Relevant bibliographies by topics / Stille coupling reactions

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

Academic literature on the topic 'Stille coupling reactions'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Stille coupling reactions"

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Pires, Marina, Sara Purificação, A. Santos, and M. Marques. "The Role of PEG on Pd- and Cu-Catalyzed Cross-Coupling Reactions." Synthesis 49, no. 11 (2017): 2337–50. http://dx.doi.org/10.1055/s-0036-1589498.

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Carbon–carbon and carbon–heteroatom coupling reactions are among the most important transformations in organic synthesis as they enable complex structures to be formed from readily available compounds under different routes and conditions. Several metal-catalyzed cross-coupling reactions have been developed creating many efficient methods accessible for the direct formation of new bonds between differently hybridized carbon atoms.During the last decade, much effort has been devoted towards improvement of the sustainability of these reactions, such as catalyst recovery and atom efficiency. Poly
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Pattenden, Gerald, and Davey Stoker. "Stille Cross-Coupling Reactions Using Vinylcyclopropylstannanes." Synlett 2009, no. 11 (2009): 1800–1802. http://dx.doi.org/10.1055/s-0029-1217327.

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Huang, Hongyan, Guanyuan Jiao, Shuli Liu, et al. "Unprecedented side reactions in Stille coupling: desired ones for Stille polycondensation." Chemical Communications 51, no. 87 (2015): 15846–49. http://dx.doi.org/10.1039/c5cc05404d.

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Clapham, Bruce, and Andrew J. Sutherland. "Stille Coupling Reactions of 4-Substituted-2,5-Diphenyloxazoles†." Journal of Organic Chemistry 66, no. 26 (2001): 9033–37. http://dx.doi.org/10.1021/jo0107150.

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Hrizi, Asma, Manon Cailler, Moufida Romdhani-Younes, Yvan Carcenac, and Jérôme Thibonnet. "Synthesis of New Highly Functionalized 1H-Indole-2-carbonitriles via Cross-Coupling Reactions." Molecules 26, no. 17 (2021): 5287. http://dx.doi.org/10.3390/molecules26175287.

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An approach for the preparation of polysubstituted indole-2-carbonitriles through a cross-coupling reaction of compounds 1-(but-2-ynyl)-1H-indole-2-carbonitriles and 1-benzyl-3-iodo-1H-indole-2-carbonitriles is described. The reactivity of indole derivatives with iodine at position 3 was studied using cross-coupling reactions. The Sonogashira, Suzuki–Miyaura, Stille and Heck cross-couplings afforded a variety of di-, tri- and tetra-substituted indole-2-carbonitriles.
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Quayle, Peter, Jingyang Wang, Jie Xu, and Christopher J. Urch. "Stereoselective Stille coupling reactions of 1,1-bis(trialkylstannyl)ethenes." Tetrahedron Letters 39, no. 5-6 (1998): 485–88. http://dx.doi.org/10.1016/s0040-4039(97)10583-4.

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Larhed, Mats, Masahide Hoshino, Sabine Hadida, Dennis P. Curran, and Anders Hallberg. "Rapid Fluorous Stille Coupling Reactions Conducted under Microwave Irradiation." Journal of Organic Chemistry 62, no. 16 (1997): 5583–87. http://dx.doi.org/10.1021/jo970362y.

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Fürstner, Alois, Jacques-Alexis Funel, Martin Tremblay, et al. "A versatile protocol for Stille–Migita cross coupling reactions." Chemical Communications, no. 25 (2008): 2873. http://dx.doi.org/10.1039/b805299a.

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Thiele, Christina M., and Terence N. Mitchell. "Short communication: Stille coupling reactions of functionalized triorganotin halides." Applied Organometallic Chemistry 18, no. 2 (2004): 83–85. http://dx.doi.org/10.1002/aoc.585.

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Larson, Gerald. "Some Aspects of the Chemistry of Alkynylsilanes." Synthesis 50, no. 13 (2018): 2433–62. http://dx.doi.org/10.1055/s-0036-1591979.

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In amongst the considerable chemistry of acetylenes there lies some unique chemistry of alkynylsilanes (silylacetylenes) some of which is reviewed herein. This unique character is exemplified not only in the silyl protection of the terminal C–H of acetylenes, but also in the ability of the silyl group to be converted into other functionalities after reaction of the alkynylsilane and to its ability to dictate and improve the regioselectivity of reactions at the triple bond. This, when combined with the possible subsequent transformations of the silyl group, makes their chemistry highly versatil
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Dissertations / Theses on the topic "Stille coupling reactions"

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Chamoin, Sylvie. "Aryl-aryl Stille and Suzuzi-Miyaura cross-coupling reactions on solid support." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0022/NQ51184.pdf.

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Muscroft-Taylor, Andrew Clive. "Investigations of the type ii intramolecular Diels-Alder reaction directed toward natural product synthesis." Thesis, University of Canterbury. Chemistry, 2006. http://hdl.handle.net/10092/1290.

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This thesis describes synthetic studies directed towards the total synthesis of the nakafuran and florlide marine natural products. Chapter One provides an overview of the importance of natural products to current medicinal chemistry and describes how the "supply issue" associated with these biologically derived compounds can be resolved through the process of total synthesis. Two families of marine natural products, the nakafurans and the florlides, are introduced as synthetic targets and strategies utilising a type II intramolecular Diels-Alder (IMDA) reaction to achieve their total synthesi
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Nguyen, Thi Minh Ngoc. "Stille Coupling Reactions Involving α-Alkoxybenzylstannanes". Thesis, 2007. http://hdl.handle.net/10012/3453.

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The Stille reaction has established itself as one of the two most general and most selective palladium-catalyzed cross-coupling reactions, along with the Suzuki cross-coupling of organoboron compounds. The Stille coupling of α-alkoxystannanes is a relatively unexplored area. A previous study showed that an α-alkoxyalkylstannane could be coupled with benzoyl chloride with retention of configuration. However, our group has recently shown that Stille couplings of sulfonamidobenzylstannanes proceeds with inversion of configuration. In order to determine whether the Stille coupling reaction of
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Chang, Fen-Ping, and 張芬萍. "Recyclable Palladium Bipyridyl Complexes Catalyzed Stille Coupling Reaction." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/v6g84w.

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碩士<br>國立臺北科技大學<br>有機高分子研究所<br>95<br>ABSTRACT Title：Recyclable Palladium Bipyridyl Complexes Catalyzed Stlle Coupling Reaction School：National Taipei University of Technology Pages：108 Department：Institute of Organic and Polymeric Materials Time：July, 2007 Degree：Master Researcher：Fen-Ping Chang Advisor：Fu-Yu Tsai Keywords : mesoporous material, palladium complex, recyclable catalyst, Stille coupling The palladium catalyzed cross-coupling of organotin compounds with aryl halides has appeared as one of the most significant
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Book chapters on the topic "Stille coupling reactions"

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Li, Jie Jack. "Stille coupling." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_276.

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Li, Jie Jack. "Stille coupling." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_246.

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Li, Jie Jack. "Stille coupling." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_264.

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Li, Jie Jack. "Stille coupling." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_288.

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Li, Jie Jack. "Stille Coupling." In Name Reactions. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_145.

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Banerjee, Abhinandan, and Robert W. J. Scott. "Nanocatalysts for Hiyama, Stille, Kumada, and Negishi C-C Coupling Reactions." In Nanocatalysis Synthesis and Applications. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118609811.ch5.

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Abe, M., and T. Yamamoto. "Stille Coupling Reactions." In Monocyclic Arenes, Quasiarenes, and Annulenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-045-00587.

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Milata, V., S. Rádl, and S. Voltrová. "Stille Coupling Reactions." In X-Ene-X (X=F, Cl, Br, I, O, S, Se, Te, N, P), Ene-Hal, and Ene-O Compounds. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-032-00714.

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Sato, N. "Stille Cross-Coupling Reaction and Related Reactions." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-116-00480.

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Schatz, J., and M. Seler. "Palladium-Catalyzed Stille Cross-Coupling Reactions." In Fully Unsaturated Small-Ring Heterocycles and Monocyclic Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-109-00263.

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Conference papers on the topic "Stille coupling reactions"

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Levashov, Andrey, Dmitriy Buriy, Valeriy Konshin, and Alexey Andreev (deceased). "Stille-type cross coupling reactions with tetraalkynyl stannanes." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a060.

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Habonimana, Pascal, Sven Claessens, and Norbert De Kimpe. "The Use of the Stille Cross-Coupling Reaction in the Prenylation of Naphthoquinones." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01485.

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Cartellier, Alain. "Strong Coupling in Laminar Bubbly Flows and Related Modeling Issues." In ASME 2002 Joint U.S.-European Fluids Engineering Division Conference. ASMEDC, 2002. http://dx.doi.org/10.1115/fedsm2002-31383.

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Systems involving swarms of bubbles in an otherwise laminar continuous phase are common in industrial processes. In some cases, the gas is injected to ensure a given chemical reaction (bubble columns in oil industry) or to sustain a biochemical process (aeration tanks in waste water treatment plants). Gas inclusions can also appear due to the reaction itself (electrolysis cells, anaerobic digestion). In others circumstances, the gas phase is chemically passive and it is introduced mainly to favor mixing and/or separation (flotation devices). In these processes, it is desirable to access parame
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Chen, Lu, and Francine Battaglia. "Computational Study Comparing Reduced Chemical Mechanisms With the PDF Method in Non-Premixed Flames." In ASME 2016 Fluids Engineering Division Summer Meeting collocated with the ASME 2016 Heat Transfer Summer Conference and the ASME 2016 14th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/fedsm2016-7543.

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Reactive flow simulations involving turbulence-chemistry interactions can be very challenging because of the strong non-linear coupling between chemistry and fluid dynamics. Furthermore, the chemistry is described with hundreds of reactions, which is prohibitive to solve using computational fluid dynamics (CFD). Using a reduced set of mechanisms that contains a subset of the important species is more practical. However, the species modeled must capture the key combustion characteristics of interest, such as ignition, species distributions and major pollutant formation. Previously, the authors
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Jacobsen, Katja, and Gu¨nther F. Clauss. "Time-Domain Simulations of Multi-Body Systems in Deterministic Wave Trains." In 25th International Conference on Offshore Mechanics and Arctic Engineering. ASMEDC, 2006. http://dx.doi.org/10.1115/omae2006-92348.

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A growing amount of reports on heavy lift operations involving huge crane vessels prove that investigations on the motion behavior of multi-body systems are vital regarding the combined aspects of safety and economics. In this paper a method of transforming frequency-domain into time-domain results is presented. With the panel program WAMIT (WAMIT Inc.) the Response Amplitude Operators (RAO) of the motions in six degrees of freedom of the structures involved in a lift operation are calculated. The multi-bodies RAOs differ significantly from those of the single structures (without interaction e
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Griffiths, Terry, and Wenwen Shen. "Further Development and Benchmarking of a Novel Pipe-Soil Interaction Model for Subsea Pipeline Design." In ASME 2013 32nd International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/omae2013-10621.

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For well over a decade it has been widely recognised that our existing models and tools for subsea pipeline stability design fail to account for the fact that seabed soils tend to become mobile well before the onset of pipeline instability. Despite ample evidence obtained from both laboratory and field observations that sediment mobility has a key role to play in understanding pipeline/soil interaction, no models have been presented previously which account for the tripartite interaction between the fluid and the pipe, the fluid and the soil, and the pipe and the soil. This paper presents furt
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Wang, Gaofeng, Dimitrios Papadogiannis, Florent Duchaine, Nicolas Gourdain, and Laurent Y. M. Gicquel. "Towards Massively Parallel Large Eddy Simulation of Turbine Stages." In ASME Turbo Expo 2013: Turbine Technical Conference and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/gt2013-94852.

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The context of integrated numerical simulations of gas turbine engines by use of high-fidelity Computational Fluid Dynamic (CFD) tools recently emerged as a promising path to improve engines design and understanding. Relying on massively parallel super-computing such propositions still have to prove feasibility to efficiently take advantage of the ever increasing computing power made available worldwide. Although Large Eddy Simulation (LES) has recently proven its superiority in the context of the combustion chamber of gas turbine, methodologies need to be developed and start addressing the pr
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