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Relevant bibliographies by topics / Suzuki Coupling

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Academic literature on the topic 'Suzuki Coupling'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 March 2023

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Journal articles on the topic "Suzuki Coupling"

1

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.

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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 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

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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.

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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 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

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Neufeldt, Sharon R., and John E. A. Russell. "C–O-Selective Cross-Coupling of Chlorinated Phenol Derivatives." Synlett 32, no. 15 (May 8, 2021): 1484–91. http://dx.doi.org/10.1055/a-1503-6330.

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AbstractChemoselective cross-coupling of phenol derivatives is valuable for generating products that retain halides. Here we discuss recent developments in selective cross-couplings of chloroaryl phenol derivatives, with a particular focus on reactions of chloroaryl tosylates. The first example of a C–O-selective Ni-catalyzed Suzuki–Miyaura coupling of chloroaryl tosylates is discussed in detail.1 Introduction2 Density Functional Theory Studies on Oxidative Addition at Nickel(0)3 Stoichiometric Oxidative Addition Studies4 Development of a Tosylate-Selective Suzuki Coupling5 Conclusion and Outlook

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Barde, E., A. Guérinot, and J. Cossy. "α-Arylation of Amides from α-Halo Amides Using Metal-Catalyzed Cross-Coupling Reactions." Synthesis 51, no. 01 (December 7, 2018): 178–84. http://dx.doi.org/10.1055/s-0037-1611358.

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Metal-catalyzed α-arylation of amides from α-halo amides with organometallic reagents is reviewed. The article includes Suzuki–Miyaura, Kumada–Corriu, Negishi, and Hiyama cross-coupling reactions.1 Introduction2 Suzuki–Miyaura Cross-Coupling2.1 Palladium Catalysis2.2 Nickel Catalysis3 Kumada–Corriu Cross-Coupling3.1 Nickel Catalysis3.2 Iron Catalysis3.3 Cobalt Catalysis4 Negishi Cross-Coupling5 Hiyama Cross-Coupling6 Conclusion

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SUZUKI, Akira. "Organoborane coupling reactions (Suzuki coupling)." Proceedings of the Japan Academy, Series B 80, no. 8 (2004): 359–71. http://dx.doi.org/10.2183/pjab.80.359.

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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 in a green environment for Suzuki reaction (Suzuki-Miyaura cross-coupling reaction). This review epitomizes the Suzuki-Miyaura cross-coupling reaction using efficient catalysts in various green media.

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Buchspies, Jonathan, and Michal Szostak. "Recent Advances in Acyl Suzuki Cross-Coupling." Catalysts 9, no. 1 (January 8, 2019): 53. http://dx.doi.org/10.3390/catal9010053.

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Acyl Suzuki cross-coupling involves the coupling of an organoboron reagent with an acyl electrophile (acyl halide, anhydride, ester, amide). This review provides a timely overview of the very important advances that have recently taken place in the acylative Suzuki cross-coupling. Particular emphasis is directed toward the type of acyl electrophiles, catalyst systems and new cross-coupling partners. This review will be of value to synthetic chemists involved in this rapidly developing field of Suzuki cross-coupling as well as those interested in using acylative Suzuki cross-coupling for the synthesis of ketones as a catalytic alternative to stoichiometric nucleophilic additions or Friedel-Crafts reactions.

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Ferrer Flegeau, Emmanuel, Matthew E. Popkin, and Michael F. Greaney. "Suzuki Coupling of Oxazoles." Organic Letters 8, no. 12 (June 2006): 2495–98. http://dx.doi.org/10.1021/ol060591j.

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Steven, Alan. "Micelle-Mediated Chemistry in Water for the Synthesis of Drug Candidates." Synthesis 51, no. 13 (May 21, 2019): 2632–47. http://dx.doi.org/10.1055/s-0037-1610714.

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Micellar reaction conditions, in a predominantly aqueous medium, have been developed for transformations commonly used by synthetic chemists working in the pharmaceutical industry to discover and develop drug candidates. The reactions covered in this review are the Suzuki–Miyaura, Miyaura borylation, Sonogashira coupling, transition-metal-catalysed CAr–N coupling, SNAr, amidation, and nitro reduction. Pharmaceutically relevant examples of these applications will be used to show how micellar conditions can offer advantages in yield, operational ease, amount of waste generated, transition-metal catalyst loading, and safety over the use of organic solvents, irrespective of the setting in which they are used.1 Introduction2 Micelles as Solubilising Agents3 Micelles as Nanoreactors4 Designer Surfactants5 A Critical Evaluation of the Case for Chemistry in Micelles6 Scope of Review7 Suzuki–Miyaura Coupling8 Miyaura Borylation9 Sonogashira Coupling10 Transition-Metal-Catalysed CAr–N Couplings11 SNAr12 Amidation13 Nitro Reduction14 Micellar Sequences15 Summary and Outlook

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Çakır, Sinem, Serdar Batıkan Kavukcu, Hande Karabıyık, Senthil Rethinam, and Hayati Türkmen. "C(acyl)–C(sp²) and C(sp²)–C(sp²) Suzuki–Miyaura cross-coupling reactions using nitrile-functionalized NHC palladium complexes." RSC Advances 11, no. 60 (2021): 37684–99. http://dx.doi.org/10.1039/d1ra07231e.

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Nitrile-functionalized Pd(ii) complexes have evaluated for the Suzuki–Miyaura cross-coupling reactions. The highest TON value was reached for the acylative Suzuki–Miyaura cross-coupling reaction of acyl chlorides with phenylboronic acids.

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Dissertations / Theses on the topic "Suzuki Coupling"

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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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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 transmetalation or prior hydrolysis to the boronic acid under SM conditions remains unknown. This research aimed to elucidate the mechanism of this cross-coupling process. Initial results under typical SM conditions created a biphasic reaction, promoted by the inorganic base and solvent composition, and showed that the boronic esters and corresponding boronic acid couple at the same absolute rate. This is thought to be a consequence of the formation of a biphasic mixture, rendering phase transfer the turnover-limiting step. The conditions were thus adapted to maintain a monophasic system using an organic soluble base, 2-tert-butyl-1,1,3,3-tetramethylguanidine, enabling the focus to be transmetalation as the turnover-limiting step. These new conditions show a significant difference in both reaction rate and induction period when using a boronic ester compared to the corresponding boronic acid. The use of guanidine was also shown to have an interesting effect on the boronic acid/ester species by 19F and 11B NMR. Further studies found the use of guanidine to create a boronate species, with this species being an aryl trihydroxyboronate or the hydroxyl"ate"-complex of the boronic ester, depending on the presence of diol in the system. Formation of a boronate species was found to be crucial for efficient cross-coupling. When testing weaker bases, unable to form a boronate species, poor SM cross-coupling conversion was found using the newly developed phosphine-free guanidine conditions, showing the importance of the boronate species under these conditions. The results suggest that depending on the strength of base used, the pathway of transmetalation pathway can be switched, between the boronate pathway and the oxo-palladium pathway, under the specific conditions developed.

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Fyfe, James William Buchanan. "Chemoselective Suzuki-Miyaura cross-coupling enabled by speciation control." Thesis, University of Strathclyde, 2017. http://digitool.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=27909.

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Boronic acids and esters are one of the most widely used compound classes inorganic chemistry. Recently, diboron systems have emerged as a powerful approach towards complex molecule synthesis. Selectivity in these systems is typically achieved through the use of protecting group strategies in which one boron residue is rendered unreactive under the prevailing reaction conditions, allowing selective manipulation of an unprotected unit. However, while these methods offer excellent selectivity, they do have the drawback of requiring additional synthetic manipulations, i.e., removal of the protecting group to allow subsequent functionalisation, limiting the overall efficiency of these processes. Boronic acids and esters undergo complex equilibria in solution. We have shown that control of these equilibria has been leveraged during the Suzuki-Miyaura reaction to enable the formation of a new, reactive BP in ester without the need for additional protecting group manipulations. Extensive optimisation identified that the nature of the base and quantity of water in the reaction were key in controlling the speciation events in the reaction. This allowed the generation of a broad substrate scope of formally homologated BPin esters. These newly generated reactive boron species were then reacted in situ in an iterative process, forming either terminal triaryl or contolled homologation products. The reaction was also found to have a temperature dependence, where under identical controlled basic conditions either the homologated BPin or the cross-coupled BMIDA species could be obtained based purely upon the temperature of the reaction. A series of control reactions aided in identifying the key processes in the reaction and, more importantly, the order in which these processes must occur in order to achieve the desired reaction. This work led to the development of methods to enable chemoselective reactions within non-protected diboron systems. This demonstrated how chemoselective Suzuki-Miyaura cross-coupling can be achieved within boronic acid/BPin esterdiboron systems by exploiting kinetic control of transmetallation while maintaining control of solution speciation events. This allows the selective reaction of boronic acids in the presence of BPin esters again without the need for protecting group manipulations, as either additional synthetic steps or in situ. Chemoselective transmetallation was then combined with chemoselective oxidative addition in order to establish the first complete chemoselective control over two of the three key mechanistic processes of the Suzuki-Miyaura reaction. This enables a one-pot sequential chemoselective Suzuki-Miyaura reaction without the requirement for any in situ modification of the reaction conditions (temperature change, sequential addition) or reactants (protecting group removal, boron species interconversion).

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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 reaction is achievable even though the desired amount of product was not obtained. However, the high yield in ni-DES can be obtained by choosing 4-bromobenzotrifluoride or 4-bromoanisole as the aryl bromide with arylboronic acid that possess the electron donating groups. Despite that, for getting more yield through Suzuki reaction in ni-DES more studies on optimization are required.

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Elmalem, Einat. "Synthesis of π-conjugated polymers via Suzuki cross-coupling polymerization." Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608242.

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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 specific surface areas and high density of surface organoboron reactive sites by various functional groups. Prior to modification by Suzuki coupling, the surface of silica gel was functionalized by phenylboronic acid. Two methods were tested for immobilization of phenylboronic acid: hydrosilylation and thiol-ene coupling. The later radical reaction between surface alkylthiol groups and 4-vinylphenylboronic acid was found more effective. Obtained boronated silica gel was used for further functionalization by various aryl halides. Surface Suzuki coupling reaction was catalyzed by palladium acetate in the presence of cesium carbonate as a base, while dimethylformamide was chosen as a solvent. The coupling reactions proceeded at mild heating under constant sonication. Such ultrasonic irradiation was reported earlier to have an activating effect on Suzuki coupling. The analysis of the obtained products indicated formation of surface biaryl compounds, the highest yields have been obtained in reactions with iodobenzene and bromobenzene. Thus, novel functionalized organic/inorganic hybrid materials were successfully synthesized by surface modification of mesoporous silica gel.

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Andert, William D. "Palladium Catalyzed Suzuki-Miyaura Cross-Coupling of Axially Chiral Biaryls." The Ohio State University, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=osu1367536419.

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Smith, Paul James. "Palladium catalysed Suzuki cross-coupling reactions in ambient temperature ionic liquids." Thesis, Imperial College London, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.405785.

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Baltus, Christine B. "Suzuki-Miyaura mediated biphenyl synthesis : a spotlight on the boronate coupling partner." Thesis, University of Greenwich, 2011. http://gala.gre.ac.uk/8038/.

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The biaryl motif is found in many natural and synthetic products that display a wide range of biological activities. This explains why biphenyls are widely encountered in medicinal chemistry as a privileged scaffold. The palladium-catalysed Suzuki-Miyaura (SM) coupling is one of the most important and efficient strategies for the synthesis of symmetrical and unsymmetrical biaryl compounds; the arylboronic acid or ester is a key partner in this coupling reaction. This work presents the synthesis of a library of new molecules containing the biphenyl scaffold; o-, m- and p-(bromomethyl)phenylboronic acid pinacol esters, 2a-c, were selected as coupling partners. Nucleophilic substitution of the bromide was carried out with amine, thiol, alcohol or phenol nucleophiles. Supported reagents and microwave assisted organic synthesis conditions were employed to enhance this chemistry and made it amenable to parallel synthesis. The resulting arylboronates were used in SM coupling reactions in order to obtain a range of biphenyls. The use of Boc-piperazine as a nucleophile in the SN2 reaction, with 2a-c, and 1-bromo-, 2-, 3- or 4-nitrobenzene or 2-bromo-5-nitropyridine as aryl halides in the SM coupling reaction, allowed two other points of functionalisation to be added to the biaryl motif. The conditions for the SM coupling of mercaptomethylphenylboronic esters and orthosubstituted methylphenylboronic esters were optimised in order to broaden the scope of the biaryl library. Phosphines were found to be good nucleophiles in the SN2 reaction with 2a-c. A Wittig reaction was performed with the resulting phosphonium arylboronates in order to synthesise arylboronic esters containing an alkene function prior the reduction of the resulting double bond of the stilbene derivatives and realising a SM coupling to synthesise arylethylbiphenyls. The stilbene derivatives were also synthesised by using the olefin cross-metathesis reaction of 4-vinylphenylboronic acid pinacol ester. A solid state crystallographic study was undertaken on a small library of methylbiphenylamides to compare the crystal structures of isomers or biphenyls with different functional groups.

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Books on the topic "Suzuki Coupling"

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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"

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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.

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Li, Jie Jack. "Suzuki coupling." In Name Reactions, 367. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_282.

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Abreu, Ana S., Paula M. T. Ferreira, Maria-João R. P. Queiroz, Jie Wu, Lisha Wang, Reza Fathi, Zhen Yang, et al. "Suzuki Coupling Reactions." In Catalysts for Fine Chemical Synthesis, Volume 3, Metal Catalysed Carbon-Carbon Bond-Forming Reactions, 59–90. Chichester, UK: John Wiley & Sons, Ltd, 2005. http://dx.doi.org/10.1002/0470862017.ch4.

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Li, Jie Jack. "Suzuki–Miyaura coupling." In Name Reactions, 593–94. Cham: 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, 536–37. Berlin, Heidelberg: 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, 530–32. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_147.

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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, 51–88. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118609811.ch3.

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Ding, Yun. "On-DNA Suzuki-Miyaura Cross-Coupling." In Methods in Molecular Biology, 45–48. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2545-3_7.

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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, 113–33. Cham: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01490-6_6.

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Nguyen, Remi, Virinder S. Parmar, and Christophe Len. "Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling in Continuous Flows." In Greener Synthesis of Organic Compounds, Drugs and Natural Products, 119–35. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003089162-7.

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Conference papers on the topic "Suzuki Coupling"

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Vieira, Lucas Campos Curcino, and Arlene G. Corrêa. "Green synthesis of chalcone derivatives via Suzuki coupling." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0238-1.

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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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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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Li, Jia-Zhe, and Xue-Feng Bai. "Ultrasonic Synthesis of Pd/SBA-15 Catalyst for Suzuki-Miyaura Coupling." In 2017 7th International Conference on Advanced Design and Manufacturing Engineering (ICADME 2017). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/icadme-17.2017.86.

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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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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. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01227.

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Gomes, S. L. S., A. M. Costa, G. C. G. Militão, P. R. R. Costa, and A. J. M. da Silva. "Synthesis of Lapachol Analogues through Suzuki-Miyaura Cross-Coupling. Antitumoral Evaluation." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0034-1.

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Lopes, Raquel de Oliveira, Benedikt Reichart, Toma Glasnov, C. Oliver Kappe, Wolfgang Kroutil, Leandro Soter de M. e. Miranda, Ivana Correa R. Leal, and Rodrigo O. M. A. de Souza. "Asymmetric enzymatic reduction and Suzuki-Miyaura coupling for the synthesis of odanacatib." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201391717510.

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Lee, Tae-Kyung, Bikash Manandhar, and Jung-Mo Ahn. "Exploration of the Scope of Suzuki–Miyaura Cross-Coupling in Peptide Ligation." In The Twenty-Third American and the Sixth International Peptide Symposium. Prompt Scientific Publishing, 2013. http://dx.doi.org/10.17952/23aps.2013.234.

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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. Basel, Switzerland: MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00173.

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