Relevant bibliographies by topics / Palladium catalyzed cross-coupling

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Academic literature on the topic 'Palladium catalyzed cross-coupling'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 February 2022

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Journal articles on the topic "Palladium catalyzed cross-coupling"

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Yang, Yang. "Palladium-Catalyzed Cross-Coupling of Nitroarenes." Angewandte Chemie International Edition 56, no. 50 (2017): 15802–4. http://dx.doi.org/10.1002/anie.201708940.

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Stradiotto, M., and R. Lundgren. "Palladium-Catalyzed Cross-Coupling with Hydrazine." Synfacts 2011, no. 02 (2011): 0204. http://dx.doi.org/10.1055/s-0030-1259236.

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Sain, Shalu, Sonika Jain, Manish Srivastava, Rajendra Vishwakarma, and Jaya Dwivedi. "Application of Palladium-Catalyzed Cross-Coupling Reactions in Organic Synthesis." Current Organic Synthesis 16, no. 8 (2020): 1105–42. http://dx.doi.org/10.2174/1570179416666191104093533.

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: Palladium-catalyzed cross-coupling reactions have gained a continuously growing interest of synthetic organic chemists. The present review gives a brief account of applications of the palladium-catalyzed cross-coupling reactions in comprehensive synthesis, viz., the Heck, Stille, Suzuki–Miyaura, Negishi, Sonogashira, Buchwald–Hartwig, Ullmann and the Oxidative, decarboxylative cross-coupling reactions, with particular emphasis on the synthesis of heterocyclic compounds.
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Yuasa, Akihiro, Kazunori Nagao та Hirohisa Ohmiya. "Allylic cross-coupling using aromatic aldehydes as α-alkoxyalkyl anions". Beilstein Journal of Organic Chemistry 16 (7 лютого 2020): 185–89. http://dx.doi.org/10.3762/bjoc.16.21.

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The allylic cross-coupling using aromatic aldehydes as α-alkoxyalkyl anions is described. The synergistic palladium/copper-catalyzed reaction of aromatic aldehydes, allylic carbonates, and a silylboronate produces the corresponding homoallylic alcohol derivatives. This process involves the catalytic formation of a nucleophilic α-silyloxybenzylcopper(I) species and the subsequent palladium-catalyzed allylic substitution.
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Zhang, Zhen, Zongyang Li, Bin Fu, and Zhenhua Zhang. "Palladium-catalyzed cross-coupling reaction of azides with isocyanides." Chemical Communications 51, no. 91 (2015): 16312–15. http://dx.doi.org/10.1039/c5cc05981j.

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Gagnon, A., M. Duplessis, P. Alsabeh, and F. Barabé. "Palladium-Catalyzed Cross-Coupling Reactions with Tricyclopropylbismuth." Synfacts 2008, no. 7 (2008): 0744. http://dx.doi.org/10.1055/s-2008-1077832.

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Orellana, Arturo, David Rosa, Andrei Nikolaev, and Nisha Nithiy. "Palladium-Catalyzed Cross-Coupling Reactions of Cyclopropanols." Synlett 26, no. 04 (2015): 441–48. http://dx.doi.org/10.1055/s-0034-1380156.

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Becica, Joseph, Oliver R. J. Heath, Cameron H. M. Zheng, and David C. Leitch. "Palladium‐Catalyzed Cross‐Coupling of Alkenyl Carboxylates." Angewandte Chemie 132, no. 39 (2020): 17430–34. http://dx.doi.org/10.1002/ange.202006586.

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Becica, Joseph, Oliver R. J. Heath, Cameron H. M. Zheng, and David C. Leitch. "Palladium‐Catalyzed Cross‐Coupling of Alkenyl Carboxylates." Angewandte Chemie International Edition 59, no. 39 (2020): 17277–81. http://dx.doi.org/10.1002/anie.202006586.

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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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Dissertations / Theses on the topic "Palladium catalyzed cross-coupling"

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Ruiz-Castillo, Paula. "Palladium-catalyzed C-N and C-O cross-coupling reactions." Thesis, Massachusetts Institute of Technology, 2016. http://hdl.handle.net/1721.1/105048.

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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 (pages 375-410).<br>Chapter 1: This chapter describes a general method for the of the Pd-catalyzed N-arylation of hindered [alpha],[alpha],[alpha]-trisubstituted primary amines. The reaction utilized catalysts based on two biaryl phosphine ligands, which were developed via kinetics-based mechanistic analysis and rational design. These studies led to the first example of catalyst based on a hybrid (alkyl)aryl b
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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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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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García, Melchor Maximiliano. "Theoretical Study on Pd-catalyzed Cross-Coupling Reactions." Doctoral thesis, Universitat Autònoma de Barcelona, 2012. http://hdl.handle.net/10803/96827.

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D’ençà el seu descobriment, fa ja prop de tres dècades, les reaccions d’acoblament creuat C-C catalitzades per Pd han esdevingut una de les transformacions més poderoses dins la química organometàl·lica. De fet, tres dels desenvolupadors de les reaccions d’acoblament més emprades (reaccions de Heck, Suzuki i Negishi) van ésser guardonats l'any 2010 amb el premi Nobel de Química. El mecanisme general de les reaccions d'acoblament creuat C-C consisteix en tres etapes: addició oxidant, transmetal·lació, i eliminació reductiva. La millora d’una reacció comporta el coneixement profund del seu mecan
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Batten, Amanda Lynn. "Accessing Chemically Differentiated 1,5-dienes Through Palladium Catalyzed Allyl-Allyl Cross-Coupling with Internal Allyl Electrophiles." Thesis, Boston College, 2015. http://hdl.handle.net/2345/bc-ir:104708.

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Thesis advisor: James P. Morken<br>Internal allyl electrophiles were successfully implemented in a catalytic cross-coupling to allylB(pin) with high regiocontrol to afford multisubstituted 1,5-dienes bearing chemically differentiated olefins. Construction of alkenyl compounds with all carbon quaternary centers and high enantiomeric excess can be achieved in one step without the use of enantiomerically enriched chiral ligands<br>Thesis (MS) — Boston College, 2015<br>Submitted to: Boston College. Graduate School of Arts and Sciences<br>Discipline: Chemistry
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Kamikawa, Takashi. "Enantioselectivity and Chemoselectivity in Palladium-Catalyzed Grignard Cross-Coupling of Aryl Triflates." 京都大学 (Kyoto University), 1998. http://hdl.handle.net/2433/157165.

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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・論文博士<br>博士(理学)<br>乙第9788号<br>論理博第1334号<br>新制||理||1061(附属図書館)<br>UT51-98-G387<br>(主査)教授 林 民生, 教授 鈴木 仁美, 教授 大須賀 篤弘<br>学位規則第4条第2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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Dennis, Joseph Michael Jr. "Palladium- and nickel-catalyzed C-N cross-coupling reactions featuring soluble organic bases." Thesis, Massachusetts Institute of Technology, 2020. https://hdl.handle.net/1721.1/128408.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 2020<br>Cataloged from the PDF of thesis. "The Table of Contents does not accurately represent the page numbering"--Disclaimer page.<br>Includes bibliographical references.<br>Chapter 1: Breaking the Base Barrier: An Electron-Deficient Palladium Catalyst Enables the Use of a Common Soluble Base in C-N Coupling Due to the low intrinsic acidity of amines, palladium-catalyzed C-N cross-coupling plagued continuously by the necessity to employ strong, inorganic, or insoluble bases. To surmount the many Due to the low in
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McAvoy, Camille Z. "Palladium-catalyzed C-N cross-coupling reactions toward the synthesis of drug-like molecules." Thesis, Massachusetts Institute of Technology, 2012. http://hdl.handle.net/1721.1/73388.

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Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Chemistry; and, (S.B.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 2012.<br>Cataloged from PDF version of thesis.<br>Includes bibliographical references (p. ).<br>The development of methodologies for C-N bond formation reactions is an important scientific challenge because of many academic and industrial applications. This work will focus particularly on palladium-catalyzed cross-couplings of amine-containing compounds with aryl halides. The scope of the BrettPhos precatalyst for the cross-coupling of ort
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Le, Hai. "Developments in palladium catalyzed reactions: Strategies to synthesize asymmetric 1,5-dienes and 1,4-dicarbonyls." Thesis, Boston College, 2014. http://hdl.handle.net/2345/bc-ir:104389.

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Thesis advisor: James P. Morken<br>This dissertation details recent developments in palladium catalyzed carbon-carbon bond formation reactions with two areas of focus: the palladium catalyzed branched and enantioselective allyl-allyl cross-coupling, and the palladium catalyzed carbonylative conjugate addition. Allyl-allyl cross-coupling presents an opportunity to synthesize 1,5-dienes, a scaffold that resembles subunits of terpenes, a critical building block in nature. Chapter I provides an overview of the developments in the allyl-allyl cross-coupling area. Chapter II, III, and IV detail stra
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Books on the topic "Palladium catalyzed cross-coupling"

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

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Fang, Yuanqing. Palladium-catalysed Heck reaction and tandem cross coupling reactions for heterocycle synthesis. 2007.

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Book chapters on the topic "Palladium catalyzed cross-coupling"

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Shaughnessy, Kevin H. "Cross-Coupling Reactions in Aqueous Media." In Palladium-Catalyzed Coupling Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648283.ch7.

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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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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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Tsuji, Jiro, and Tadakatsu Mandai. "Palladium-Catalyzed Coupling Reactions of Propargylic Compounds." In Metal-Catalyzed Cross-Coupling Reactions. Wiley-VCH Verlag GmbH, 2007. http://dx.doi.org/10.1002/9783527612222.ch11.

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Bäckvall, Jan-E. "Palladium-Catalyzed 1,4-Additions to Conjugated Dienes." In Metal-Catalyzed Cross-Coupling Reactions. Wiley-VCH Verlag GmbH, 2007. http://dx.doi.org/10.1002/9783527612222.ch8.

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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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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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Negishi, Ei-Ichi, and Fang Liu. "Palladium- or Nickel-Catalyzed Cross-Coupling with Organometals Containing Zinc, Magnesium, Aluminum, and Zirconium." In Metal-Catalyzed Cross-Coupling Reactions. Wiley-VCH Verlag GmbH, 2007. http://dx.doi.org/10.1002/9783527612222.ch1.

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Bäckvall, Jan-Erling. "Palladium-Catalyzed 1,4-Additions to Conjugated Dienes." In Metal-Catalyzed Cross-Coupling Reactions and More. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527655588.ch11.

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Paradies, Jan. "Palladium-Catalyzed Aromatic Carbon-Nitrogen Bond Formation." In Metal-Catalyzed Cross-Coupling Reactions and More. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527655588.ch13.

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Conference papers on the topic "Palladium catalyzed cross-coupling"

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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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Lavén, Gaston, and Jacek Stawinski. "Synthetic studies on the preparation of dinucleoside phenylphosphonates and phenylphosphonothioates via palladium(0) catalysed cross-coupling." In XIIIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2005. http://dx.doi.org/10.1135/css200507195.

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You might also be interested in the extended bibliographies on the topic 'Palladium catalyzed cross-coupling' for particular source types:
Journal articles Dissertations / Theses
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