Relevant bibliographies by topics / Palladium catalyzed reaction

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

Academic literature on the topic 'Palladium catalyzed reaction'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Palladium catalyzed reaction"

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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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Christodoulou, Michael S., Egle M. Beccalli, and Sabrina Giofrè. "Palladium-Catalyzed Benzodiazepines Synthesis." Catalysts 10, no. 6 (2020): 634. http://dx.doi.org/10.3390/catal10060634.

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This review is focused on palladium-catalyzed reactions as efficient strategies aimed at the synthesis of different classes of benzodiazepines. Several reaction typologies are reported including hydroamination, amination, C–H arylation, N-arylation, and the Buchwald–Hartwig reaction, depending on the different substrates identified as halogenated starting materials (activated substrates) or unactivated unsaturated systems, which then exploit Pd(0)- or Pd(II)-catalytic species. In particular, the use of the domino reactions, as intra- or intermolecular processes, are reported as an efficient an
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Mukai, Shoma, and Nathan Werner. "Synthesis and Palladium-Catalyzed Cross-Coupling of an Alkyl-Substituted Alkenylboronic Acid Pinacol Ester with Aryl Bromides." American Journal of Undergraduate Research 20, no. 1 (2023): 37–46. http://dx.doi.org/10.33697/ajur.2023.078.

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The palladium-catalyzed cross-coupling reaction of alkyl-substituted alkenylboron reagents with aryl halides is a versatile method to introduce a hydrophobic hydrocarbon chain onto organic compounds of interest. The application of the cross-coupling reaction is enabled by synthetic methods for the preparation of alkenylboron reagents. The geometrically pure, alkyl-substituted alkenylboron reagent, (E)-octenylboronic acid pinacol ester, was prepared by 9-BBN-catalyzed hydroboration reaction of 1-octene with pinacolborane in refluxing 1 M THF solution. This reagent was then evaluated in palladiu
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Yang, Jia, Tieqiao Chen, Yongbo Zhou, Shuangfeng Yin, and Li-Biao Han. "Palladium-catalyzed dehydrogenative coupling of terminal alkynes with secondary phosphine oxides." Chemical Communications 51, no. 17 (2015): 3549–51. http://dx.doi.org/10.1039/c4cc09567g.

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The palladium-catalyzed dehydrogenative coupling of alkynes with secondary phosphine oxides is developed. Thus, in the presence of a silver additive, palladium acetate could efficiently catalyze the dehydrocoupling of secondary phosphine oxides with a variety of alkynes to produce the corresponding alkynylphosphine oxides in high yields. A reaction mechanism is proposed.
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Peng, Jin-Bao, Xin-Lian Liu, Lin Li, and Xiao-Feng Wu. "Palladium-catalyzed enantioselective carbonylation reactions." Science China Chemistry 65, no. 3 (2022): 441–61. http://dx.doi.org/10.1007/s11426-021-1165-6.

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AbstractCarbonylation, one of the most powerful approaches to the preparation of carbonylated compounds, has received significant attention from researchers active in various fields. Indeed, impressive progress has been made on this subject over the past few decades. Among the various types of carbonylation reactions, asymmetric carbonylation is a straightforward methodology for constructing chiral compounds. Although rhodium-catalyzed enantioselective hydroformylations have been discussed in several elegant reviews, a general review on palladium-catalyzed asymmetric carbonylations is still mi
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P., G. More, V. Dalave N., S. Lawand A., and M. Nalawade A. "Palladium catalyzed cross-coupling reactions of organomercurials." Journal of Indian Chemical Society Vol. 86, Jan 2009 (2009): 68–71. https://doi.org/10.5281/zenodo.5807134.

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Department of Chemistry, Solapur University, Solapur-413 255, Maharashtra, India <em>Fax</em> : 91-217-2744770 Ramkrishna Paramhansa College, Osmanabad-413 501, Maharashtra, India <em>Manuscript received 31 January 2008, accepted 9 September 2008</em> The palladium catalyzed cross-coupling reactions of methyl mercury iodide provide a mild, selective and general method for the construction of new C-C bond i.e. for the synthesis of arenes. The reaction proceeds in DMF, in the presence of a nucleophilic catalyst (iodide ion), at room temperature under argon atmosphere. Pd<sup>0</sup> which is gen
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Rifhat Bibi, Rifhat Bibi, Muhammad Yaseen Muhammad Yaseen, Haseen Ahmad Haseen Ahmad, Ismat Ullah Khan Ismat Ullah Khan, Shaista Parveen Shaista Parveen, and Abbas Hassan Abbas Hassan. "Palladium Catalyzed Synthesis of Phenylquinoxaline-Alkyne Derivatives via Sonogashira Cross Coupling Reaction." Journal of the chemical society of pakistan 43, no. 1 (2021): 95. http://dx.doi.org/10.52568/000550.

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Transition metals mediated cross coupling methodologies provide an extremely powerful versatile pathway in organic syntheses undoubtedly, a facile route for syntheses and derivatization of biologically important heterocycles from easily available precursors. Sonogashira coupling reaction, a leading method to Csp-Csp2 bond formation is one of the most important and rapid pathways to couple aryl/vinyl halides with terminal alkynes. Current research study deals with the synthesis of alkyne substituted quinoxaline derivatives. The quinoxalines class of aromatic heterocycles exhibits a wide variety
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Rifhat Bibi, Rifhat Bibi, Muhammad Yaseen Muhammad Yaseen, Haseen Ahmad Haseen Ahmad, Ismat Ullah Khan Ismat Ullah Khan, Shaista Parveen Shaista Parveen, and Abbas Hassan Abbas Hassan. "Palladium Catalyzed Synthesis of Phenylquinoxaline-Alkyne Derivatives via Sonogashira Cross Coupling Reaction." Journal of the chemical society of pakistan 43, no. 1 (2021): 95. http://dx.doi.org/10.52568/000550/jcsp/43.01.2021.

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Transition metals mediated cross coupling methodologies provide an extremely powerful versatile pathway in organic syntheses undoubtedly, a facile route for syntheses and derivatization of biologically important heterocycles from easily available precursors. Sonogashira coupling reaction, a leading method to Csp-Csp2 bond formation is one of the most important and rapid pathways to couple aryl/vinyl halides with terminal alkynes. Current research study deals with the synthesis of alkyne substituted quinoxaline derivatives. The quinoxalines class of aromatic heterocycles exhibits a wide variety
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Rifhat Bibi, Rifhat Bibi, Muhammad Yaseen Muhammad Yaseen, Haseen Ahmad Haseen Ahmad, Ismat Ullah Khan Ismat Ullah Khan, Shaista Parveen Shaista Parveen, and Abbas Hassan Abbas Hassan. "Palladium Catalyzed Synthesis of Phenylquinoxaline-Alkyne Derivatives via Sonogashira Cross Coupling Reaction." Journal of the chemical society of pakistan 43, no. 1 (2021): 95. http://dx.doi.org/10.52568/000009.

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Transition metals mediated cross coupling methodologies provide an extremely powerful versatile pathway in organic syntheses undoubtedly, a facile route for syntheses and derivatization of biologically important heterocycles from easily available precursors. Sonogashira coupling reaction, a leading method to Csp-Csp2 bond formation is one of the most important and rapid pathways to couple aryl/vinyl halides with terminal alkynes. Current research study deals with the synthesis of alkyne substituted quinoxaline derivatives. The quinoxalines class of aromatic heterocycles exhibits a wide variety
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Baranano, David, Grace Mann, and John F. Hartwig. "Nickel and Palladium-Catalyzed Cross-Couplings that Form Carbon-Heteroatom and Carbon-Element Bonds." Current Organic Chemistry 1, no. 3 (1997): 287–305. http://dx.doi.org/10.2174/1385272801666220124194647.

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The transition-metal catalyzed addition of heteroatom nucleophiles to aryl and vinyl halides is reviewed. This chemistry typically involves a nickel- or palladium-based catalyst containing phosphine ligands. In recently developed palladium-catalyzed chemistry, aryl halides react with amines in the presence of base to form arylamines. In similar chemistry cataly­zed by both nickel and palladium, aryl and vinyl halides react with alkali metal or tin thiolates or selenides to form aryl and vinyl sulfides, while the reaction of different phosphorus compounds, such as phosphides, phosphonates, and
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Dissertations / Theses on the topic "Palladium catalyzed reaction"

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Fujino, Daishi. "Studies on Palladium-Catalyzed Arylative Cyclization Reactions." 京都大学 (Kyoto University), 2014. http://hdl.handle.net/2433/188508.

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Cavarischia, Claudia. "Synthesis of natural organic compounds via Palladium-catalyzed reactions." Doctoral thesis, La Sapienza, 2005. http://hdl.handle.net/11573/917350.

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Arrechea, Pedro Luis. "Mechanistic studies on palladium-catalyzed C-N cross-coupling reaction." Thesis, Massachusetts Institute of Technology, 2016. http://hdl.handle.net/1721.1/107561.

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Thesis: Ph. D. in Organic Chemistry, Massachusetts Institute of Technology, Department of Chemistry, 2016.<br>Cataloged from PDF version of thesis.<br>Includes bibliographical references.<br>Mechanistic studies on the palladium catalyzed C-N bond-forming reaction were carried out to generate a more complete understanding of the catalytic cycle. To understand this reaction, several kinetic studies employing simple aryl halide and amine coupling partners were performed to elucidate unknown reaction pathways. Chapter 1. The resting state for the palladium catalyzed cross-coupling of various diary
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Yano, Takaaki. "Synthesis of Benzocyclobutenones Using Phosphonates and Phosphonation Reaction Catalyzed by Palladium." Kyoto University, 2018. http://hdl.handle.net/2433/232060.

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Akram, Sadia. "Synthesis of Dibenzofurans via a Palladium Catalyzed Oxidative Ring Closure Reaction." ScholarWorks@UNO, 2013. http://scholarworks.uno.edu/honors_theses/29.

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The cannabinoid partial agonist BAY 59-3704 has been identified as an attractive target to explore structure-activity relationships at cannabinoid receptors for the development of a therapeutic agent for psychostimulant addiction. This thesis will describe the studies associated with the optimization of a palladium-catalyzed oxidative ring closure reaction for the synthesisof dibenzofuran analogues from substituted diaryl ethers. These dibenzofurans are viewed as rigid analogues of BAY 59-3704 and will provide useful information about molecular interactions at cannabinoid receptors. The scope
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Liu, Yang. "Studies on Palladium-Catalyzed [3+2]-Annulation/Domino Reactions." Thesis, Sorbonne université, 2019. http://www.theses.fr/2019SORUS214.

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Ce travail de thèse est consacré à l'étude des réactions d'annélation [3+2] domino catalysées au palladium. Tout d'abord, une nouvelle séquence domino a été développée, qui implique la réaction entre les dérivés cycliques α,β-insaturés-γ-oxy-carbonylés et les acétamides stabilisés par résonance. Les pyrrolidine-2-ones bicycliques obtenues ont été générées par une allylation intermoléculaire catalysée au Pd, suivie d'une réaction d’aza-Michael intramoléculaire. Une version asymétrique a également été réalisée, obtenant jusqu'à 60% d’excès énantiomérique. Ensuite, une nouvelle séquence domino tr
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Tolstoy, Päivi. "Synthesis and Evaluation of N,P-Chelating Ligands in Asymmetric Transition-Metal-Catalyzed Reactions : Ir-Catalyzed Asymmetric Hydrogenation and Pd-Catalyzed Asymmetric Intermolecular Heck Reaction." Doctoral thesis, Uppsala universitet, Institutionen för biokemi och organisk kemi, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-108940.

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This thesis describes synthesis of new chiral N,P ligands and their evaluation in two types of asymmetric transition-metal catalyzed reactions. The first part of the thesis describes studies in iridium-catalyzed asymmetric hydrogenation. A new class of chiral N,P ligands, imidazole-phosphines, was synthesized and evaluated in the Ir-catalyzed asymmetric hydrogenation of olefins (Paper I). The new ligands proved to be highly efficient and enantioselective in the reaction. Because the substrate scope of Ir-catalyzed asymmetric hydrogenation is still limited to certain types of test substrates, n
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Danjo, Hiroshi. "New Amphiphilic Palladium-Phosphine Complexes Bound to Solid Supports : Preparation and Use for Palladium-Catalyzed Reaction in Aqueous Media." 京都大学 (Kyoto University), 1999. http://hdl.handle.net/2433/157178.

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本文データは平成22年度国立国会図書館の学位論文(博士)のデジタル化実施により作成された画像ファイルを基にpdf変換したものである<br>Kyoto University (京都大学)<br>0048<br>新制・課程博士<br>博士(理学)<br>甲第7681号<br>理博第2066号<br>新制||理||1095(附属図書館)<br>UT51-99-G275<br>京都大学大学院理学研究科化学専攻<br>(主査)教授 林 民生, 教授 大須賀 篤弘, 教授 鈴木 仁美<br>学位規則第4条第1項該当
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Yang, Yuan. "Graphene as a Solid-state Ligand for Palladium Catalyzed Cross-coupling Reactions." VCU Scholars Compass, 2018. https://scholarscompass.vcu.edu/etd/5488.

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Palladium-catalyzed carbon-carbon cross-coupling reactions have emerged a broadly useful, selective and widely applicable method to synthesize pharmaceutical active ingredients. As currently practiced in the pharmaceutical industry, homogeneous Pd catalysts are typically used in cross-coupling reactions. The rational development of heterogeneous catalysts for cross-coupling reactions is critical for overcoming the major drawbacks of homogeneous catalysis including difficulties in the separation, purification, and quality control process in drug production. In order to apply heterogeneous catal
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喜教, 鈴間. "Asymmetric addition reaction of organoboronic acid catalyzed by palladium with ferrocene-based phosphine ligand." Thesis, https://doors.doshisha.ac.jp/opac/opac_link/bibid/BB10352112/?lang=0, 2010. https://doors.doshisha.ac.jp/opac/opac_link/bibid/BB10352112/?lang=0.

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Books on the topic "Palladium catalyzed reaction"

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

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Seo, Tamae. Palladium-Catalyzed Mechanochemical Cross-Coupling Reactions. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-1991-4.

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Molnár, Árpád. Palladium-catalyzed coupling reactions: Practical aspects and future developments. Wiley-VCH, 2013.

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Malleron, Jean-Luc. Handbook of palladium-catalyzed organic reactions: Synthetic aspects and catalytic cycles. Academic Press, 1997.

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Malleron, Jean-Luc. Handbook of palladium-catalyzed organic reactions: Synthetic aspects and catalytic cycles. Academic, 1997.

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Harben, Spencer M. Synthesis of conjugated polyenes via palladium-catalysed cross-coupling reactions. University of East Anglia, 1991.

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fakulteten, Uppsala universitet Farmaceutiska, and Uppsala universitet, eds. Regio-controlled and fast intermolecular heck reactions: Palladium-catalyzed coupling reactions with microwave heating. Acta Universitatis Upsaliensis, 1997.

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Gerritsma, David Alexander. Phospha-adamantane ligands and phosphorous ionic liquids for palladium-catalyzed cross-coupling reactions. Brock University, Dept. of Chemistry, 2004.

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Karabelas, Kostas. Palladium-catalysed vinylic substitution reactions of vinyl- and allylsilanes: Effects of added silver ions. Chemical Center, 1988.

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Handbook of Palladium-Catalyzed Organic Reactions. Elsevier, 1997. http://dx.doi.org/10.1016/b978-0-12-466615-3.x5000-9.

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Book chapters on the topic "Palladium catalyzed reaction"

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Seo, Tamae. "Solid-State Suzuki–Miyaura Cross-Coupling Reaction Using Mechanochemistry." In Palladium-Catalyzed Mechanochemical Cross-Coupling Reactions. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-1991-4_3.

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Bräse, Stefan, and Armin De Meijere. "Palladium-Catalyzed Coupling of Organyl Halides to Alkenes - the Heck Reaction." In Metal-Catalyzed Cross-Coupling Reactions. Wiley-VCH Verlag GmbH, 2007. http://dx.doi.org/10.1002/9783527612222.ch3.

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Köhler, Klaus, Katharina Wussow, and Andreas Sebastian Wirth. "Palladium-Catalyzed Cross-Coupling Reactions - A General Introduction." In Palladium-Catalyzed Coupling Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648283.ch1.

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Huang, Lin, and Pui Kwan Wong. "Nature of the True Catalytic Species in CarbonCarbon Coupling Reactions with Heterogeneous Palladium Precatalysts." In Palladium-Catalyzed Coupling Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648283.ch10.

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Reynolds, William R., and Christopher G. Frost. "Coupling Reactions in Continuous-Flow Systems." In Palladium-Catalyzed Coupling Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648283.ch11.

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Dumrath, Andreas, Christa Lübbe, and Matthias Beller. "Palladium-Catalyzed Cross-Coupling Reactions - Industrial Applications." In Palladium-Catalyzed Coupling Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648283.ch12.

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Okumura, Kazu. "High-Turnover Heterogeneous Palladium Catalysts in Coupling Reactions: The Case of Pd Loaded on Dealuminated Y Zeolites." In Palladium-Catalyzed Coupling Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648283.ch2.

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Salih, Kifah S. M., and Werner R. Thiel. "Palladium-Catalyzed Coupling Reactions with Magnetically Separable Nanocatalysts." In Palladium-Catalyzed Coupling Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648283.ch3.

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Molnár, Árpád. "The Use of Ordered Porous Solids as Support Materials in Palladium-Catalyzed Cross-Coupling Reactions." In Palladium-Catalyzed Coupling Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648283.ch4.

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Karimi, Babak, Sedigheh Abedi, and Asghar Zamani. "Coupling Reactions Induced by Polymer-Supported Catalysts." In Palladium-Catalyzed Coupling Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648283.ch5.

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Conference papers on the topic "Palladium catalyzed reaction"

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Frota, Carlise, Allan F. C. Rossini, Rogério A. Gariani, and Cristiano Raminelli. "Selective coupling reaction between 2,6-diiodoanisoles and terminal alkynes catalyzed by palladium complex." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0057-1.

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Jr., Palimécio G. Guerrero, Paulo R. de Oliveira, Adriano C. M. Baroni, Francisco A. Marques, Gabriela R. Hurtado, and Miguel J. Dabdoub. "Total synthesis of targretin via palladium catalyzed crosscoupling reaction of a vinyl organozinc intermediate." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0324-1.

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Movassagh, Barahman, and Shahriar Yasham. "Cryptand-22 as an Efficient Ligand for the Palladium-Catalyzed Mizoroki-Heck Reaction under Air." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a010.

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De Oliveira Vigier, Karine, Christophe Coutanceau, and Steve Baranton. "Electro-oxidation of glycerol and diglycerol in the presence of Pt or Pd-based electrocatalyst follows by the reductive amination of the products obtained." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/olba8004.

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The selective electro-oxidation of bio-based organic molecules such as glycerol, polyglycerols, saccharides and furanic compounds has received particular attention in recent years, due to the high value-added compounds that result and their numerous industrial applications. Electrochemical methods are therefore well suited for the controlled oxidation of small organic molecules in aqueous media. Glycerol valorization through partial oxidation is a good way of obtaining many different molecules with high added value such as glyceric acid, tartronic acid, dihydroxyacetone, glyceraldehyde etc.,
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Joy, Muthipeedika Nibin, and Vasiliy A. Bakulev. "Is nonaflate a better leaving group than corresponding triflate? A case study in the palladium catalyzed cross-coupling reaction of 7-substituted coumarins." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087323.

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Kalek, Marcin, and Jacek Stawinski. "Synthetic studies on the P–C bond formation via a palladium-catalyzed cross-coupling reaction. Application to the synthesis of P-arylated nucleic acids." In XIVth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2008. http://dx.doi.org/10.1135/css200810214.

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Bao, Zhenan, and Luping Yu. "Exploration of palladium-catalyzed reactions for the synthesis of conjugated polymers." In SPIE's 1995 International Symposium on Optical Science, Engineering, and Instrumentation, edited by Sze C. Yang and Prasanna Chandrasekhar. SPIE, 1995. http://dx.doi.org/10.1117/12.219548.

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Ortiz de Elguea, Verónica, Nuria Sotomayor, and Esther Lete. "Intramolecular Palladium-catalyzed C-H activation reactions: Synthesis of substituted quinolones." In MOL2NET 2016, International Conference on Multidisciplinary Sciences, 2nd edition. MDPI, 2016. http://dx.doi.org/10.3390/mol2net-02-h008.

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Matos, Maria, Eugenio Uriarte, Fernanda Borges, and Saleta Vazquez-Rodriguez. "Alternative Methodologies for the Synthesis of Substituted 3-arylcoumarins: Perkin Reactions and Palladium-Catalyzed Synthesis." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00376.

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Chin-Wei Hsu, Wei-Yen Wang, Shao-Hua Wang, Yu-Hsiang Kao, and Tzu-Chien Wei. "Adhesive nickel-phosphorous electroless plating on silanized silicon wafer catalyzed by reactive palladium nanoparticles." In 2015 10th International Microsystems, Packaging, Assembly and Circuits Technology Conference (IMPACT). IEEE, 2015. http://dx.doi.org/10.1109/impact.2015.7365244.

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