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Sun, Ho-Yan, and Dennis G. Hall. "At the Forefront of the Suzuki–Miyaura Reaction: Advances in Stereoselective Cross-Couplings." In Synthesis and Application of Organoboron Compounds. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-13054-5_7.

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Conference papers on the topic "Suzuki Coupling Reaction"

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Lee, Tae-Kyung, Bikashý Manandhar, and Jung-Mo Ahn. "Peptide Ligation via Suzuki-Miyaura Cross-Coupling Reaction." In The 24th American Peptide Symposium. Prompt Scientific Publishing, 2015. http://dx.doi.org/10.17952/24aps.2015.268.

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Tran, Thanh-Dao, and Haeil Park. "Application of Suzuki Coupling Reaction for Preparation of Some Arylchrysin Analogues." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01227.

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Liu, Yang, and Xue-Feng Bai. "Air Glow Discharge Plasma Reduction to Synthesize Pd/C Catalyst for Suzuki Coupling Reaction." In The 2nd Annual International Workshop on Materials Science and Engineering (IWMSE 2016). WORLD SCIENTIFIC, 2017. http://dx.doi.org/10.1142/9789813226517_0042.

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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.

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"Convenient and Efficient Suzuki Miyaura Coupling Reactions of Meso-Halogenated BODIPYs." In Chemical technology and engineering. Lviv Polytechnic National University, 2021. http://dx.doi.org/10.23939/cte2021.01.184.

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Thiemann, Thies, and Kyoko Yamamoto. "Suzuki-Miyaura cross-coupling and Heck reactions catalysed by Pd on carbon nanofibres." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00173.

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da Silva, A. J. M., C. Schneider, and V. Snieckus. "Construction of Polyarylated Fluorenones via chemoselective Ru- and Pd-Catalyzed Suzuki Cross-Coupling Reactions." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0007-1.

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Thiemann, Thies, Christian Burmester, Kodai Shiine, and Shuntaro Mataka. "From Suzuki-Miyaura cross coupling reactions of 2-bromo- and 4-bromoestranes to fluorinated benzofuranoestranes." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a028.

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Kudelko, Agnieszka, and Monika Olesiejuk. "Efficient Synthesis of Conjugated 1,2,4-Triazole Derivatives under Suzuki Cross-Coupling Reactions in the Presence of Ionic Liquids." In Chemical technology and engineering. Lviv Polytechnic National University, 2019. http://dx.doi.org/10.23939/cte2019.01.262.

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Hocek, Michal, Martina Havelková, Dalimil Dvořák, Antonín Holý, and Ivan Votruba. "Synthesis of 6-phenylpurine bases and nucleosides by Suzuki–Miyaura cross-coupling reactions of 6-chloropurines with substituted phenylboronic acids." In XIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199902027.

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