Добірка наукової літератури з теми "Carbon-heteroatom Bond Forming Reactions"
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Статті в журналах з теми "Carbon-heteroatom Bond Forming Reactions"
Corma, A., A. Leyva-Pérez, and Maria J. Sabater. "Gold-Catalyzed Carbon−Heteroatom Bond-Forming Reactions." Chemical Reviews 111, no. 3 (March 9, 2011): 1657–712. http://dx.doi.org/10.1021/cr100414u.
Повний текст джерелаLumb, Jean-Philip, and Kenneth Esguerra. "Cu(III)-Mediated Aerobic Oxidations." Synthesis 51, no. 02 (December 3, 2018): 334–58. http://dx.doi.org/10.1055/s-0037-1609635.
Повний текст джерелаTakemoto, Yoshiji, and Hideto Miyabe. "ChemInform Abstract: Asymmetric Carbon-Heteroatom Bond-Forming Reactions." ChemInform 42, no. 18 (April 7, 2011): no. http://dx.doi.org/10.1002/chin.201118241.
Повний текст джерелаDaoust, Benoit, Nicolas Gilbert, Paméla Casault, François Ladouceur, and Simon Ricard. "1,2-Dihaloalkenes in Metal-Catalyzed Reactions." Synthesis 50, no. 16 (July 9, 2018): 3087–113. http://dx.doi.org/10.1055/s-0037-1610174.
Повний текст джерелаMiyabe, Hideto, and Yoshiji Takemoto. "Cascade radical reactions via carbon-carbon/heteroatom bond-forming process." Universal Organic Chemistry 2, no. 1 (2014): 1. http://dx.doi.org/10.7243/2053-7670-2-1.
Повний текст джерелаHosoya, Keisuke, Minami Odagi, and Kazuo Nagasawa. "Guanidine organocatalysis for enantioselective carbon-heteroatom bond-forming reactions." Tetrahedron Letters 59, no. 8 (February 2018): 687–96. http://dx.doi.org/10.1016/j.tetlet.2017.12.058.
Повний текст джерелаCorma, A., A. Leyva-Perez, and Maria J. Sabater. "ChemInform Abstract: Gold-Catalyzed Carbon-Heteroatom Bond-Forming Reactions." ChemInform 42, no. 29 (June 27, 2011): no. http://dx.doi.org/10.1002/chin.201129225.
Повний текст джерелаBanerjee, Bubun. "Microwave-assisted Carbon-carbon and Carbon-heteroatom Bond Forming Reactions - Part 1A." Current Microwave Chemistry 7, no. 1 (June 23, 2020): 3–4. http://dx.doi.org/10.2174/221333560701200422091717.
Повний текст джерелаBanerjee, Bubun. "Microwave-assisted Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions - Part 1B." Current Microwave Chemistry 7, no. 2 (August 6, 2020): 84–85. http://dx.doi.org/10.2174/221333560702200714141435.
Повний текст джерелаBanerjee, Bubun. "Microwave-assisted Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions - Part 2A." Current Microwave Chemistry 8, no. 2 (December 6, 2021): 56–57. http://dx.doi.org/10.2174/221333560802211028163413.
Повний текст джерелаДисертації з теми "Carbon-heteroatom Bond Forming Reactions"
Maluenda, Borderas Irene. "(N-heterocyclic carbene) : metal catalysed carbon-carbon and carbon-heteroatom bond-forming reactions." Thesis, University of Sussex, 2018. http://sro.sussex.ac.uk/id/eprint/76274/.
Повний текст джерелаCazin, Catherine Suzanne Julienne. "Catalysis of carbon-carbon and carbon-heteroatom bond-forming reactions : the importance of the palladium source." Thesis, University of Exeter, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248165.
Повний текст джерелаHoskins, Travis Justin Christopher. "Carbon-carbon bond forming reactions." Thesis, Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/29769.
Повний текст джерелаCommittee Chair: Dr. Christopher Jones; Committee Co-Chair: Dr. Pradeep Agrawal; Committee Member: Dr. Sujit Banerjee; Committee Member: Dr. Tom Fuller. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Casitas, Montero Alícia. "Reactivity of well-defined organometallic copper(III) complexes in carbon-heteroatom bond forming reactions." Doctoral thesis, Universitat de Girona, 2012. http://hdl.handle.net/10803/81985.
Повний текст джерелаAquesta tesi es centra en el camp de la química organometàl•lica del coure(III) que roman sense explorar. Els complexos arilcoure(III) s'han proposat com a intermedis clau en les reaccions de condensació Ullmann que consisteixen en l'acoblament d'halurs d'arils i nucleòfils basats en heteroàtoms catalitzades amb coure. L'estudi de la reactivitat de complexos arilcoure(III) ben definits pot proporcionar una millor comprensió del mecanisme de les reaccions de condensació Ullmann, el qual es troba sota un intens debat. En aquesta tesi doctoral s'estudia la viabilitat del complexos arilcoure(III), estabilitzats en lligands macrocíclics, de participar en reaccions de formació d'enllaç carboni-heteroàtom. S'han desenvolupat reaccions de formació d'enllaç C-N i C-O així com reaccions d'intercanvi d'halurs, on s'inclouen fluoracions, catalitzades amb coure i basades en un cicle catalític Cu(I)/Cu(III) utilitzant substrats models d'halur d'aril. S'ha obtingut una comprensió fonamental de les etapes redox a dos electrons, addició oxidant i eliminació reductiva, en coure.
Graßl, Simon [Verfasser], and Paul [Akademischer Betreuer] Knochel. "Elaboration of electrophilic carbon heteroatom bond forming reactions using organozinc reagents / Simon Graßl ; Betreuer: Paul Knochel." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2020. http://d-nb.info/1210424398/34.
Повний текст джерелаBentz, Emilie Louise Marie. "Zinc enolate coupling : carbon-carbon bond forming reactions." Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.419263.
Повний текст джерелаGates, Bradley Durward. "Novel thermal and electrochemical carbon-carbon bond-forming reactions /." The Ohio State University, 1993. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487847761307998.
Повний текст джерелаMori-Quiroz, Luis Martin. "Transition metal catalyzed Carbon-nitrogen bond forming reactions." Revista de Química, 2015. http://repositorio.pucp.edu.pe/index/handle/123456789/101381.
Повний текст джерелаCarbon-nitrogen (C–N) bond forming reactions are fundamental transformations in nature and also basic processes for the preparation of molecules and materials relevant to human activities. The development of new and efficient reactions for the formation of C–N bonds are therefore of great interest in academic and industrial settings. Progress in the last 20 years has focused mainly in Csp2–N bond forming processes; however, there is growing range of transition metal catalyzed reactions for the introduction of nitrogen in alkyl frameworks (Csp3–N bond formation). This article describes a selection of modern catalytic methods for the formation of C–N bonds.
Tamuang, Suparb. "Mesoporous silica supported catalysts for carbon-carbon bond forming reactions." Thesis, University of Birmingham, 2012. http://etheses.bham.ac.uk//id/eprint/3738/.
Повний текст джерелаMiller, Karen M. (Karen Marie). "Selective, nickel-catalyzed carbon-carbon bond-forming reactions of alkynes." Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/32482.
Повний текст джерелаVita.
Includes bibliographical references.
Catalytic addition reactions to alkynes are among the most useful and efficient methods for preparing diverse types of substituted olefins. Controlling both regioselectivity and (EIZ)- selectivity in such transformations presents a significant challenge. In reactions that also involve the creation of a new stereocenter, the development of enantioselective processes is highly desirable. Several novel, nickel-catalyzed carbon-carbon bond-forming reactions of alkynes that display excellent regioselectivity and (E/Z)-selectivity are described. These reactions afford synthetically useful allylic and homoallylic alcohols, often with high enantioselectivity. A highly enantioselective method for the nickel-catalyzed reductive coupling of alkynes and aldehydes has been realized using the commercially available (+)- neomenthyldiphenylphosphine as a chiral ligand. Allylic alcohols are afforded with complete (E/Z)-selectivity, generally >95:5 regioselectivity, and in up to 96% ee. In conjuction with ozonolysis, this process is complementary to existing methods of enantioselective [alpha]-hydroxy ketone synthesis. In alkene-directed, nickel-catalyzed reductive couplings of 1,3-enynes with aldehydes and epoxides, the conjugated alkene dramatically enhances reactivity and uniformly directs regioselectivity, independent of the nature of the other alkyne substituent (aryl, alkyl (1°, 2°, 3°)) or the degree of alkene substitution (mono-, di-, tri-, and tetrasubstituted). The highly substituted 1,3-diene products are useful in organic synthesis and, in conjunction with a Rh-catalyzed, siteselective hydrogenation, afford allylic and homoallylic alcohols that previously could not be prepared in high regioselectivity (or at all) with related Ni-catalyzed alkyne coupling reactions. Enantiomerically enriched terminal epoxides can be employed to afford enantiomerically enriched homoallylic alcohols. P-chiral, monodentate ferrocenyl phosphine ligands are efficient promoters of catalytic, asymmetric reductive coupling reactions of 1,3-enynes with aromatic aldehydes and with ketones. The latter represents the first catalytic intermolecular reductive coupling of alkynes and ketones, asymmetric or otherwise, to be reported. Both of these methods afford chiral 1,3-dienes in excellent regioselectivity and modest enantioselectivity. Nickel-catalyzed reductive couplings of 1,6-enynes and aldehydes also display very high (>95 : 5) regioselectivity. Use of a monodentate phosphine as an additive leads to formation of the opposite regioisomer in equal and opposite selectivity (5: >95). These results provide strong evidence for an interaction between the remote alkene and the metal center during the regioselectivity-determining step.
by Karen M. Miller..
Ph.D.
Книги з теми "Carbon-heteroatom Bond Forming Reactions"
M, Roberts Stanley, ed. Metal catalysed carbon-carbon bond-forming reactions. Chichester, West Sussex, England: John Wiley, 2004.
Знайти повний текст джерелаRoberts, Stanley M., Jianliang Xiao, John Whittall, and Tom E. Pickett, eds. Catalysts for Fine Chemical Synthesis, Volume 3, Metal Catalysed Carbon-Carbon Bond-Forming Reactions. Chichester, UK: John Wiley & Sons, Ltd, 2004. http://dx.doi.org/10.1002/0470862017.
Повний текст джерелаSharma, Rakesh Kumar, and Bubun Banerjee. Green-Bond Forming Reactions: Carbon-Carbon and Carbon-Heteroatom. de Gruyter GmbH, Walter, 2022.
Знайти повний текст джерелаSharma, Rakesh Kumar, and Bubun Banerjee. Green-Bond Forming Reactions: Carbon-Carbon and Carbon-Heteroatom. de Gruyter GmbH, Walter, 2022.
Знайти повний текст джерелаSharma, Rakesh Kumar, and Bubun Banerjee. Green-Bond Forming Reactions: Carbon-Carbon and Carbon-Heteroatom. de Gruyter GmbH, Walter, 2022.
Знайти повний текст джерелаFagnou, Keith. New rhodium-catalyzed carbon-carbon and carbon-heteroatom bond forming reactions for organic synthesis. 2002.
Знайти повний текст джерелаDanheiser, Rick L. Asymmetric Carbon-Carbon Bond Forming Reactions. Wiley & Sons, Incorporated, John, 2018.
Знайти повний текст джерелаRoberts, Stanley M., John Whittall, Jianliang Xiao, and Tom E. Pickett. Metal Catalysed Carbon-Carbon Bond-Forming Reactions. Wiley & Sons, Incorporated, John, 2007.
Знайти повний текст джерелаRoberts, Stanley M., John Whittall, Jianliang Xiao, and Tom E. Pickett. Catalysts for Fine Chemical Synthesis - Metal Catalysed Carbon-Carbon Bond-Forming Reactions. Wiley & Sons Australia, Limited, John, 2005.
Знайти повний текст джерелаQuach, Tan Dai. Organotrifluoroborate salts in palladium-catalyzed carbon-carbon and copper-mediated carbon-nitrogen bond forming reactions. 2002.
Знайти повний текст джерелаЧастини книг з теми "Carbon-heteroatom Bond Forming Reactions"
Koser, Gerald F. "Heteroatom-Heteroatom-Bond Forming Reactions." In Hypervalent Iodine Chemistry, 173–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_6.
Повний текст джерелаKoser, Gerald F. "C-Heteroatom-Bond Forming Reactions." In Hypervalent Iodine Chemistry, 137–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_5.
Повний текст джерелаAtta-ur-Rahman and Zahir Shah. "Stereoselective Carbon-Carbon Bond Forming Reactions." In Stereoselective Synthesis in Organic Chemistry, 185–396. New York, NY: Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4613-8327-7_4.
Повний текст джерелаParashar, Rakesh Kumar. "Carbon-Carbon Double Bond Forming Reactions." In Reaction Mechanisms in Organic Synthesis, 148–90. West Sussex, United Kingdom: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118681299.ch4.
Повний текст джерелаWolfe, John P., Joshua D. Neukom, and Duy H. Mai. "Synthesis of Saturated Five-Membered Nitrogen Heterocycles via Pd-Catalyzed CN Bond-Forming Reactions." In Catalyzed Carbon-Heteroatom Bond Formation, 1–34. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch1.
Повний текст джерелаMaruoka, Keiji. "Asymmetric Carbon-Carbon Bond-Forming Reactions: Asymmetric Cycloaddition Reactions." In Catalytic Asymmetric Synthesis, 465–91. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471721506.ch14.
Повний текст джерелаMikami, Koichi, and Takeshi Nakai. "Asymmetric Carbon-Carbon Bond-Forming Reactions: Asymmetric Ene Reactions." In Catalytic Asymmetric Synthesis, 543–68. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471721506.ch17.
Повний текст джерелаKanai, Motomu, and Masakatsu Shibasaki. "Asymmetric Carbon-Carbon Bond-Forming Reactions: Asymmetric Michael Reactions." In Catalytic Asymmetric Synthesis, 569–92. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471721506.ch18.
Повний текст джерелаParashar, Rakesh Kumar. "Transition Metal-Mediated Carbon-Carbon Bond Forming Reactions." In Reaction Mechanisms in Organic Synthesis, 191–223. West Sussex, United Kingdom: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118681299.ch5.
Повний текст джерелаTrost, Barry M., and Chulbom Lee. "Asymmetric Carbon-Carbon Bond-Forming Reactions: Asymmetric Allylic Alkylation Reactions." In Catalytic Asymmetric Synthesis, 593–649. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471721506.ch19.
Повний текст джерела