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Suzukiova reakce (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Suzukiova reakce" in Czech language version.

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44doi.org
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25nih.gov
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3hokudai.ac.jp
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1thieme.com
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1nature.com
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1worldcat.org
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  • Norio Miyaura; Kinji Yamada; Akira Suzuki. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides. Tetrahedron Letters. 1979, s. 3437–3440. Dostupné online. DOI 10.1016/S0040-4039(01)95429-2.  Archivováno 21. 10. 2014 na Wayback Machine.
  • Norio Miyaura; Akira Suzuki. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst. Chemical Communications. 1979, s. 866–867. DOI 10.1039/C39790000866. 
  • Norio Miyaura; Akira Suzuki. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds. Chemical Reviews. 1979, s. 2457–2483. Dostupné online. DOI 10.1021/cr00039a007.  Archivováno 12. 9. 2016 na Wayback Machine.
  • Akira Suzuki. Synthetic Studies via the cross-coupling reaction of organoboron derivatives with organic halides. Pure and Applied Chemistry. 1991, s. 419–422. DOI 10.1351/pac199163030419. 
  • Akira Suzuki. Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998. Journal of Organometallic Chemistry. 1999, s. 147–168. Dostupné online. DOI 10.1021/cr00039a007.  Archivováno 12. 9. 2016 na Wayback Machine.
  • K. Matos; J. A. Soderquist. Alkylboranes in the Suzuki−Miyaura Coupling: Stereochemical and Mechanistic Studies. The Journal of Organic Chemistry. 1998, s. 461–470. DOI 10.1021/jo971681s. PMID 11672034. 
  • Christian Amatore; Anny Jutand; Gaëtan Le Duc. Kinetic Data for the Transmetalation/Reductive Elimination in Palladium-Catalyzed Suzuki-Miyaura Reactions: Unexpected Triple Role of Hydroxide Ions Used as Base. Chemistry: A European Journal. 2011-02-18, s. 2492–2503. DOI 10.1002/chem.201001911. PMID 21319240. 
  • George B. Smith; George C. Dezeny; David L. Hughes; Anthony O. King; Thomas R. Verhoeven. Mechanistic Studies of the Suzuki Cross-Coupling Reaction. The Journal of Organic Chemistry. 1994-12-01, s. 8151–8156. DOI 10.1021/jo00105a036. 
  • Karl Matos; John A. Soderquist. Alkylboranes in the Suzuki−Miyaura Coupling: Stereochemical and Mechanistic Studies. The Journal of Organic Chemistry. 1998-02-01, s. 461–470. DOI 10.1021/jo971681s. PMID 11672034. 
  • John K. Stille; Kreisler S. Y. Lau. Mechanisms of oxidative addition of organic halides to Group 8 transition-metal complexes. Accounts of Chemical Research. 1977, s. 434–442. DOI 10.1021/ar50120a002. 
  • Arturo L. Casado; Pablo Espinet. On the Configuration Resulting from Oxidative Addition of RX to Pd(PPh3)4and the Mechanism of the cis-to-trans Isomerization of \PdRX(PPh3)2] Complexes (R = aryl, X = halide)†. Organometallics. 1998, s. 954–959. DOI 10.1021/om9709502. 
  • Advanced Organic Chemistry. [s.l.]: Springer, 2007. Dostupné online. DOI 10.1002/tcr.201300001. PMID 23568378. S. 739–747. 
  • Brian H. Ridgway; K. A. Woerpel. Transmetalation of Alkylboranes to Palladium in the Suzuki Coupling Reaction Proceeds with Retention of Stereochemistry. The Journal of Organic Chemistry. 1998, s. 458–460. DOI 10.1021/jo970803d. PMID 11672033. 
  • Matthew N. Hopkinson; Christian Richter; Michael Schedler; Frank Glorius. An overview of N-heterocyclic carbenes. Nature. 2014, s. 485–496. Dostupné online. ISSN 1476-4687. DOI 10.1038/nature13384. PMID 11672033. 
  • Albert L. Casalnuovo; Calabrese. Palladium-catalyzed alkylations in aqueous media. Journal of the American Chemical Society. 1990, s. 4324–4330. DOI 10.1021/ja00167a032. 
  • Jan H. Kirchhoff; Matthew R. Netherton; Ivory D. Hills; Gregory C. Fu. Boronic Acids: New Coupling Partners in Room-Temperature Suzuki Reactions of Alkyl Bromides. Crystallographic Characterization of an Oxidative-Addition Adduct Generated under Remarkably Mild Conditions. Journal of the American Chemical Society. 2002, s. 13662–13663. DOI 10.1021/ja0283899. PMID 12431081. 
  • Atsushi Ohtaka. Recyclable Polymer-Supported Nanometal Catalysts in Water. The Chemical Record. 2013, s. 274–285. DOI 10.1002/tcr.201300001. PMID 23568378. 
  • R. Martin; S. L. Buchwald. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands. Accounts of Chemical Research. 2008, s. 1461–1473. DOI 10.1021/ar800036s. PMID 18620434. 
  • JACKS1, Thomas E.; BELMONT, Daniel T.; BRIGGS, Christopher A.; HORNE, Nicole M.; KANTER, Gerald D.; KARRICK, Greg L.; KRIKKE, James J. Development of a Scalable Process for CI-1034, an Endothelin Antagonist. Organic Process Research & Development. 1 March 2004, s. 201–212. DOI 10.1021/op034104g. 
  • Zupeng Chen, Evgeniya Vorobyeva, Sharon Mitchell, Edvin Fako, Manuel A. Ortuño, Núria López, Sean M. Collins, Paul A. Midgley, Sylvia Richard, Gianvito Vilé, Javier Pérez-Ramírez. A heterogeneous single-atom palladium catalyst surpassing homogeneous systems for Suzuki coupling. Nature Nanotechnology. 2018, s. 702–707. Dostupné online. DOI 10.1038/s41565-018-0167-2. PMID 29941887. 
  • Aaron Balog; Dongfang Meng; Ted Kamenecka; Peter Bertinato; Dai-Shi Su; Erik J. Sorensen; Samuel J. Danishefsky. Total Synthesis of(–)-Epothilone A. Angewandte Chemie International Edition in English. 1996, s. 2801–2803. DOI 10.1002/anie.199628011. 
  • Junjia Liu; Stephen D. Lotesta; Erik J. Sorensen. A concise synthesis of the molecular framework of pleuromutilin. Chemical Communications. 2011, s. 1500–1502. DOI 10.1039/C0CC04077K. PMID 21079876. 
  • J. R. Vyvyan; Emily A. Peterson; Mari L. Stephan. An expedient total synthesis of (+/−)-caparratriene. Tetrahedron Letters. 1999, s. 4947–4949. DOI 10.1016/S0040-4039(99)00865-5. PMID 21079876. 
  • Fu-She Han. Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts. Chemical Society Reviews. 2013-01-01, s. 5270–5298. DOI 10.1039/c3cs35521g. PMID 23460083. 
  • Virgil Percec; Jin-Young Bae; Dale Hill. Aryl Mesylates in Metal Catalyzed Homocoupling and Cross-Coupling Reactions. 2. Suzuki-Type Nickel-Catalyzed Cross-Coupling of Aryl Arenesulfonates and Aryl Mesylates with Arylboronic Acids. Journal of Organic Chemistry. 1995, s. 1060–1065. DOI 10.1021/jo00109a044. 
  • Kaoru Inada; Norio Miyaura. Synthesis of Biaryls via Cross-Coupling Reaction of Arylboronic Acids with Aryl Chlorides Catalyzed by NiCl2/Triphenylphosphine Complexes. Tetrahedron. 2000, s. 8657–8660. DOI 10.1016/S0040-4020(00)00814-0. 
  • Yu-Long Zhao; You Li; Shui-Ming Li; Yi-Guo Zhou; Feng-Yi Sun; Lian-Xun Gao; Fu-She Han. A Highly Practical and Reliable Nickel Catalyst for Suzuki-Miyaura Coupling of Aryl Halides. Advanced Synthesis & Catalysis. 2011-06-01, s. 1543–1550. DOI 10.1002/adsc.201100101. 
  • Lei Wu; Jie Ling; Zong-Quan Wu. A Highly Active and Recyclable Catalyst: Phosphine Dendrimer-Stabilized Nickel Nanoparticles for the Suzuki Coupling Reaction. Advanced Synthesis & Catalysis. 2011-06-01, s. 1452–1456. DOI 10.1002/adsc.201100134. 
  • C. T. Yang; Zhen-Qi Zhang; Yu-Chen Liu; Lei Liu. Copper-Catalyzed Cross-Coupling Reaction of Organoboron Compounds with Primary Alkyl Halides and Pseudohalides. Angewandte Chemie International Edition. 2011, s. 3904–3907. DOI 10.1002/anie.201008007. PMID 21455914. 
  • R. B. Bredford; Mark A. Hall; George R. Hodges; Michael Huwe; Mark C. Wilkinson. Simple mixed Fe–Zn catalysts for the Suzuki couplings of tetraarylborates with benzyl halides and 2-halopyridines. Chemical Communications. 2009, s. 6430–6432. DOI 10.1039/B915945B. PMID 19841799. 
  • M. Nakamura; Toru Hashimoto; Kalum K. A. D. S. Kathriarachchi; Takeshi Zenmyo; Hirofumi Seike; Masaharu Nakamura. Iron-Catalyzed Alkyl-Alkyl Suzuki-Miyaura Coupling. Angewandte Chemie International Edition. 2012, s. 8834–8883. DOI 10.1002/anie.201202797. PMID 22848024. 
  • Y. Na; Soyoung Park; Soo Bong Han; Hoon Han; Sangwon Ko; Sukbok Chang. Ruthenium-Catalyzed Heck-Type Olefination and Suzuki Coupling Reactions: Studies on the Nature of Catalytic Species. Journal of the American Chemical Society. 2004, s. 250–258. DOI 10.1021/ja038742q. PMID 14709090. 
  • Nicholas A. Weires; Emma L. Baker; Neil K. Garg. Nickel-catalysed Suzuki–Miyaura coupling of amides. Nature Chemistry. 2015, s. 75–79. DOI 10.1038/nchem.2388. PMID 26673267. 
  • Gary A. Molander; Betina Biolatto. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions of Potassium Aryl- and Heteroaryltrifluoroborates. Journal of Organic Chemistry. 2003, s. 4302–4314. DOI 10.1021/jo0342368. PMID 12762730. 
  • Debra Dolliver, Bijay T. Bhattarai, Arjun Pandey, Megan L. Lanier, Amber S. Bordelon, Sarju Adhikari, Jordan A. Dinser, Patrick F. Flowers, Veronica S. Wills, Caroline L. Schneider, Kevin H. Shaughnessy, Jane N. Moore, Steven M. Raders, Timothy S. Snowden, Artie S. McKim, Frank R. Fronczek. Stereospecific Suzuki, Sonogashira, and Negishi Coupling Reactions of N-Alkoxyimidoyl Iodides and Bromides. Journal of Organic Chemistry. 2013, s. 3676–3687. DOI 10.1021/jo400179u. PMID 23534335. 
  • Andrey Asachenko; Kristina Sorochkina; Pavel Dzhevakov; Maxim Topchiy; Mikhail Nechaev. Suzuki–Miyaura Cross-Coupling under Solvent-Free Conditions. Advanced Synthesis & Catalysis. 2013, s. 3553–3557. DOI 10.1002/adsc.201300741. 
  • Changduo Pan; Zhang Liu; Huayue Wu; Jinchang Din; Jiang Cheng. Palladium catalyzed ligand-free Suzuki cross-coupling reaction. Catalysis Communications. 2008, s. 321–323. DOI 10.1016/j.catcom.2007.06.022. 
  • Adam F. Littke. Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions. Journal of the American Chemical Society. 2000, s. 4020–4028. DOI 10.1021/ja0002058. 
  • Ming-Gang Hu; Song Wei; Ai-Ai Jian. Highly Efficient Pd/C-Catalyzed Suzuki Coupling Reaction of p-(un)Substituted Phenyl Halide with (p-Substituted phenyl) Boronic Acid. Chinese Journal of Chemistry. 2007, s. 1183–1186. DOI 10.1002/cjoc.200790220. 
  • B. Saito. Alkyl−Alkyl Suzuki Cross-Couplings of Unactivated Secondary Alkyl Halides at Room Temperature. Journal of the American Chemical Society. 2007, s. 9602–9603. DOI 10.1021/ja074008l. PMID 17628067. 
  • J. V. Kingston; John G. Verkade. Synthesis and Characterization of R2PNP(iBuNCH2CH2)3N: A New Bulky Electron-Rich Phosphine for Efficient Pd-Assisted Suzuki−Miyaura Cross-Coupling Reactions. Journal of Organic Chemistry. 2007, s. 2816–2822. DOI 10.1021/jo062452l. PMID 17378611. 
  • C. Baillie; Lixin Zhang; Jianliang Xiao. Ferrocenyl Monophosphine Ligands: Synthesis and Applications in the Suzuki−Miyaura Coupling of Aryl Chlorides. Journal of Organic Chemistry. 2004, s. 7779–7782. DOI 10.1021/jo048963u. PMID 15498017. 
  • J. Han; Y. Liu; R. Guo. Facile synthesis of highly stable gold nanoparticles and their unexpected excellent catalytic activity for Suzuki-Miyaura cross-coupling reaction in water. Journal of the American Chemical Society. 2009, s. 2060–2061. DOI 10.1021/ja808935n. PMID 19170490. 
  • B. H. Lipshutz; Tue B. Petersen; Alexander R. Abela. Room-Temperature Suzuki−Miyaura Couplings in Water Facilitated by Nonionic Amphiphiles. Organic Letters. 2008, s. 1333–1336. DOI 10.1021/ol702714y. PMID 18335944. 

hokudai.ac.jp

eprints.lib.hokudai.ac.jp

nature.com

nih.gov

ncbi.nlm.nih.gov

  • K. Matos; J. A. Soderquist. Alkylboranes in the Suzuki−Miyaura Coupling: Stereochemical and Mechanistic Studies. The Journal of Organic Chemistry. 1998, s. 461–470. DOI 10.1021/jo971681s. PMID 11672034. 
  • Christian Amatore; Anny Jutand; Gaëtan Le Duc. Kinetic Data for the Transmetalation/Reductive Elimination in Palladium-Catalyzed Suzuki-Miyaura Reactions: Unexpected Triple Role of Hydroxide Ions Used as Base. Chemistry: A European Journal. 2011-02-18, s. 2492–2503. DOI 10.1002/chem.201001911. PMID 21319240. 
  • Karl Matos; John A. Soderquist. Alkylboranes in the Suzuki−Miyaura Coupling: Stereochemical and Mechanistic Studies. The Journal of Organic Chemistry. 1998-02-01, s. 461–470. DOI 10.1021/jo971681s. PMID 11672034. 
  • Advanced Organic Chemistry. [s.l.]: Springer, 2007. Dostupné online. DOI 10.1002/tcr.201300001. PMID 23568378. S. 739–747. 
  • Brian H. Ridgway; K. A. Woerpel. Transmetalation of Alkylboranes to Palladium in the Suzuki Coupling Reaction Proceeds with Retention of Stereochemistry. The Journal of Organic Chemistry. 1998, s. 458–460. DOI 10.1021/jo970803d. PMID 11672033. 
  • Matthew N. Hopkinson; Christian Richter; Michael Schedler; Frank Glorius. An overview of N-heterocyclic carbenes. Nature. 2014, s. 485–496. Dostupné online. ISSN 1476-4687. DOI 10.1038/nature13384. PMID 11672033. 
  • Jan H. Kirchhoff; Matthew R. Netherton; Ivory D. Hills; Gregory C. Fu. Boronic Acids: New Coupling Partners in Room-Temperature Suzuki Reactions of Alkyl Bromides. Crystallographic Characterization of an Oxidative-Addition Adduct Generated under Remarkably Mild Conditions. Journal of the American Chemical Society. 2002, s. 13662–13663. DOI 10.1021/ja0283899. PMID 12431081. 
  • Atsushi Ohtaka. Recyclable Polymer-Supported Nanometal Catalysts in Water. The Chemical Record. 2013, s. 274–285. DOI 10.1002/tcr.201300001. PMID 23568378. 
  • R. Martin; S. L. Buchwald. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands. Accounts of Chemical Research. 2008, s. 1461–1473. DOI 10.1021/ar800036s. PMID 18620434. 
  • Zupeng Chen, Evgeniya Vorobyeva, Sharon Mitchell, Edvin Fako, Manuel A. Ortuño, Núria López, Sean M. Collins, Paul A. Midgley, Sylvia Richard, Gianvito Vilé, Javier Pérez-Ramírez. A heterogeneous single-atom palladium catalyst surpassing homogeneous systems for Suzuki coupling. Nature Nanotechnology. 2018, s. 702–707. Dostupné online. DOI 10.1038/s41565-018-0167-2. PMID 29941887. 
  • Junjia Liu; Stephen D. Lotesta; Erik J. Sorensen. A concise synthesis of the molecular framework of pleuromutilin. Chemical Communications. 2011, s. 1500–1502. DOI 10.1039/C0CC04077K. PMID 21079876. 
  • J. R. Vyvyan; Emily A. Peterson; Mari L. Stephan. An expedient total synthesis of (+/−)-caparratriene. Tetrahedron Letters. 1999, s. 4947–4949. DOI 10.1016/S0040-4039(99)00865-5. PMID 21079876. 
  • Fu-She Han. Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts. Chemical Society Reviews. 2013-01-01, s. 5270–5298. DOI 10.1039/c3cs35521g. PMID 23460083. 
  • C. T. Yang; Zhen-Qi Zhang; Yu-Chen Liu; Lei Liu. Copper-Catalyzed Cross-Coupling Reaction of Organoboron Compounds with Primary Alkyl Halides and Pseudohalides. Angewandte Chemie International Edition. 2011, s. 3904–3907. DOI 10.1002/anie.201008007. PMID 21455914. 
  • R. B. Bredford; Mark A. Hall; George R. Hodges; Michael Huwe; Mark C. Wilkinson. Simple mixed Fe–Zn catalysts for the Suzuki couplings of tetraarylborates with benzyl halides and 2-halopyridines. Chemical Communications. 2009, s. 6430–6432. DOI 10.1039/B915945B. PMID 19841799. 
  • M. Nakamura; Toru Hashimoto; Kalum K. A. D. S. Kathriarachchi; Takeshi Zenmyo; Hirofumi Seike; Masaharu Nakamura. Iron-Catalyzed Alkyl-Alkyl Suzuki-Miyaura Coupling. Angewandte Chemie International Edition. 2012, s. 8834–8883. DOI 10.1002/anie.201202797. PMID 22848024. 
  • Y. Na; Soyoung Park; Soo Bong Han; Hoon Han; Sangwon Ko; Sukbok Chang. Ruthenium-Catalyzed Heck-Type Olefination and Suzuki Coupling Reactions: Studies on the Nature of Catalytic Species. Journal of the American Chemical Society. 2004, s. 250–258. DOI 10.1021/ja038742q. PMID 14709090. 
  • Nicholas A. Weires; Emma L. Baker; Neil K. Garg. Nickel-catalysed Suzuki–Miyaura coupling of amides. Nature Chemistry. 2015, s. 75–79. DOI 10.1038/nchem.2388. PMID 26673267. 
  • Gary A. Molander; Betina Biolatto. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions of Potassium Aryl- and Heteroaryltrifluoroborates. Journal of Organic Chemistry. 2003, s. 4302–4314. DOI 10.1021/jo0342368. PMID 12762730. 
  • Debra Dolliver, Bijay T. Bhattarai, Arjun Pandey, Megan L. Lanier, Amber S. Bordelon, Sarju Adhikari, Jordan A. Dinser, Patrick F. Flowers, Veronica S. Wills, Caroline L. Schneider, Kevin H. Shaughnessy, Jane N. Moore, Steven M. Raders, Timothy S. Snowden, Artie S. McKim, Frank R. Fronczek. Stereospecific Suzuki, Sonogashira, and Negishi Coupling Reactions of N-Alkoxyimidoyl Iodides and Bromides. Journal of Organic Chemistry. 2013, s. 3676–3687. DOI 10.1021/jo400179u. PMID 23534335. 
  • B. Saito. Alkyl−Alkyl Suzuki Cross-Couplings of Unactivated Secondary Alkyl Halides at Room Temperature. Journal of the American Chemical Society. 2007, s. 9602–9603. DOI 10.1021/ja074008l. PMID 17628067. 
  • J. V. Kingston; John G. Verkade. Synthesis and Characterization of R2PNP(iBuNCH2CH2)3N: A New Bulky Electron-Rich Phosphine for Efficient Pd-Assisted Suzuki−Miyaura Cross-Coupling Reactions. Journal of Organic Chemistry. 2007, s. 2816–2822. DOI 10.1021/jo062452l. PMID 17378611. 
  • C. Baillie; Lixin Zhang; Jianliang Xiao. Ferrocenyl Monophosphine Ligands: Synthesis and Applications in the Suzuki−Miyaura Coupling of Aryl Chlorides. Journal of Organic Chemistry. 2004, s. 7779–7782. DOI 10.1021/jo048963u. PMID 15498017. 
  • J. Han; Y. Liu; R. Guo. Facile synthesis of highly stable gold nanoparticles and their unexpected excellent catalytic activity for Suzuki-Miyaura cross-coupling reaction in water. Journal of the American Chemical Society. 2009, s. 2060–2061. DOI 10.1021/ja808935n. PMID 19170490. 
  • B. H. Lipshutz; Tue B. Petersen; Alexander R. Abela. Room-Temperature Suzuki−Miyaura Couplings in Water Facilitated by Nonionic Amphiphiles. Organic Letters. 2008, s. 1333–1336. DOI 10.1021/ol702714y. PMID 18335944. 

nobelprize.org

  • The Nobel Prize in Chemistry 2010 [online]. [cit. 2013-10-25]. Dostupné online. 

thieme.com

science-of-synthesis.thieme.com

  • Science of Synthesis: Best methods. Best results – Thieme Chemistry [online]. [cit. 2021-04-14]. Dostupné online. 

web.archive.org

whiterose.ac.uk

eprints.whiterose.ac.uk

worldcat.org