Relevant bibliographies by topics / Palladium catalyzed C-C bond forming

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  2. Dissertations / Theses
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Academic literature on the topic 'Palladium catalyzed C-C bond forming'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Palladium catalyzed C-C bond forming"

1

Liu, Yang, Zhongyi Mao, Alexandre Pradal, Pei-Qiang Huang, Julie Oble, and Giovanni Poli. "Palladium-Catalyzed [3 + 2]-C–C/N–C Bond-Forming Annulation." Organic Letters 20, no. 13 (2018): 4057–61. http://dx.doi.org/10.1021/acs.orglett.8b01616.

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Korwar, Sudha, Michael Burkholder, Stanley E. Gilliland, Kendra Brinkley, B. Frank Gupton, and Keith C. Ellis. "Chelation-directed C–H activation/C–C bond forming reactions catalyzed by Pd(ii) nanoparticles supported on multiwalled carbon nanotubes." Chemical Communications 53, no. 52 (2017): 7022–25. http://dx.doi.org/10.1039/c7cc02122d.

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Punia, Lavisha, Karu Ramesh, and Gedu Satyanarayana. "Palladium mediated domino reaction: synthesis of isochromenes under aqueous medium." RSC Advances 10, no. 1 (2020): 338–49. http://dx.doi.org/10.1039/c9ra08792c.

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Pilgrim, Ben S., Alice E. Gatland, Carlos H. A. Esteves, et al. "Palladium-catalyzed enolate arylation as a key C–C bond-forming reaction for the synthesis of isoquinolines." Organic & Biomolecular Chemistry 14, no. 3 (2016): 1065–90. http://dx.doi.org/10.1039/c5ob02320c.

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Kanchana, U. S., Elizabeth J. Diana, Thomas V. Mathew, and Gopinathan Anilkumar. "Palladium‐ Catalyzed C−P Bond Forming Reactions: An Overview." ChemistrySelect 6, no. 7 (2021): 1579–88. http://dx.doi.org/10.1002/slct.202004433.

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Rathin, Jana. "Synthesis of 1-Methoxyphenanthrene by Palladium-Catalyzed Heck Reaction." International Journal of HIT Transaction on ECCN Vol. 7, no. 2A (2021) (2021): 12–17. https://doi.org/10.5281/zenodo.5893120.

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Department of Chemistry, ShahidMatanginiHazra Govt. General Degree College for Women, Nimtouri, West Bengal A novel methodology for the synthesis of 1-methoxy phenanthrene has been developed via a palladium-assisted 6π electrocyclic reaction followed by formaldehyde elimination.
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Shaikh, Azam M., Bharat K. Sharma, Sajeev Chacko, and Rajesh M. Kamble. "Synthesis and opto-electrochemical properties of tribenzo[a,c,i]phenazine derivatives for hole transport materials." RSC Advances 6, no. 96 (2016): 94218–27. http://dx.doi.org/10.1039/c6ra20964e.

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In this work, five novel 3,6-disubstituted-tribenzo[a,c,i]phenazine (2–6) derivatives were synthesized in good yield by employing a palladium catalyzed C–N bond forming amination reaction and fully characterized.
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8

Cribbin, Liam, Brendan Twamley, Nicolae Buga, et al. "C–C Coupling in sterically demanding porphyrin environments." Beilstein Journal of Organic Chemistry 20 (November 4, 2024): 2784–98. http://dx.doi.org/10.3762/bjoc.20.234.

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Unlike their planar counterparts, classic synthetic protocols for C–C bond forming reactions on nonplanar porphyrins are underdeveloped. The development of C–C bond forming reactions on nonplanar porphyrins is critical in advancing this field of study for more complex porphyrin architectures, which could be used in supramolecular assemblies, catalysis, or sensing. In this work a library of arm-extended dodecasubstituted porphyrins was synthesized through the optimization of the classic Suzuki–Miyaura coupling of peripheral haloaryl substituents with a range of boronic acids. We report on palla
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Xie, Hujun, Ting Fan, Qunfang Lei, and Wenjun Fang. "New progress in theoretical studies on palladium-catalyzed C−C bond-forming reaction mechanisms." Science China Chemistry 59, no. 11 (2016): 1432–47. http://dx.doi.org/10.1007/s11426-016-0018-2.

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Shaikh, Azam M., Bharat K. Sharma, Sajeev Chacko, and Rajesh M. Kamble. "Synthesis and optoelectronic investigations of triarylamines based on naphtho[2,3-f]quinoxaline-7,12-dione core as donor–acceptors for n-type materials." RSC Advances 6, no. 65 (2016): 60084–93. http://dx.doi.org/10.1039/c6ra11149a.

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We have synthesized a new series of fully characterized donor–acceptor systems (2–7) involving electron donor triarylamines and electron acceptor naphtho[2,3-f]quinoxaline-7,12-dione by employing palladium catalyzed C–N bond forming amination reactions in good yields.
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Dissertations / Theses on the topic "Palladium catalyzed C-C bond forming"

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Szymaniak, Adam Anthony. "Nonracemic Organoboronates by Transition Metal-Catalyzed C-C and C-Si Bond Forming Reactions." Thesis, Boston College, 2018. http://hdl.handle.net/2345/bc-ir:108119.

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Thesis advisor: James P. Morken<br>This dissertation will describe the development of three transition metal-catalyzed syntheses of nonracemic organoboronates. The first chapter explains the development of a palladium-catalyzed enantiotopic-group-selective cross-coupling of geminal bis(boronates) with alkenyl electrophiles. This process enables the synthesis of highly valuable nonracemic disubstituted allylic boronates. Chapter two describes a palladium-induced 1,2-metallate rearrangement of vinylboron “ate” complexes. The newly developed process incorporates an alternative route for the trans
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Anderson, Kevin William. "Expanding the substrate scope in palladium-catalyzed C-N and C-C bond-forming reactions." Thesis, Massachusetts Institute of Technology, 2006. http://hdl.handle.net/1721.1/36255.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2006.<br>Vita.<br>Includes bibliographical references.<br>Chapter 1. The first detailed study of the palladium-catalyzed amination of aryl nonaflates is reported. Use of bulky electron-rich monophosphinobiaryl ligands or BINAP allow for the catalytic amination of electron-rich and -neutral aryl nonaflates with both primary and secondary amines. Using XantPhos, the catalytic amination of a variety of functionalized aryl nonaflates resulted in excellent yields of anilines; even 2-carboxymethyl aryl nonaflate is effective
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Brace, Gareth Neil. "Applications of palladium-catalysed C-N bond forming reactions." Thesis, University of Bath, 2006. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.428381.

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Rousseaux, Sophie. "Palladium-Catalyzed C(sp2)-C(sp3) Bond Formation." Thèse, Université d'Ottawa / University of Ottawa, 2012. http://hdl.handle.net/10393/23058.

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Palladium-catalyzed reactions for carbon-carbon bond formation have had a significant impact on the field of organic chemistry in recent decades. Illustrative is the 2010 Nobel Prize, awarded for “palladium-catalyzed cross couplings in organic synthesis”, and the numerous applications of these transformations in industrial settings. This thesis describes recent developments in C(sp2)-C(sp3) bond formation, focusing on alkane arylation reactions and arylative dearomatization transformations. In the first part, our contributions to the development of intramolecular C(sp3)-H arylation reactions
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Huang, Xiaohua 1973. "Palladium-catalyzed C-C, C-N and C-O bond formation." Thesis, Massachusetts Institute of Technology, 2003. http://hdl.handle.net/1721.1/29639.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2003.<br>Vita.<br>Includes bibliographical references.<br>New methods for Pd-catalyzed cross-coupling reactions of aryl halides or arenesulfonates are described. Key to the success of these transformations is the proper choice of ligand and reaction conditions. Palladium catalysts supported by bulky, monodentate phosphine ligands with a biaryl backbone or the bidentate ligand, Xantphos, effectively promote the formation of ca-aryl carbonyl compounds. Base-sensitive functional groups are better tolerated when a weak bas
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Laren, Martijn Wouter van. "Palladium-catalyzed C-H and C-N bond formation." [S.l. : Amsterdam : s.n.] ; Universiteit van Amsterdam [Host], 2004. http://dare.uva.nl/document/75422.

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Wolfe, John P. (John Perry) 1970. "Late transition metal catalyzed C-N and C-C bond forming reactions." Thesis, Massachusetts Institute of Technology, 1999. http://hdl.handle.net/1721.1/9521.

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Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 1999.<br>Includes bibliographical references.<br>New methods for the palladium-catalyzed amination of aryl halides are described. Key to these is the development of new catalysts and reaction conditions for these transformations. Initially, P(o-tol)3 ligated palladium catalysts were investigated but gave way to systems that used chelating phosphine ligands which substantially expanded the scope of the catalytic amination methodology. Palladium catalyst systems based on BINAP ((2,2'-diphenylphosphino)-1, 1 '-binaphthyl)
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Yang, Yang Ph D. Massachusetts Institute of Technology. "New reactivity and selectivity in transition metal-catalyzed C-C and C-N bond forming processes." Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/101558.

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Thesis: Ph. D. in Organic Chemistry, Massachusetts Institute of Technology, Department of Chemistry, 2015.<br>Cataloged from PDF version of thesis. Volume 1 (page 1 to page 510) ; Volume 2 (page 511 to 881). Duplicated pages for pages 195 to 240 are bound after page 881.<br>Includes bibliographical references.<br>Part I. Palladium-Catalyzed Carbon-Carbon Bond Forming Cross-Couplings Chapter 1. Ligand-Controlled Palladium-Catalyzed Regiodivergent Suzuki-Miyaura Cross-Coupling of Allylboronates and Aryl Halides An orthogonal set of catalyst systems based on the use of two biarylphosphine ligands
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Aoki, Yuma. "Development of Iron-Catalyzed C-N and C-C Bond Forming Reactions toward Functional Arylamine Synthesis." Kyoto University, 2019. http://hdl.handle.net/2433/242518.

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Tang, Jie [Verfasser], and Lukas [Akademischer Betreuer] Goossen. "Palladium/Copper Bimetallic Catalyzed Decarboxylative C-C Bond Formations / Jie Tang ; Betreuer: Lukas Goossen." Kaiserslautern : Technische Universität Kaiserslautern, 2017. http://d-nb.info/1123572100/34.

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Books on the topic "Palladium catalyzed C-C bond forming"

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Kapdi, Anant R., and Debabrata Maiti. Strategies for Palladium-Catalyzed Non-Directed and Directed C Bond H Bond Functionalization. Elsevier, 2017.

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Kapdi, Anant R., and Debabrata Maiti. Strategies for Palladium-Catalyzed Non-Directed and Directed C-H Bond Functionalization. Elsevier Science & Technology Books, 2017.

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3

Leeuwen, Piet van. Enantioselective C-C Bond Forming Reactions: From Metal Complex-, Organo-, and Bio-Catalyzed Perspectives. Elsevier Science & Technology Books, 2023.

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Leeuwen, Piet van. Enantioselective C-C Bond Forming Reactions: From Metal Complex-, Organo-, and Bio-Catalyzed Perspectives. Elsevier Science & Technology, 2023.

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5

Raheem, Izzat Tiedje. I. Enantioselective total synthesis of quinine and quinidine: II. Thiourea-catalyzed enantioselective C-C bond-forming reactions : a. catalytic asymmetric N-Acyliminium ion cyclizations : b. catalytic asymmetric aza-Baylis-Hillman reactions. 2008.

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Book chapters on the topic "Palladium catalyzed C-C bond forming"

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Lemen, Georgia S., and John P. Wolfe. "Palladium-Catalyzed sp2 C–N Bond Forming Reactions: Recent Developments and Applications." In Amination and Formation of sp2 C-N Bonds. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/3418_2012_56.

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Ball, Catherine J., and Michael C. Willis. "Synthesis of Aromatic Benzo-Fused Five- and Six-Membered Heterocycles via Palladium- and Copper-Catalyzed CX Bond-Forming Reactions." In Transition-Metal-Mediated Aromatic Ring Construction. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118629871.ch24.

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Liu, Guosheng, and Yichen Wu. "Palladium-Catalyzed Allylic C–H Bond Functionalization of Olefins." In C-H Activation. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/128_2009_16.

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You, Shu-Li, and Ji-Bao Xia. "Palladium-Catalyzed Aryl–Aryl Bond Formation Through Double C–H Activation." In C-H Activation. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/128_2009_18.

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Echavarren, Antonio M., and Anna Homs. "Mechanistic Aspects of Metal-Catalyzed C,C- and C,X-Bond Forming Reactions." In Metal-Catalyzed Cross-Coupling Reactions and More. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527655588.ch1.

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Sako, Makoto, Shinobu Takizawa, and Hiroaki Sasai. "Chapter 18. Vanadium-catalyzed Enantioselective C–C Bond-forming Reactions." In Catalysis Series. Royal Society of Chemistry, 2020. http://dx.doi.org/10.1039/9781839160882-00446.

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Dana, Suman, M. Ramu Yadav, and Akhila K. Sahoo. "Ruthenium-Catalyzed C−N and C−O Bond-Forming Processes from C−H Bond Functionalization." In C-H Bond Activation and Catalytic Functionalization I. Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_126.

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Wang, Guan-Wu. "Functionalization of [60]Fullerene via Palladium-Catalyzed C–H Bond Activation." In C-H Bond Activation and Catalytic Functionalization I. Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_128.

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Wolfe, John P., Joshua D. Neukom, and Duy H. Mai. "Synthesis of Saturated Five-Membered Nitrogen Heterocycles via Pd-Catalyzed CN Bond-Forming Reactions." In Catalyzed Carbon-Heteroatom Bond Formation. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch1.

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Takizawa, Shinobu, and Hiroaki Sasai. "Metal-Catalyzed Enantio- and Diastereoselective C-C Bond-Forming Reactions in Domino Processes." In Domino Reactions. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527671304.ch11.

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Conference papers on the topic "Palladium catalyzed C-C bond forming"

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Ganapathy, D., and G. Sekar. "An efficient and reusable palladium nanocatalyst in C-C bond forming cross-coupling reactions." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201386477.

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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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