Literatura académica sobre el tema "Copper catalyzed synthesis"
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Artículos de revistas sobre el tema "Copper catalyzed synthesis"
Yus, Miguel. "Copper-Catalyzed Asymmetric Synthesis". Current Organic Chemistry 18, n.º 15 (16 de septiembre de 2014): 2047. http://dx.doi.org/10.2174/138527281815140916093030.
Texto completoLiu, Nan, Bo Wang, Wenwen Chen, Chulong Liu, Xinyan Wang y Yuefei Hu. "A general route for synthesis of N-aryl phenoxazines via copper(i)-catalyzed N-, N-, and O-arylations of 2-aminophenols". RSC Adv. 4, n.º 93 (2014): 51133–39. http://dx.doi.org/10.1039/c4ra09593f.
Texto completoDepa, Navaneetha y Harikrishna Erothu. "DESIGN AND SYNTHESIS OF NOVEL PERILLYL-4HPYRANTRIAZOLE DERIVATIVES". Rasayan Journal of Chemistry 15, n.º 01 (2022): 302–9. http://dx.doi.org/10.31788/rjc.2022.1516629.
Texto completoRoke, D., M. Fañanás-Mastral y B. L. Feringa. "Iterative catalyst controlled diastereodivergent synthesis of polypropionates". Organic Chemistry Frontiers 3, n.º 11 (2016): 1383–91. http://dx.doi.org/10.1039/c6qo00199h.
Texto completoHemming, David, Russell Fritzemeier, Stephen A. Westcott, Webster L. Santos y Patrick G. Steel. "Copper-boryl mediated organic synthesis". Chemical Society Reviews 47, n.º 19 (2018): 7477–94. http://dx.doi.org/10.1039/c7cs00816c.
Texto completoLu, Jiaqing, Yuning Man, Yabin Zhang, Bo Lin, Qi Lin y Zhiqiang Weng. "Copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles". RSC Advances 9, n.º 53 (2019): 30952–56. http://dx.doi.org/10.1039/c9ra07694h.
Texto completoBates, Craig G., Pranorm Saejueng y D. Venkataraman. "Copper-Catalyzed Synthesis of 1,3-Enynes". Organic Letters 6, n.º 9 (abril de 2004): 1441–44. http://dx.doi.org/10.1021/ol049706e.
Texto completoAllen, Derek Van y D. Venkataraman. "Copper-Catalyzed Synthesis of Unsymmetrical Triarylphosphines†". Journal of Organic Chemistry 68, n.º 11 (mayo de 2003): 4590–93. http://dx.doi.org/10.1021/jo0343376.
Texto completoZheng, Nan y Stephen L. Buchwald. "Copper-Catalyzed Regiospecific Synthesis ofN-Alkylbenzimidazoles". Organic Letters 9, n.º 23 (noviembre de 2007): 4749–51. http://dx.doi.org/10.1021/ol7020737.
Texto completoJen, Wendy S., Matthew D. Truppo, Deborah Amos, Paul Devine, Michael McNevin, Mirlinda Biba y Kevin R. Campos. "Copper-Catalyzed Synthesis of Enantioenriched Tetraarylethanes". Organic Letters 10, n.º 5 (marzo de 2008): 741–44. http://dx.doi.org/10.1021/ol7027543.
Texto completoTesis sobre el tema "Copper catalyzed synthesis"
Black, Daniel. "Imines in copper-catalyzed cross-coupling reactions". Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=102960.
Texto completoChapter 2 of this thesis describes a new copper-catalyzed multicomponent synthesis of alpha-substituted amides. This reaction was developed based upon previous work in this laboratory, which showed that palladium catalysts were competent in Stille-type cross-coupling of imines, acid chlorides, and organostannanes. While providing a mild method of generating the amide products, a more general procedure able to incorporate a wider range of organostannanes was sought. This chapter details the development of a copper-catalyzed protocol, which, as well as performing the cross-coupling under mild reaction conditions, proceeds with a diverse range of aryl-, heteroaryl-, and vinyl-substituted organostannanes and employs an inexpensive and readily available catalyst. Through this system, control over regioselectivity of addition to alpha,beta-unsaturated imines is also possible.
Chapter 3 demonstrates that, in addition to organostannanes, other substrates are viable in copper-catalyzed cross-coupling with imines and acid chlorides. Herein, the coupling of terminal alkynes with imines and acid chlorides is described, leading to an efficient synthesis of tertiary propargylamides directly from simple starting materials. This synthesis incorporates a wide variety of substituted imines, acid chlorides/chloroformates, and terminal alkynes, providing a rapid synthesis of these useful building blocks (reaction completion in only 15 minutes). In addition, the process is shown to work with aza-aromatic heterocycles, such as pyridine, where the alkynylation occurs exclusively at the 2-position.
Chapter 4 describes the utility of these rapid multicomponent reactions, where the products are directly converted into oxazole heterocycles. Copper-catalyzed- and zinc-catalyzed protocols are developed for the synthesis of secondary propargylamides from silyl-imines, acid chlorides, and terminal alkynes. The secondary propargylamide products are then, in a one pot sequence, transformed into trisubstituted oxazoles.
Chapter 5 describes the development of an atom-economical, non-toxic alternative to the organotin coupling described in Chapter 2. This involves the use of tri- and tetraorgano-indium reagents, which can transfer all of their organic groups in a copper-catalyzed coupling with imines and acid chlorides. This reaction shows good functional group compatibility and further expands the scope of alpha-substituted amides and N-protected amines that can be synthesized through mild copper catalysis.
Chapter 6 explores the enantioselective alkynylation of nitrogen-containing heterocycles. As described in Chapter 3, heterocycles such as pyridine can undergo copper-catalyzed 1,2-addition with terminal alkynes upon activation by chloroformates. As this process generates a stereocenter, it is possible to introduce enantio-control into the reactions by using a chiral copper catalyst. With ligands from the PINAP series, enantioselectivities of up to 84% can be induced in the coupling of nitrogen-containing heterocycles (e.g., quinoline), chloroformates, and terminal alkynes. This provides a mild and simple synthesis of chiral 2-alkynyl-1,2-dihydroquinolines directly from simple starting materials.
Wong, Zackary L. (Zackary Leland). "Copper-catalyzed enantioselective stereodivergent synthesis of amino alcohols". Thesis, Massachusetts Institute of Technology, 2016. http://hdl.handle.net/1721.1/103506.
Texto completoCataloged from PDF version of thesis.
Includes bibliographical references (pages 46-50 (first group)).
Different stereoisomers of bioactive molecules can have distinct activities in biological systems. For this reason, it is routine procedure in the drug discovery and development process to prepare the full matrix of possible stereoisomers of drug candidates for biological evaluation and to determine the stereochemical purity of these molecules. Despite many recent advances in asymmetric synthesis, the development of general and practical strategies that are fully divergent and give rise to all stereoisomers of products bearing multiple contiguous stereocenters remains a significant challenge. Herein we report a stereodivergent copper-based approach for the expeditious construction of amino alcohols with high levels of chemo-, regio-, diastero- and enantioselectivity. Specifically, these amino alcohol products were synthesized using the sequential copper hydride-catalyzed hydrosilylation and hydroamination of readily available enals and enones. This strategy provides a route to all possible stereoisomers of these amino alcohol products, which contain up to three contiguous stereocenters. Catalyst control and stereospecificity were simultaneously leveraged to attain exceptional control of the product stereochemistry. Beyond the utility of this protocol, the strategy demonstrated here should inspire the development of methods providing complete sets of stereoisomers for other valuable synthetic targets.
by Zackary L. Wong.
S.M.
Huang, Zeyu. "Synthesis of Multifunctional Organoboron Compounds by Copper-Catalyzed Enantioselective Reactions:". Thesis, Boston College, 2017. http://hdl.handle.net/2345/bc-ir:107346.
Texto completoChapter 1. We have developed a catalytic method for enantio- and SN2’-selective allylic substitution of commercially available diborylmethane to trisubstituted allylic phosphates (pin = pinacolato). The transformations are catalyzed by NHC–Cu complexes (NHC = N-heterocyclic carbene). Products bearing quaternary stereogenic carbon centers are obtained in up to 86% yield (after oxidation), >98:2 SN2’/SN2 selectivity and 95:5 enantiomeric ratio (e.r.). Chapter 2. We have developed a facile multicomponent catalytic process that begins with a chemo- and site-selective copper–hydride addition to allenyl-B(pin) followed by enantioselective conjugate addition of the resulting allylcopper intermediate to α,β-unsaturated malonate, generating products that contain a stereogenic center and an easily functionalizable alkenyl-B(pin) group in up to 84% yield, >98:2 E/Z selectivity and 96:4 enantiomeric ratio. The transformations are catalyzed by chiral Cu complexes derived from commercially available bisphosphines and CuCl
Thesis (MS) — Boston College, 2017
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Takeda, Momotaro. "Copper-Catalyzed Asymmetric Allylic Substitution with Organo- and Silylboronates". 京都大学 (Kyoto University), 2014. http://hdl.handle.net/2433/188504.
Texto completoMeng, Fanke. "Design of Copper-Catalyzed Multicomponent Reactions and Applications to Natural Product Synthesis". Thesis, Boston College, 2015. http://hdl.handle.net/2345/bc-ir:104876.
Texto completoChapter 1. Ligand-Controlled Site-Selective NHC–Cu-Catalyzed Protoboration of Monosubstituted Allenes. Site-selective proto–boryl additions to monosubstituted allenes promoted by NHC–Cu complexes are disclosed. Synthetically useful 1,1-disubstituted and Z-trisubstituted alkenylboron compounds are afforded in high efficiency (71%–92% yield) and site selectivity (88% to >98%) through proper choice of NHC ligands. Mechanistic study with the assistance of DFT calculations indicates that protonation of 2-boron-substituted allylcopper complex occurs through six-membered cyclic transition state. The utility of this protocol is demonstrated through application to fragment synthesis of an antibiotic macrolide natural product elansolid A. Chapter 2. Cu-Catalyzed Chemoselective Copper–Boron Additions to Monosubstituted Allenes Followed by Allyl Additions to Carbonyl Compounds. The first examples of catalytic generation of 2-boron-substituted allylcopper species and their in situ use for C–C bond formation are described. The reactions are performed in the presence of bisphosphine– or NHC–Cu complexes at 22 oC. High-value alcohol-containing alkenylboron compounds are provided in high efficiency (68–92% yield after oxidation) and stereoselectivity (88:12 to >98:2 dr). The reactions proceed with exclusive γ-addition mode through a cyclic six-membered transition state. Enantioselectivity can be achieved with chiral bisphosphine ligands in up to 97:3 enantiomeric ratio. Chapter 3. Chemo-, Site- and Enantioselective Copper–Boron Additions to 1,3-Enynes Followed by Site- and Diastereoselective Additions of the Resulting Allenylcopper Complexes to Aldehydes. Catalytic enantioselective multicomponent reactions involving 1,3-enynes, aldehydes and B2(pin)2 are described. The resulting products contain a primary C–B(pin) bond, as well as alkyne- and hydroxyl-substituted tertiary stereogenic centers. A critical feature is high enantioselectivity of the initial Cu–B addition to an alkyne-substituted terminal alkene. The key mechanistic issues are investigated by DFT calculations. Reactions are promoted in the presence of the Cu complex of an enantiomerically pure C1-symmetric bisphosphine and are complete in 8 h at ambient temperature. Products are generated in 66–94% yield (after oxidation or catalytic cross-coupling), 90:10 to >98:2 diastereomeric ratio, and 85:15–99:1 enantiomeric ratio. Aryl-, heteroaryl-, alkenyl-, and alkyl-substituted aldehydes and enynes are suitable substrates. Utility is demonstrated through catalytic alkylation and arylation of the organoboron compounds as well as applications to synthesis of fragments of tylonolide and mycinolide IV. Chapter 4. Multifunctional Alkenylboron Compounds through Single-Catalyst-Controlled Multicomponent Reactions and Their Applications in Scalable Natural Product Synthesis. A facile multicomponent catalytic process that begins with a chemo-, site- and diastereoselective copper–boron addition to a monosubstituted allene followed by addition of the resulting boron-substituted organocopper intermediate to an allylic phosphate, generating products that contain a stereogenic center, a monosubstituted alkene and an easily functionalizable Z-trisubstituted alkenylboron group in up to 89% yield with >98% branch selectivity and stereoselectivity and an enantiomeric ratio greater than 99:1. The copper-based catalyst is derived from a robust heterocyclic salt that can be prepared in multigram quantities from inexpensive starting materials and without costly column chromatography purification. The utility of the method is demonstrated through enantioselective synthesis of gram quantities of two natural products, rottnestol and herboxidiene/GEX1A. Chapter 5. Cu-Catalyzed Enantioselective Allyl and Propargyl 1,6-Conjugate Additions through 3,3’-Reductive Elimination. Catalytic enantioselective 1,6-conjugate additions of allyl-type nucleophiles promoted by NHC–Cu complexes are reported. Propargyl and 2-boron allyl 1,6-conjugate products are formed in high efficiency, diastereo- and enantioselectivity. The unique mechanistic feature is that the transformations proceed through Cu-catalyzed 3,3’-reductive elimination, that is unprecedented for copper catalysis. Further mechanistic study and application to complex molecule synthesis will be conducted
Thesis (PhD) — Boston College, 2015
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Dong, Wanrong [Verfasser]. "Rhodium-catalyzed direct C-H functionalizations of sulfoximines and copper-catalyzed enantioselective synthesis of dihydropyrazoles / Wanrong Dong". Aachen : Hochschulbibliothek der Rheinisch-Westfälischen Technischen Hochschule Aachen, 2014. http://d-nb.info/1057036587/34.
Texto completoMcIntosh, Melissa Clark Timothy B. "Copper-catalyzed diboration of ketones : facile synthesis of tertiary a-Hydroxyboronate esters /". Online version, 2010. http://content.wwu.edu/cdm4/item_viewer.php?CISOROOT=/theses&CISOPTR=336&CISOBOX=1&REC=11.
Texto completoOu, Jun y 欧军. "Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B47849708.
Texto completopublished_or_final_version
Chemistry
Doctoral
Doctor of Philosophy
Ota, Yusuke. "Synthesis of Nitrogen-Containing Polycyclic Compounds through Copper-Catalyzed Multi-Component Reaction". 京都大学 (Kyoto University), 2010. http://hdl.handle.net/2433/120509.
Texto completoLonca, Geoffroy. "Development of new reactions of organic synthesis catalyzed by gold and copper". Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLX057/document.
Texto completoThis manuscript presents the development of gold- and copper-catalyzed methods for the synthesis of heterocyclic compounds and trifluoromethylated products.Firstly, a gold-catalyzed synthesis of trifluoromethyl allenes was developed, relying on a 1,5 hydride shift. This method allows to access, in a very efficient and selective way, a large range of perfluoroalkylated allenes, of which the synthetic potential was also demonstrated.Afterwards, the catalytic power of gold was then used in a synthesis of 2H-1,3-oxazines, relying on a 6-endo type cyclization of azide-yne substrates. This methods allows to access, in very mild condition, an unprecedently large range of polysubstituted oxazines in excellent yields.Finally, a method for the copper-catalyzed radical hydrofunctionalization of alkenols was developed. The strategy involved relies on a 1,5 hydrogen abstraction, in which a benzyloxy moiety plays the role of the hydrogen donor
Libros sobre el tema "Copper catalyzed synthesis"
Alexakis, Alexandre, Norbert Krause y Simon Woodward, eds. Copper-Catalyzed Asymmetric Synthesis. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.
Texto completoOhta, Yusuke. Copper-catalyzed multi-component reactions: Synthesis of nitrogen-containing polycyclic compounds. Berlin: Springer Verlag, 2011.
Buscar texto completoWoodward, Simon, Norbert Krause y Alexandre Alexakis. Copper-Catalyzed Asymmetric Synthesis. Wiley & Sons, Incorporated, John, 2013.
Buscar texto completoWoodward, Simon, Norbert Krause y Alexandre Alexakis. Copper-Catalyzed Asymmetric Synthesis. Wiley & Sons, Incorporated, John, 2013.
Buscar texto completoWoodward, Simon, Norbert Krause y Alexandre Alexakis. Copper-Catalyzed Asymmetric Synthesis. Wiley & Sons, Limited, John, 2014.
Buscar texto completoWoodward, Simon, Norbert Krause y Alexandre Alexakis. Copper-Catalyzed Asymmetric Synthesis. Wiley & Sons, Incorporated, John, 2013.
Buscar texto completoOhta, Yusuke. Copper-Catalyzed Multi-Component Reactions: Synthesis of Nitrogen-Containing Polycyclic Compounds. Springer, 2011.
Buscar texto completoOhta, Yusuke. Copper-Catalyzed Multi-Component Reactions: Synthesis of Nitrogen-Containing Polycyclic Compounds. Springer, 2013.
Buscar texto completoFu, S. S. B. Surface science studies of catalyzed methanol synthesis model copper and Cu-Zn-O surfaces. Lawrence BerkeleyLab., 1991.
Buscar texto completoCapítulos de libros sobre el tema "Copper catalyzed synthesis"
Alexakis, Alexandre, Norbert Krause y Simon Woodward. "Introduction". En Copper-Catalyzed Asymmetric Synthesis, 1–2. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch.
Texto completoWoodward, Simon. "The Primary Organometallic in Copper-Catalyzed Reactions". En Copper-Catalyzed Asymmetric Synthesis, 3–32. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch1.
Texto completoDidier, Dorian y Ilan Marek. "Carbometallation Reactions". En Copper-Catalyzed Asymmetric Synthesis, 267–82. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch10.
Texto completoAdachi, Shinya, Ramkumar Moorthy y Mukund P. Sibi. "Chiral Copper Lewis Acids in Asymmetric Transformations". En Copper-Catalyzed Asymmetric Synthesis, 283–324. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch11.
Texto completoLarsson, Per-Fredrik, Per-Ola Norrby y Simon Woodward. "Mechanistic Aspects of Copper-Catalyzed Reactions". En Copper-Catalyzed Asymmetric Synthesis, 325–52. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch12.
Texto completovon Rekowski, Felicitas, Carina Koch y Ruth M. Gschwind. "NMR Spectroscopic Aspects". En Copper-Catalyzed Asymmetric Synthesis, 353–72. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch13.
Texto completoCalvo, Beatriz C., Jeffrey Buter y Adriaan J. Minnaard. "Applications to the Synthesis of Natural Products". En Copper-Catalyzed Asymmetric Synthesis, 373–448. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch14.
Texto completoAlexakis, Alexandre, Norbert Krause y Simon Woodward. "Copper-Catalyzed Asymmetric Conjugate Addition". En Copper-Catalyzed Asymmetric Synthesis, 33–68. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch2.
Texto completoTissot, Matthieu, Hailing Li y Alexandre Alexakis. "Copper-Catalyzed Asymmetric Conjugate Addition and Allylic Substitution of Organometallic Reagents to Extended Multiple-Bond Systems". En Copper-Catalyzed Asymmetric Synthesis, 69–84. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch3.
Texto completoBaslé, Olivier, Audrey Denicourt-Nowicki, Christophe Crévisy y Marc Mauduit. "Asymmetric Allylic Alkylation". En Copper-Catalyzed Asymmetric Synthesis, 85–126. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch4.
Texto completoActas de conferencias sobre el tema "Copper catalyzed synthesis"
Limberger, Jones y Adriano Lisboa Monteiro. "Copper Catalyzed C-O and C-N Coupling of Vinyl Bromides with Phenols and Azoles". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0149-1.
Texto completoBraga, Antonio Luiz, Syed M. Salman, Sayyar Muhamamd, Oscar E. D. Rodrigues, Luciano Dornelles y Ricardo S. Schwab. "Copper Oxide Nanoparticles-Catalyzed Aziridine Ring Opening with Diaryl Diselenides Under Ionic Liquid as Reaction Medium". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0026-1.
Texto completoSeus, Natália, Maiara T. Saraiva, Eder J. Lenardão, Gelson Perin, Raquel G. Jacob, Samuel R. Mendes y Diego Alves. "Synthesis of Arylseleno-1,2,3-triazoles via Copper Catalyzed 1,3-Dipolar Cycloadditions of Arylseleno Azides with Alkynes". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0100-1.
Texto completoNunes, Vanessa Lóren, (PG) Ingryd Cristina de Oliveira y Olga S. do Rêgo Barros. "Copper(I)-Senelenophene-2-carboxylate Catalyzed Cross- Coupling of Aryl or alkyl Thiols And Aryl Halides". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0177-1.
Texto completoSeus, Natália, Maiara T. Saraiva, Caroline C. Schneider, Eder J. Lenardão, Gelson Perin, Raquel G. Jacob, Samuel R. Mendes y Diego Alves. "Synthesis of Arylseleno-1,2,3-triazoles via Copper Catalyzed 1,3-Dipolar Cycloadditions of Arylseleno Azides with Alkynes". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0231-1.
Texto completoGodoi, Marcelo, Eduardo Wronscki Ricardo, Tiago Elias Frizon, Devender Singh y Antonio Luiz Braga. "An Efficient Synthesis of Alkynyl Selenides and Telurides from Terminal Acetylenes and Diorganoyl Dichalcogenides Catalyzed by Copper Oxide Nanopowder". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0115-1.
Texto completoGalindo, Christophe, Françoise Soyer y Pierre Le Barny. "Copper(I)-catalyzed azide-alkyne cycloaddition for the synthesis of nonlinear electro-optic side-chain copolymers". En Security + Defence, editado por Colin Lewis, Douglas Burgess, Roberto Zamboni, François Kajzar y Emily M. Heckman. SPIE, 2010. http://dx.doi.org/10.1117/12.864232.
Texto completoLin, T. Y., Y. L. Chen, C. W. Huang, C. F. Chang, C. H. Chiu, G. M. Huang, Y. C. Lo y W. W. Wu. "In situ investigation of self-catalyzed purity Copper nanowire growth through seed-mediated synthesis". En 2017 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2017. http://dx.doi.org/10.7567/ssdm.2017.ps-8-04.
Texto completoRukmini, Elisabeth y Richard Taylor. "Microwave Assistance in the Copper-Catalyzed Reactions of Aliphatic Alcohols with Aryl Iodides". En The 13th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00158.
Texto completoRamasami, Ponnadurai, Hanusha Bhakhoa y Lydia Rhyman. "Copper(I) Catalyzed [3+2] Cycloaddition Reaction with Mechanistic Disparity: A DFT Study". En The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-e017.
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