Добірка наукової літератури з теми "Copper catalyzed synthesis"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Copper catalyzed synthesis".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Copper catalyzed synthesis"
Yus, Miguel. "Copper-Catalyzed Asymmetric Synthesis." Current Organic Chemistry 18, no. 15 (September 16, 2014): 2047. http://dx.doi.org/10.2174/138527281815140916093030.
Повний текст джерелаLiu, Nan, Bo Wang, Wenwen Chen, Chulong Liu, Xinyan Wang, and 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, no. 93 (2014): 51133–39. http://dx.doi.org/10.1039/c4ra09593f.
Повний текст джерелаDepa, Navaneetha, and Harikrishna Erothu. "DESIGN AND SYNTHESIS OF NOVEL PERILLYL-4HPYRANTRIAZOLE DERIVATIVES." Rasayan Journal of Chemistry 15, no. 01 (2022): 302–9. http://dx.doi.org/10.31788/rjc.2022.1516629.
Повний текст джерелаRoke, D., M. Fañanás-Mastral, and B. L. Feringa. "Iterative catalyst controlled diastereodivergent synthesis of polypropionates." Organic Chemistry Frontiers 3, no. 11 (2016): 1383–91. http://dx.doi.org/10.1039/c6qo00199h.
Повний текст джерелаHemming, David, Russell Fritzemeier, Stephen A. Westcott, Webster L. Santos, and Patrick G. Steel. "Copper-boryl mediated organic synthesis." Chemical Society Reviews 47, no. 19 (2018): 7477–94. http://dx.doi.org/10.1039/c7cs00816c.
Повний текст джерелаLu, Jiaqing, Yuning Man, Yabin Zhang, Bo Lin, Qi Lin, and Zhiqiang Weng. "Copper-catalyzed chemoselective synthesis of 4-trifluoromethyl pyrazoles." RSC Advances 9, no. 53 (2019): 30952–56. http://dx.doi.org/10.1039/c9ra07694h.
Повний текст джерелаBates, Craig G., Pranorm Saejueng, and D. Venkataraman. "Copper-Catalyzed Synthesis of 1,3-Enynes." Organic Letters 6, no. 9 (April 2004): 1441–44. http://dx.doi.org/10.1021/ol049706e.
Повний текст джерелаAllen, Derek Van, and D. Venkataraman. "Copper-Catalyzed Synthesis of Unsymmetrical Triarylphosphines†." Journal of Organic Chemistry 68, no. 11 (May 2003): 4590–93. http://dx.doi.org/10.1021/jo0343376.
Повний текст джерелаZheng, Nan, and Stephen L. Buchwald. "Copper-Catalyzed Regiospecific Synthesis ofN-Alkylbenzimidazoles." Organic Letters 9, no. 23 (November 2007): 4749–51. http://dx.doi.org/10.1021/ol7020737.
Повний текст джерелаJen, Wendy S., Matthew D. Truppo, Deborah Amos, Paul Devine, Michael McNevin, Mirlinda Biba, and Kevin R. Campos. "Copper-Catalyzed Synthesis of Enantioenriched Tetraarylethanes." Organic Letters 10, no. 5 (March 2008): 741–44. http://dx.doi.org/10.1021/ol7027543.
Повний текст джерелаДисертації з теми "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.
Повний текст джерелаChapter 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.
Повний текст джерелаCataloged 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.
Повний текст джерелаChapter 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.
Повний текст джерелаMeng, 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.
Повний текст джерелаChapter 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.
Повний текст джерелаMcIntosh, 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.
Повний текст джерелаOu, Jun, and 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.
Повний текст джерелаpublished_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.
Повний текст джерелаLonca, 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.
Повний текст джерелаThis 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
Книги з теми "Copper catalyzed synthesis"
Alexakis, Alexandre, Norbert Krause, and Simon Woodward, eds. Copper-Catalyzed Asymmetric Synthesis. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.
Повний текст джерелаOhta, Yusuke. Copper-catalyzed multi-component reactions: Synthesis of nitrogen-containing polycyclic compounds. Berlin: Springer Verlag, 2011.
Знайти повний текст джерелаWoodward, Simon, Norbert Krause, and Alexandre Alexakis. Copper-Catalyzed Asymmetric Synthesis. Wiley & Sons, Incorporated, John, 2013.
Знайти повний текст джерелаWoodward, Simon, Norbert Krause, and Alexandre Alexakis. Copper-Catalyzed Asymmetric Synthesis. Wiley & Sons, Incorporated, John, 2013.
Знайти повний текст джерелаWoodward, Simon, Norbert Krause, and Alexandre Alexakis. Copper-Catalyzed Asymmetric Synthesis. Wiley & Sons, Limited, John, 2014.
Знайти повний текст джерелаWoodward, Simon, Norbert Krause, and Alexandre Alexakis. Copper-Catalyzed Asymmetric Synthesis. Wiley & Sons, Incorporated, John, 2013.
Знайти повний текст джерелаOhta, Yusuke. Copper-Catalyzed Multi-Component Reactions: Synthesis of Nitrogen-Containing Polycyclic Compounds. Springer, 2011.
Знайти повний текст джерелаOhta, Yusuke. Copper-Catalyzed Multi-Component Reactions: Synthesis of Nitrogen-Containing Polycyclic Compounds. Springer, 2013.
Знайти повний текст джерелаFu, S. S. B. Surface science studies of catalyzed methanol synthesis model copper and Cu-Zn-O surfaces. Lawrence BerkeleyLab., 1991.
Знайти повний текст джерелаЧастини книг з теми "Copper catalyzed synthesis"
Alexakis, Alexandre, Norbert Krause, and Simon Woodward. "Introduction." In Copper-Catalyzed Asymmetric Synthesis, 1–2. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch.
Повний текст джерелаWoodward, Simon. "The Primary Organometallic in Copper-Catalyzed Reactions." In Copper-Catalyzed Asymmetric Synthesis, 3–32. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch1.
Повний текст джерелаDidier, Dorian, and Ilan Marek. "Carbometallation Reactions." In Copper-Catalyzed Asymmetric Synthesis, 267–82. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch10.
Повний текст джерелаAdachi, Shinya, Ramkumar Moorthy, and Mukund P. Sibi. "Chiral Copper Lewis Acids in Asymmetric Transformations." In Copper-Catalyzed Asymmetric Synthesis, 283–324. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch11.
Повний текст джерелаLarsson, Per-Fredrik, Per-Ola Norrby, and Simon Woodward. "Mechanistic Aspects of Copper-Catalyzed Reactions." In Copper-Catalyzed Asymmetric Synthesis, 325–52. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch12.
Повний текст джерелаvon Rekowski, Felicitas, Carina Koch, and Ruth M. Gschwind. "NMR Spectroscopic Aspects." In Copper-Catalyzed Asymmetric Synthesis, 353–72. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch13.
Повний текст джерелаCalvo, Beatriz C., Jeffrey Buter, and Adriaan J. Minnaard. "Applications to the Synthesis of Natural Products." In Copper-Catalyzed Asymmetric Synthesis, 373–448. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch14.
Повний текст джерелаAlexakis, Alexandre, Norbert Krause, and Simon Woodward. "Copper-Catalyzed Asymmetric Conjugate Addition." In Copper-Catalyzed Asymmetric Synthesis, 33–68. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch2.
Повний текст джерелаTissot, Matthieu, Hailing Li, and Alexandre Alexakis. "Copper-Catalyzed Asymmetric Conjugate Addition and Allylic Substitution of Organometallic Reagents to Extended Multiple-Bond Systems." In Copper-Catalyzed Asymmetric Synthesis, 69–84. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch3.
Повний текст джерелаBaslé, Olivier, Audrey Denicourt-Nowicki, Christophe Crévisy, and Marc Mauduit. "Asymmetric Allylic Alkylation." In Copper-Catalyzed Asymmetric Synthesis, 85–126. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664573.ch4.
Повний текст джерелаТези доповідей конференцій з теми "Copper catalyzed synthesis"
Limberger, Jones, and Adriano Lisboa Monteiro. "Copper Catalyzed C-O and C-N Coupling of Vinyl Bromides with Phenols and Azoles." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0149-1.
Повний текст джерелаBraga, Antonio Luiz, Syed M. Salman, Sayyar Muhamamd, Oscar E. D. Rodrigues, Luciano Dornelles, and Ricardo S. Schwab. "Copper Oxide Nanoparticles-Catalyzed Aziridine Ring Opening with Diaryl Diselenides Under Ionic Liquid as Reaction Medium." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0026-1.
Повний текст джерелаSeus, Natália, Maiara T. Saraiva, Eder J. Lenardão, Gelson Perin, Raquel G. Jacob, Samuel R. Mendes, and Diego Alves. "Synthesis of Arylseleno-1,2,3-triazoles via Copper Catalyzed 1,3-Dipolar Cycloadditions of Arylseleno Azides with Alkynes." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0100-1.
Повний текст джерелаNunes, Vanessa Lóren, (PG) Ingryd Cristina de Oliveira, and Olga S. do Rêgo Barros. "Copper(I)-Senelenophene-2-carboxylate Catalyzed Cross- Coupling of Aryl or alkyl Thiols And Aryl Halides." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0177-1.
Повний текст джерелаSeus, Natália, Maiara T. Saraiva, Caroline C. Schneider, Eder J. Lenardão, Gelson Perin, Raquel G. Jacob, Samuel R. Mendes, and Diego Alves. "Synthesis of Arylseleno-1,2,3-triazoles via Copper Catalyzed 1,3-Dipolar Cycloadditions of Arylseleno Azides with Alkynes." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0231-1.
Повний текст джерелаGodoi, Marcelo, Eduardo Wronscki Ricardo, Tiago Elias Frizon, Devender Singh, and Antonio Luiz Braga. "An Efficient Synthesis of Alkynyl Selenides and Telurides from Terminal Acetylenes and Diorganoyl Dichalcogenides Catalyzed by Copper Oxide Nanopowder." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0115-1.
Повний текст джерелаGalindo, Christophe, Françoise Soyer, and Pierre Le Barny. "Copper(I)-catalyzed azide-alkyne cycloaddition for the synthesis of nonlinear electro-optic side-chain copolymers." In Security + Defence, edited by Colin Lewis, Douglas Burgess, Roberto Zamboni, François Kajzar, and Emily M. Heckman. SPIE, 2010. http://dx.doi.org/10.1117/12.864232.
Повний текст джерелаLin, T. Y., Y. L. Chen, C. W. Huang, C. F. Chang, C. H. Chiu, G. M. Huang, Y. C. Lo, and W. W. Wu. "In situ investigation of self-catalyzed purity Copper nanowire growth through seed-mediated synthesis." In 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.
Повний текст джерелаRukmini, Elisabeth, and Richard Taylor. "Microwave Assistance in the Copper-Catalyzed Reactions of Aliphatic Alcohols with Aryl Iodides." In The 13th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00158.
Повний текст джерелаRamasami, Ponnadurai, Hanusha Bhakhoa, and Lydia Rhyman. "Copper(I) Catalyzed [3+2] Cycloaddition Reaction with Mechanistic Disparity: A DFT Study." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-e017.
Повний текст джерела