Littérature scientifique sur le sujet « Mizoroki-Heck »
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Articles de revues sur le sujet "Mizoroki-Heck":
Srivastava, Vivek. « Synthesis and Characterization of Pd exchanged MMT Clay for Mizoroki-Heck Reaction ». Open Chemistry 16, no 1 (20 juin 2018) : 605–13. http://dx.doi.org/10.1515/chem-2018-0065.
Schmidt, Bernd. « The Mizoroki-Heck Reaction ». Synthesis 2010, no 04 (février 2010) : 718. http://dx.doi.org/10.1055/s-0029-1218660.
Watson, Allan, Kirsty Wilson, Jane Murray, Helen Sneddon et Craig Jamieson. « Dimethylisosorbide (DMI) as a Bio-Derived Solvent for Pd-Catalyzed Cross-Coupling Reactions ». Synlett 29, no 17 (28 septembre 2018) : 2293–97. http://dx.doi.org/10.1055/s-0037-1611054.
Ojha, Subhadra, et Niranjan Panda. « Pd-Catalyzed desulfitative arylation of olefins by N-methoxysulfonamide ». Organic & ; Biomolecular Chemistry 20, no 6 (2022) : 1292–98. http://dx.doi.org/10.1039/d1ob02360h.
Yamazaki, Yasuomi, Tatsuki Morimoto et Osamu Ishitani. « Synthesis of novel photofunctional multinuclear complexes using a coupling reaction ». Dalton Transactions 44, no 25 (2015) : 11626–35. http://dx.doi.org/10.1039/c5dt01717c.
Kaur, Navneet, Gurpreet Kaur, Aman Bhalla, Jaspreet S. Dhau et Ganga Ram Chaudhary. « Metallosurfactant based Pd–Ni alloy nanoparticles as a proficient catalyst in the Mizoroki Heck coupling reaction ». Green Chemistry 20, no 7 (2018) : 1506–14. http://dx.doi.org/10.1039/c7gc03877a.
Shibasaki, M., T. Ohshima et W. Itano. « ChemInform Abstract : Mizoroki-Heck Reaction ». ChemInform 42, no 42 (27 septembre 2011) : no. http://dx.doi.org/10.1002/chin.201142250.
Wang, Shi-Meng, Hai-Xia Song, Xiao-Yan Wang, Nan Liu, Hua-Li Qin et Cheng-Pan Zhang. « Palladium-catalyzed Mizoroki–Heck-type reactions of [Ph2SRfn][OTf] with alkenes at room temperature ». Chemical Communications 52, no 80 (2016) : 11893–96. http://dx.doi.org/10.1039/c6cc06089g.
Shao, Linjun, et Chenze Qi. « Chitosan microspheres-supported palladium species as an efficient and recyclable catalyst for Mizoroki–Heck reaction ». New Journal of Chemistry 41, no 16 (2017) : 8156–65. http://dx.doi.org/10.1039/c7nj01918a.
Zhang, Qing-Song, Shi-Li Wan, Di Chen, Chang-Hua Ding et Xue-Long Hou. « Palladium-catalyzed asymmetric intermolecular Mizoroki–Heck reaction for construction of a chiral quaternary carbon center ». Chemical Communications 51, no 61 (2015) : 12235–38. http://dx.doi.org/10.1039/c5cc03601a.
Thèses sur le sujet "Mizoroki-Heck":
Zhou, Yuan. « Synthetic studies towards homotyrosinol sulfonamide derivatives via Heck-Mizoroki coupling reactions ». Thesis, University of British Columbia, 2009. http://hdl.handle.net/2429/16838.
Poulin, Carl. « Heck-Mizoroki reaction using palladium and nickel on yttria stabilized zirconia ». Thesis, University of Ottawa (Canada), 2008. http://hdl.handle.net/10393/28018.
Açıkel, Müge Artok Levent. « Silica Supported N-Heterocyclic Carbenes:Active and Reusable Heterogeneous Catalysts for Mizoroki-Heck Reactions/ ». [s.l.] : [s.n.], 2004. http://library.iyte.edu.tr/tezler/master/kimya/T000496.pdf.
Mabit, Thibaud. « Vers la première synthèse totale de la kidamycine : développement d’une stratégie de synthèse convergente et innovante, et mise au point d’une réaction d’aryl-C-glycosylation stéréospécifique ». Thesis, Le Mans, 2018. http://www.theses.fr/2018LEMA1023/document.
Kidamycin, former member of pluramycin family isolated from Streptomyces pluricolorescens, remains a challenging synthetic target for organic chemists since its discover in 1956. The last bastion slowing down the syntheses of this latter family is the regio- and stereoselective introduction as well as the functionnalization of both aryl-C-glycosidic subunits.We propose to develop herein a regio- and stereospecific aryl-C-glycosylation reaction via Mizoroki-Heck cross coupling enshrined in a novel and convergent strategy for the first total synthesis of kidamycin
Lopes, David. « Approches synthétiques du motif octahydro-furo[3,2-B]pyridine et d'analogues spiraniques par catalyse au palladium ». Paris 6, 2007. http://www.theses.fr/2007PA066706.
Staubitz, Anne. « Towards the asymmetric synthesis of (-)-rocaglamide and Optimisation of the Mizoroki-Heck reaction using design of experiment ». Thesis, University of Bristol, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.440140.
Tasker, Sarah Z. (Sarah Zinnen). « The nickel-catalyzed Mizoroki-Heck reaction : high regioselectivity in Olefin migratory insertion and photoredox-enabled indoline formation ». Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/101456.
This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Cataloged from student-submitted PDF version of thesis. Vita
Includes bibliographical references.
[chemical formula and color illustrations ...] Achieving high selectivity in the Heck reaction of electronically unbiased alkenes has been a longstanding challenge. Using a nickel-catalyzed cationic Heck reaction, we were able to achieve excellent selectivity for branched products (>/=19:1 in all cases) over a wide range of aryl electrophiles and aliphatic olefins. A bidentate ligand with a suitable bite angle and steric profile was key to obtaining high branched/linear selectivity, while the appropriate base suppressed alkene isomerization of the product. Though aryl triflates are traditionally used to access the cationic Heck pathway, we have shown that by using triethylsilyl trifluoromethanesulfonate we can effect a counterion exchange of the catalytic nickel complex such that cheaper and more stable aryl chlorides, mesylates, tosylates, and sulfamates can be used to yield the same branched products with high selectivity. [chemical formula and color illustrations ...] Nickel/photoredox catalysis is used to synthesize indolines in one step from iodoacetanilides and alkenes. Very high regioselectivity for 3-substituted indoline products is obtained for both aliphatic and styrenyl olefins. Mechanistic investigations indicate that oxidation to Ni(III) is necessary to perform the difficult C-N bond-forming reductive elimination, producing a Ni(I) complex which in turn is reduced to Ni(0). This process serves to further demonstrate the utility of photoredox catalysts as controlled single electron transfer agents in multi-oxidation state nickel catalysis.
by Sarah Z. Tasker.
Ph. D. in Organic Chemistry
Vogel, Sophie. « Synthèse de polycycles diazotes par réactions de cyclisation palladocatalysées ». Paris 6, 2008. http://www.theses.fr/2008PA066380.
Kirsten, Martin. « Organokatalyse : Theoretische Untersuchungen zur Claisen-Umlagerung und zum Einfluss von Azolen auf die Morita-Baylis-Hillman-Reaktion sowie neuartige Bis(carben)metallkomplexe auf der Basis von Triazolen ». Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2011. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-71134.
Fiebig, Lukas [Verfasser], Mathias [Akademischer Betreuer] Schäfer, Hans-Günther [Akademischer Betreuer] Schmalz et Christoph [Akademischer Betreuer] Schalley. « Mechanistische Studien zur Mizoroki-Heck- und zur Kobalt(I)-katalysierten Diels-Alder-Reaktion mithilfe massenspektrometrischer Methoden / Lukas Fiebig. Gutachter : Mathias Schäfer ; Hans-Günther Schmalz ; Christoph Schalley ». Köln : Universitäts- und Stadtbibliothek Köln, 2014. http://d-nb.info/107165134X/34.
Livres sur le sujet "Mizoroki-Heck":
Oestreich, Martin. The Mizoroki-Heck reaction. Hoboken, N.J : Wiley, 2008.
Oestreich, Martin, dir. The Mizoroki–Heck Reaction. Chichester, UK : John Wiley & Sons, Ltd, 2009. http://dx.doi.org/10.1002/9780470716076.
Oestreich, Martin. Mizoroki-Heck Reaction. Wiley & Sons, Incorporated, John, 2009.
Catalyzed Mizoroki–Heck Reaction or C–H activation. MDPI, 2020. http://dx.doi.org/10.3390/books978-3-03928-139-8.
Chapitres de livres sur le sujet "Mizoroki-Heck":
Oestreich, Martin. « Directed Mizoroki–Heck Reactions ». Dans Topics in Organometallic Chemistry, 169–92. Berlin, Heidelberg : Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/3418_2007_063.
Geoghegan, Kimberly. « Regioselectivity in the Heck (Mizoroki-Heck) Reaction ». Dans Selectivity in the Synthesis of Cyclic Sulfonamides, 17–41. Cham : Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-10338-9_2.
Gautam, Prashant, et Vivek Srivastava. « MMT Intercalated Pd Nanocatalyst for Heck (Mizoroki-Heck) Reaction ». Dans Nanostructured Smart Materials, 109–29. First edition. : Apple Academic Press, 2021. http://dx.doi.org/10.1201/9781003130468-7.
Barriault, Louis, et Effiette L. O. Sauer. « Asymmetric Cross-coupling and Mizoroki-Heck Reactions ». Dans Quaternary Stereocenters, 185–205. Weinheim, FRG : Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527606858.ch7.
Yamazaki, Yasuomi. « Synthesis of Multinuclear Complexes Using the Mizoroki–Heck Reaction ». Dans Development of Synthetic Methods for Novel Photofunctional Multinuclear Complexes, 7–32. Singapore : Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-7148-7_2.
Yamazaki, Yasuomi. « Selective Synthesis of Various Photofunctional Multinuclear Complexes Using a Combination of the Mizoroki–Heck Reaction and the Homo-coupling Reaction ». Dans Development of Synthetic Methods for Novel Photofunctional Multinuclear Complexes, 33–57. Singapore : Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-7148-7_3.
« Mizoroki–Heck Reaction ». Dans Stereoselective Synthesis 3, sous la direction de Evans. Stuttgart : Georg Thieme Verlag, 2011. http://dx.doi.org/10.1055/sos-sd-203-00304.
Alonso, D. A., et C. Nájera. « Mizoroki–Heck Reaction ». Dans Water in Organic Synthesis, 1. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-206-00381.
Murahashi, S. I. « The Heck–Mizoroki Reaction ». Dans Three Carbon-Heteroatom Bonds : Nitriles, Isocyanides, and Derivatives, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-019-00257.
Alonso, D. A., et C. Nájera. « The Mizoroki–Heck Reaction ». Dans Monocyclic Arenes, Quasiarenes, and Annulenes, 1. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-045-00175.
Actes de conférences sur le sujet "Mizoroki-Heck":
Lete, Esther, Ane Azcargorta, Iratxe Barbolla, Estíbaliz Coya et Nuria Sotomayor. « Asymmetric Mizoroki-Heck reactions : generation of quaternary stereocenters and cascade cyclizations ». Dans MOL2NET, International Conference on Multidisciplinary Sciences. Basel, Switzerland : MDPI, 2015. http://dx.doi.org/10.3390/mol2net-1-a007.
Sotomayor, Nuria, Ane Azcargorta et Esther Lete. « Diastereoselective formation of tertiary stereocenters via Mizoroki-Heck reaction ». Dans MOL2NET, International Conference on Multidisciplinary Sciences. Basel, Switzerland : MDPI, 2015. http://dx.doi.org/10.3390/mol2net-1-a008.
Lete, Esther, Estibaliz Coya et Nuria Sotomayor. « Intramolecular enantioselective Mizoroki-Heck reactions of 2-alkenyl (o-halobenzyl)pyrroles ». Dans MOL2NET 2016, International Conference on Multidisciplinary Sciences, 2nd edition. Basel, Switzerland : MDPI, 2016. http://dx.doi.org/10.3390/mol2net-02-08013.
Movassagh, Barahman, et Shahriar Yasham. « Cryptand-22 as an Efficient Ligand for the Palladium-Catalyzed Mizoroki-Heck Reaction under Air ». Dans The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland : MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a010.
Shao, Linjun, Yijun Du et Chenze Qi. « Pd nanoparticles entrapped in chitosan superfine fibers as a highly active and stable catalyst for the Mizoroki–Heck reaction ». Dans 3rd China-Japan Joint Workshop on Positron Science (JWPS2017). Japan Society of Applied Physics, 2018. http://dx.doi.org/10.7567/jjapcp.7.011201.