Littérature scientifique sur le sujet « Heteroatom Bond »
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Articles de revues sur le sujet "Heteroatom Bond"
Kotun, Stefan P., et Darryl D. DesMarteau. « Superacid-induced ring-opening reactions of fluorinated heterocycles ». Canadian Journal of Chemistry 67, no 11 (1 novembre 1989) : 1724–28. http://dx.doi.org/10.1139/v89-265.
Texte intégralKadjo, François Kassi, Sopi Thomas Affi, Yao Silvère Diki N’guessan, Mamadou Guy-Richard Koné, Georges Stéphane Dembélé et Nahossé Ziao. « Theoretical Characterization of the Hydrogen Bonding Interaction Sites of Mycolactone C Using the ONIOM Method ». Mediterranean Journal of Chemistry 11, no 2 (26 avril 2021) : 185. http://dx.doi.org/10.13171/mjc02104261574mgrk.
Texte intégralYamamoto, Yuki, Qiqi Chen et Akiya Ogawa. « Diphenyl Diselenide-Assisted Radical Addition Reaction of Diphenyl Disulfide to Unsaturated Bonds upon Photoirradiation ». Molecules 28, no 6 (7 mars 2023) : 2450. http://dx.doi.org/10.3390/molecules28062450.
Texte intégralCorrea, Arkaitz, Olga García Mancheño et Carsten Bolm. « Iron-catalysed carbon–heteroatom and heteroatom–heteroatom bond forming processes ». Chemical Society Reviews 37, no 6 (2008) : 1108. http://dx.doi.org/10.1039/b801794h.
Texte intégralZou, Song, Sheng Wang et Chanjuan Xi. « ROTf-induced annulation of heteroatom reagents and unsaturated substrates leading to cyclic compounds ». Royal Society Open Science 5, no 11 (novembre 2018) : 181389. http://dx.doi.org/10.1098/rsos.181389.
Texte intégralSkalik, Joanna, Marek Koprowski, Ewa Różycka-Sokołowska et Piotr Bałczewski. « The hetero-Friedel-Crafts-Bradsher Cyclizations with Formation of Ring Carbon-Heteroatom (P, S) Bonds, Leading to Organic Functional Materials ». Materials 13, no 21 (23 octobre 2020) : 4751. http://dx.doi.org/10.3390/ma13214751.
Texte intégralWaldman, Abraham J., Tai L. Ng, Peng Wang et Emily P. Balskus. « Heteroatom–Heteroatom Bond Formation in Natural Product Biosynthesis ». Chemical Reviews 117, no 8 (4 avril 2017) : 5784–863. http://dx.doi.org/10.1021/acs.chemrev.6b00621.
Texte intégralZybill, Christian. « The silicon heteroatom bond ». Inorganica Chimica Acta 202, no 1 (décembre 1992) : 119–20. http://dx.doi.org/10.1016/s0020-1693(00)85362-1.
Texte intégralEaborn, Colin. « The silicon-heteroatom bond ». Journal of Organometallic Chemistry 427, no 3 (avril 1992) : C41. http://dx.doi.org/10.1016/0022-328x(92)80084-b.
Texte intégralCai, Xiao-Hua, Meng-Zhi Yang et Bing Xie. « Recent Investigations on the Functionalizations of C(sp3)-H Bonds Adjacent to a Heteroatom ». Letters in Organic Chemistry 16, no 10 (23 août 2019) : 779–801. http://dx.doi.org/10.2174/1570178616666190123131353.
Texte intégralThèses sur le sujet "Heteroatom Bond"
Zárate, Sáez Cayetana. « C-heteroatom bond-formation via ni-catalyzed c-o bond cleavage ». Doctoral thesis, Universitat Rovira i Virgili, 2017. http://hdl.handle.net/10803/401555.
Texte intégralA pesar de que el campo del acoplamiento cruzado ha desarrollado increíbles avances, la gran mayoría de procesos todavía se basa en el uso de halogenuros de arilo. Sin embargo, este tipo de electrófilos presentan una toxicidad intrínseca y, a su vez, su síntesis resulta tediosa, especialmente cuando se trata de halogenuros de arilo altamente funcionalizados. Debido a ello, la comunidad sintética se ha volcado en la búsqueda de alternativas al uso de halogenuros de arilo en química de acoplamiento cruzado. Un gran esfuerzo se ha desarrollado en la última década para implementar los derivados del fenol en este tipo de transformacions debido a la abundancia natural y comercial de dichos compuestos y a su baja toxicidad en comparación con los organohalogenuros. Sin embargo, la alta energía de activación necesaría para romper los enlaces C-O ha limitado considerablemenete el uso de derivados del fenol en reacciones de acomplamineto cruzado, sobre todo si se trata de éteres de metilo. Actualmente la gran mayoría de métodos basados en esta familia de electrófilos se utilizan en la formación de enlaces C-C. De lo contrario, apenas existen técnicas para obtener enlaces C-heteroátomo probablemente debido a la baja reactividad de los nucleófilos donde la densidad de carga negativa reside en un heteroátomo. La presente tesis docotoral se ha centrado en el desarrollo de nuevas metodologías para la creación de enlaces de tipo C-heteroatomo mediante la activción catalítica de enlaces C-O con complejos de Ni. Se han descrito novedosos métodos de sililación y borilación de ésteres y metil éteres de arilo y bencilo. Dichos métodos suponen una via alternativa para la síntesis de silanos y boronatos, los cuales son intermedios de gran utilidad en síntesis orgánica. Además, el descubrimiento de unas condiciones totalmente inusuales para activar enlaces de tipo C-OMe ha abierto nuevas perspectivas sobre la reactividad de este tipo de enlaces y, a la vez, ha sugerido la existencia de nuevos mecanismos de activación.
While the field of cross-coupling has reached remarkable levels of sophistication, the vast majority of processes are still being conducted with organic halide counterparts. Drawbacks associated to their toxicity and the limited accessibility of densely functionalized aryl halides have prompted chemists to develop powerful, yet practical, alternatives. Among these, the utilization of phenol derivatives as coupling partners via C-O bond cleavage would be particularly rewarding due to their readily availability and benign nature. However, the high activation energy required for effecting C–O bond cleavage has become a daunting challenge when devising catalytic techniques using phenol derivatives, specially always-elusive aryl methyl ethers. At present, the vast majority of cross-coupling reactions using phenol derivatives remains confined to C–C bond formation, whereas the formation of C-heteroatom bonds has been poorly studied, likely due to the less reactivity of heteroatom-based nucleophiles. This doctoral thesis has focused on the development of new methodologies for forging C-heteroatom bonds via Ni-catalyzed C-O bond cleavage. It has been described new protocols for the silylation and borylation of aryl and benzyl esters and methyl ethers. These methodologies can be used as useful alternatives towards the synthesis of aryl and benzyl silanes and boronates, incredible important intermediates in organic synthesis. Furthermore, the discovery of unusual, yet surprising, conditions for the cleavage of C-OMe bonds have opened up new vistas towards the reactivity of aryl and benzyl methyls ethers while suggesting new activation pathways.
van, Rooy Sara Emily. « Reactivity of rhodium-heteroatom bonds : from catalytic bond activation to new strategies for olefin functionalization ». Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/444.
Texte intégralNiljianskul, Nootaree. « New Pd and Cu-based catalysts for carbon-heteroatom bond formation ». Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/98784.
Texte intégralCataloged from PDF version of thesis.
Includes bibliographical references.
The research presented in this dissertation is aimed at the development of novel methodologies for carbon-heteroatom cross-coupling reactions catalyzed by late-transition metals. Both palladium and copper are central to the field of transition metal-catalysis and are integral to the catalyst systems developed as part of our continual advancement in cross-coupling reactions. The first part of this thesis focuses on the use of palladium catalysts to form carbon-sulfur bonds directed towards aryl sulfonamide synthesis. The second part of the thesis describes the recent development in the copper(!) hydride mediated formation of carbon-nitrogen bonds via hydroamination of olefins. Part I. Chapter 1. Palladium-Catalyzed Chlorosulfonylation of Arylboronic Acids Using a biaryl phosphine ligand platform, the first palladium-catalyzed cross-coupling reaction of phenyl chlorosulfate with arylboronic acids was achieved. In this context, the arylsulfonyl chloride products serve as useful precursors to a variety of sulfonyl functional groups, such as aryl sulfonamides, aryl sulfones, and arenesulfonate esters. In particular, this method allows for the preparation of a number of arylsulfonyl chlorides that are not accessible via electrophilic aromatic substitution pathways and under mild reaction conditions. Additionally, this methodology points to an unprecedented selectivity for the phenylchlorosulfate electrophiles used in the cross-coupling reactions. Part II. Chapter 2. Enantio- and Regioselective Copper-Catalyzed Hydroamination of Styrenes and the Extension of the Methodology towards Anti-Markovnikov Hydroamination of Terminal Aliphatic Alkenes The development of a copper-mediated strategy towards the hydroamination of styrene derivatives is reported. In this system, the reaction proceeds regioselectively and enantioselectively to generate [alpha]-branched amines. The system can transform a wide variety of substituted styrenes, including trans-, cis-, and [beta]-disubstituted styrenes. In addition, our extension to copper-catalyzed hydroamination reactions of unactivated aliphatic olefins is reported. Using terminal aliphatic alkenes, the copper-catalyzed hydroamination reactions proceed with anti-Markovnikov regioselectivity. Preliminary results point to the application of this methodology towards [beta]-chiral amine synthesis via the hydroamination of I, 1-disubstituted alkenes. Chapter 3. [alpha]-Aminosilane Synthesis via Copper-Catalyzed Hydroamination of Vinylsilanes The copper-catalyzed hydroamination of vinylsilanes is described. This regioselective reaction generates a-chiral aminosilanes in high yields and enantioselectivities. The method is compatible with differentially substituted vinylsilanes and allows access to many valuable chiral organosilicon compounds. Chapter 4. Synthesis of [gamma]-Chiral Amines via Copper-Catalyzed Hydroamination of 3,3- Disubstituted Allylic Alcohols and 3,3-Disubstituted Allylic Benzoates An investigation into the copper-catalyzed hydroamination of allylic alcohols and allylic benzoates is reported. The reaction proceeds via a [beta]-alkoxy elimination, setting a stereogenic center at the 3-postion to generate [gamma]-chiral amine products. The reaction is more efficient using allylic benzoates. This method is completely regioselective and is applicable to aliphatic allylic benzoates as well as aromatic allylic benzoates. Additionally, we demonstrated that this strategy is applicable towards an allylic epoxide substrate to generate [delta]-chiral amine.
by Nootaree Niljianskul.
Ph. D. in Organic Chemistry
Ly, Tuan Q. « New heteroatom ligands and metalla-heterocycles via P-N bond formation ». Thesis, Loughborough University, 1997. https://dspace.lboro.ac.uk/2134/32271.
Texte intégralOliver, Thomas Albert Anthony. « Exploring photoinduced heteroatom-H bond fission in the gas and solution phases ». Thesis, University of Bristol, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541647.
Texte intégralDe, Fusco Claudia. « Stereoselective carbon-carbon and carbon-heteroatom bond formation mediated by bifunctional organocatalysts ». Doctoral thesis, Universita degli studi di Salerno, 2013. http://hdl.handle.net/10556/1323.
Texte intégralThis PhD work describes the development of different Michael and Michael type processes employing different bifunctional organocatalysts. All the processes studied involved a non-covalent activation of the substrates provided by the organic promoters. An asymmetric epoxidation of electron-poor trisubstituted olefins has been developed by employing the commercially available diphenyl prolinol which afforded the epoxides in high yield, complete diastereocontrol and good enantioselectivity. Diaryl prolinols were found to promote a Michael addition of -ketoesters to nitroalkenes. An unexpected high efficiency and stereocontrol was observed with hexafluorobenzene as unconventional solvent, but also employed as an additive. A convenient tandem double Michael addition process was developed to access symmetrically and unsymmetrically 3,5-diaryl substituted cyclohexanones by using quinine as catalyst. An aziridination reaction of terminal electron-poor olefins has been disclosed by using a commercially available aminothiourea catalyst. The desired aziridines, bearing a quaternary stereocenter, were isolated in good yield and enantiocontrol. These compounds, were regioselectively ring-opened to access valuable ,-disubstituted -amino ester derivatives. Finally an asymmetric Fischer indolization to produce helical molecules was investigated employing a chiral phosphoric acid as promoter and an ion-exchange polymer as ammonia scavenger. [edited by author]
XI n.s.
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/.
Texte intégralTsang, Melanie Wing-Sze. « Pd-catalysed carbon-heteroatom bond formation and urea synthesis in supercritical carbon dioxide ». Thesis, University of Cambridge, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.614105.
Texte intégralCasitas, 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.
Texte intégralAquesta 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.
Reding, Matthew Todd. « The development and synthetic application of titanium-mediated carbon-heteroatom double bond hydrosilylation methodologies ». Thesis, Massachusetts Institute of Technology, 1997. http://hdl.handle.net/1721.1/42643.
Texte intégralLivres sur le sujet "Heteroatom Bond"
A, Armitage D., Patai Saul et Rappoport Zvi, dir. The Silicon-heteroatom bond. Chichester, West Sussex, England : Wiley, 1991.
Trouver le texte intégralYudin, Andrei K., dir. Catalyzed Carbon-Heteroatom Bond Formation. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.
Texte intégralArmitage, D. A. (Fred), Robert J. P. Corriu, Tom C. Kendrick, Bhukan Parbhoo, T. Don Tilley, James W. White et J. Colin Young, dir. The Silicon-Heteroatom Bond (1991). Chichester, UK : John Wiley & Sons, Inc., 1991. http://dx.doi.org/10.1002/9780470772447.
Texte intégralCatalyzed carbon-heteroatom bond formation. Weinheim, Germany : Wiley-VCH, 2011.
Trouver le texte intégralJones, Keith. Carbon with one heteroatom attached by a multiple bond. Amsterdam [etc] : Elsevier, 2005.
Trouver le texte intégralWolfe, John P., dir. Synthesis of Heterocycles via Metal-Catalyzed Reactions that Generate One or More Carbon-Heteroatom Bonds. Berlin, Heidelberg : Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-38880-4.
Texte intégralArmitage, D. A., Robert Corriu, Tom C. Kendrick, Bhukan Parbhoo et T. Don Tilley. Silicon-Heteroatom Bond. Wiley & Sons, Limited, John, 2010.
Trouver le texte intégralYudin, Andrei K., et John F. Hartwig. Catalyzed Carbon-Heteroatom Bond Formation. Wiley & Sons, Limited, John, 2010.
Trouver le texte intégralYudin, Andrei K., et John F. Hartwig. Catalyzed Carbon-Heteroatom Bond Formation. Wiley & Sons, Incorporated, John, 2011.
Trouver le texte intégralYudin, Andrei K., et John F. Hartwig. Catalyzed Carbon-Heteroatom Bond Formation. Wiley & Sons, Incorporated, John, 2010.
Trouver le texte intégralChapitres de livres sur le sujet "Heteroatom Bond"
Koser, Gerald F. « Heteroatom-Heteroatom-Bond Forming Reactions ». Dans Hypervalent Iodine Chemistry, 173–83. Berlin, Heidelberg : Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_6.
Texte intégralAtta-ur-Rahman et Zahir Shah. « Asymmetric Carbon-Heteroatom Bond Formations ». Dans Stereoselective Synthesis in Organic Chemistry, 416–33. New York, NY : Springer New York, 1993. http://dx.doi.org/10.1007/978-1-4613-8327-7_6.
Texte intégralKoser, Gerald F. « C-Heteroatom-Bond Forming Reactions ». Dans Hypervalent Iodine Chemistry, 137–72. Berlin, Heidelberg : Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-46114-0_5.
Texte intégralFleming, Matthew J., et Mark Lautens. « CarbonHeteroatom Bond Formation by RhI-Catalyzed Ring-Opening Reactions ». Dans Catalyzed Carbon-Heteroatom Bond Formation, 411–36. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch10.
Texte intégralWolfe, John P., Joshua D. Neukom et Duy H. Mai. « Synthesis of Saturated Five-Membered Nitrogen Heterocycles via Pd-Catalyzed CN Bond-Forming Reactions ». Dans Catalyzed Carbon-Heteroatom Bond Formation, 1–34. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch1.
Texte intégralWidenhoefer, Ross A., et Feijie Song. « Gold-Catalyzed Addition of Nitrogen and Sulfur Nucleophiles to CC Multiple Bonds ». Dans Catalyzed Carbon-Heteroatom Bond Formation, 437–61. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch11.
Texte intégralWidenhoefer, Ross A., et Feijie Song. « Gold-Catalyzed Addition of Oxygen Nucleophiles to CC Multiple Bonds ». Dans Catalyzed Carbon-Heteroatom Bond Formation, 463–92. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch12.
Texte intégralYeung, Charles S., Peter K. Dornan et Vy M. Dong. « Transition Metal Catalyzed Approaches to Lactones Involving CO Bond Formation ». Dans Catalyzed Carbon-Heteroatom Bond Formation, 35–68. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch2.
Texte intégralBeletskaya, Irina P., et Valentine P. Ananikov. « The Formation of Csp2S and Csp2Se Bonds by Substitution and Addition Reactions Catalyzed by Transition Metal Complexes ». Dans Catalyzed Carbon-Heteroatom Bond Formation, 69–118. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch3.
Texte intégralJacques, Béatrice, et Kilian Muñiz. « Palladium Catalysis for Oxidative 1,2-Difunctionalization of Alkenes ». Dans Catalyzed Carbon-Heteroatom Bond Formation, 119–35. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633388.ch4.
Texte intégralActes de conférences sur le sujet "Heteroatom Bond"
Alexey, Sukhorukov, Pavel Ushakov, Yana Naumovich et Sema Ioffea. « NEW METHODS FOR THE CONSTRUCTION OF CARBON-CARBON AND CARBON-HETEROATOM BONDS UTILIZING NITRO-DERIVATIVES ». Dans Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m721.aks-2019/53-55.
Texte intégralRapports d'organisations sur le sujet "Heteroatom Bond"
Hartwig, John. Chemistry of Complexes with Transition Metal Heteroatom Bonds Novel Insertion Chemistry and XH Bond Activation. Office of Scientific and Technical Information (OSTI), février 2012. http://dx.doi.org/10.2172/1035516.
Texte intégralKlein, D. The synthesis and reactivity of organoiridium complexes containing metal-heteroatom bonds. Office of Scientific and Technical Information (OSTI), novembre 1989. http://dx.doi.org/10.2172/7249432.
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