Relevant bibliographies by topics / Electrophilic amination

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

Academic literature on the topic 'Electrophilic amination'

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

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Journal articles on the topic "Electrophilic amination"

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Bandara, H. M. D., D. Jin, M. A. Mantell, et al. "Non-directed aromatic C–H amination: catalytic and mechanistic studies enabled by Pd catalyst and reagent design." Catalysis Science & Technology 6, no. 14 (2016): 5304–10. http://dx.doi.org/10.1039/c6cy00457a.

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Zhou, Zhe, and László Kürti. "Electrophilic Amination: An Update." Synlett 30, no. 13 (2019): 1525–35. http://dx.doi.org/10.1055/s-0037-1611861.

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In this account, we provide an overview of some recent advances in electrophilic amination methodologies that have been developed in the Kürti group over the last seven years. Our group’s focus has been to develop novel amination methodologies that directly yield N-unprotected amine products.1 Introduction2 Amination of Boronic Acids3 Aziridination of Unactivated Olefins4 Rhodium-Catalyzed C–H Amination of Arenes5 Synthesis of Carbazoles6 Amination of Aryl- and Alkylmetals7 Doubly Electrophilic N-Linchpin Reagents8 Aza-Rubottom Oxidation of Silyl Enol Ethers9 Summary
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Erdik, Ender, and Mehmet Ay. "Electrophilic amination of carbanions." Chemical Reviews 89, no. 8 (1989): 1947–80. http://dx.doi.org/10.1021/cr00098a014.

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Niwa, Yasuki, Kazuki Takayama, and Makoto Shimizu. "Electrophilic amination with iminomalonate." Tetrahedron Letters 42, no. 32 (2001): 5473–76. http://dx.doi.org/10.1016/s0040-4039(01)01022-x.

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Rauser, Marian, Christoph Ascheberg, and Meike Niggemann. "Electrophilic Amination with Nitroarenes." Angewandte Chemie International Edition 56, no. 38 (2017): 11570–74. http://dx.doi.org/10.1002/anie.201705356.

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Rauser, Marian, Christoph Ascheberg, and Meike Niggemann. "Electrophilic Amination with Nitroarenes." Angewandte Chemie 129, no. 38 (2017): 11728–32. http://dx.doi.org/10.1002/ange.201705356.

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Velarde-Ortiz, Raffet, Albert Guijarro, and Reuben D. Rieke. "Electrophilic amination of organozinc halides." Tetrahedron Letters 39, no. 50 (1998): 9157–60. http://dx.doi.org/10.1016/s0040-4039(98)02108-x.

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Greck, Christine, and Jean Genêt. "Electrophilic Amination: New Synthetic Applications." Synlett 1997, no. 7 (1997): 741–48. http://dx.doi.org/10.1055/s-1997-5745.

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Gouverneur, V., and L. Ghosez. "Electrophilic amination of 2-azadienes." Tetrahedron 52, no. 21 (1996): 7585–98. http://dx.doi.org/10.1016/0040-4020(96)00268-2.

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Fukami, Yutaro, Takamasa Wada, Tatsuhiko Meguro, Noritaka Chida, and Takaaki Sato. "Copper-catalyzed electrophilic amination using N-methoxyamines." Organic & Biomolecular Chemistry 14, no. 24 (2016): 5486–89. http://dx.doi.org/10.1039/c5ob02167g.

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Dissertations / Theses on the topic "Electrophilic amination"

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Berman, Ashley M. Johnson Jeffrey Scott. "Catalytic electrophilic amination reactions." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2007. http://dc.lib.unc.edu/u?/etd,1086.

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Thesis (Ph. D.)--University of North Carolina at Chapel Hill, 2007.<br>Title from electronic title page (viewed Mar. 27, 2008). "... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry." Discipline: Chemistry; Department/School: Chemistry.
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Edmonds, Ian David. "Novel oxaziridines for asymmetric electrophilic amination." Thesis, Imperial College London, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415010.

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Filip, Sorin V. "Studies towards the stereoselective electrophilic amination of carbanions." [S.l. : s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=966042026.

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Bordogna, Celine. "New reagents for electrophilic amination and asymmetric aziridination." Thesis, University of East Anglia, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.522283.

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Murrell, Victor Leon. "New systems for asymmetric electrophilic heteroatom transfer." Thesis, Loughborough University, 1999. https://dspace.lboro.ac.uk/2134/27068.

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Arnall-Culliford, Jennifer Charlotte. "Planar chiral ferrocene lithium amide bases : a new generation of bases for asymmetric synthesis." Thesis, University of Nottingham, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.251971.

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Bedier, Matthieu. "Synthèse et Réactivité des Fluorures Allyliques Fonctionnalisés (alpha-Fluoroénamides) et Applications Synthétiques." Thesis, Normandie, 2018. http://www.theses.fr/2018NORMR033/document.

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Le fluor a gagné un intérêt croissant dans de nombreux domaines de la chimie organique. De nombreuses méthodes de fluoration ont vu le jour afin de répondre à une demande croissante en molécules fluorées les plus diverses. Cependant certains synthons restent difficiles à obtenir par des moyens efficaces. Une réaction de fluoration électrophile d’allylsilanes a été développé afin d’accéder à des motifs α-fluroénamides hautement fonctionnalisés. Ces α-fluroénamides peuvent être de types variés : benzylamines, anilines, ou alkyles… Un accent particulier a été mis sur des dérivés d’acides aminés p
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Eichman, Chad. "Development of Electrophilic Amination with Oximes for the Synthesis of Nitrogen-Containing Heterocycles; Transition Metal Catalysts for Carbon-Sulfur and Carbon-Carbon Bond Formation and Selective C-H Activation." The Ohio State University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=osu1275430570.

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Campbell, Matthew James Johnson Jeffrey Scott. "I. Mechanistic studies of a copper-catalyzed electrophilic amination of diorganozinc reagents reagents by O-benzoyl N,N-dialkylhydroxylamines II. Development of a 3-Exo-Dig cyclization for the preparation of vinylidene cyclopropanes III. Total synthesis of +-polyanthellin A." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2009. http://dc.lib.unc.edu/u?/etd,2881.

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Thesis (Ph. D.)--University of North Carolina at Chapel Hill, 2010.<br>Title from electronic title page (viewed Jun. 23, 2010). "... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry." Discipline: Chemistry; Department/School: Chemistry.
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Walker, Whitney Kaye. "Electrophilic Catalysis Using Heterobimetallic Complexes." BYU ScholarsArchive, 2017. https://scholarsarchive.byu.edu/etd/6962.

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Conventional ligand design in transition metal catalysis capitalizes on the ability of phosphorous, nitrogen, carbon, oxygen, and sulfur-based donors to modify the steric and electronic properties of a reactive metal center. Heterobimetallic transition metal complexes that contain a dative metal-metal bond provide a unique approach to ligand design where the reactivity of the metal center can be modified by metal-metal electronic communication. Our laboratory is interested in using the unique properties of heterobimetallic complexes to address significant limitations in current transition meta
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Books on the topic "Electrophilic amination"

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McDonald, Stacey L. Copper-Catalyzed Electrophilic Amination of sp2 and sp3 C−H Bonds. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-38878-6.

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McDonald, Stacey L. Copper-Catalyzed Electrophilic Amination of sp2 and sp3 C-H Bonds. Springer, 2016.

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McDonald, Stacey L. Copper-Catalyzed Electrophilic Amination of sp2 and sp3 C−H Bonds. Springer, 2018.

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4

Denmark, Scott E., Kevin H. Shaughnessy, Engelbert Ciganek, and Rebecca B. DeVasher. Copper-Catalyzed Amination of Aryl and Alkenyl Electrophiles. Wiley & Sons, Incorporated, John, 2017.

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Denmark, Scott E., Kevin H. Shaughnessy, Engelbert Ciganek, and Rebecca B. DeVasher. Copper-Catalyzed Amination of Aryl and Alkenyl Electrophiles. Wiley & Sons, Incorporated, John, 2017.

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Book chapters on the topic "Electrophilic amination"

1

McDonald, Stacey L. "Electrophilic Amination for the Synthesis of Alkyl and Aryl Amines." In Springer Theses. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-38878-6_1.

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McDonald, Stacey L. "Copper-Catalyzed Electrophilic Amination of Heteroarenes and Arenes by C–H Zincation." In Springer Theses. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-38878-6_4.

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3

Dembech, Pasquale, Alfredo Ricci, and Giancarlo Seconi. "New Trends in Electrophilic Amination: From Simple Achiral and Chiral Amines and Hydrazines to Advanced Materials." In Current Trends in Organic Synthesis. Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4801-0_13.

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Blakemore, P. R. "Electrophilic Amination of Amides." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00907.

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Witulski, B., and C. Alayrac. "Electrophilic Amination of Metal Acetylides." In Three Carbon-Heteroatom Bonds: Ketenes and Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-01012.

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6

Wolkenberg, S. E., and R. M. Garbaccio. "Electrophilic Amination of Chiral Enolates Using Azodicarboxylates." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00369.

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Wolkenberg, S. E., and R. M. Garbaccio. "Electrophilic Amination of Chiral Enolates Using Sulfonyl Azides." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00372.

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Wolkenberg, S. E., and R. M. Garbaccio. "Electrophilic Amination of Chiral Silyl Enol Ethers with Azodicarboxylates." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00370.

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Wolkenberg, S. E., and R. M. Garbaccio. "Electrophilic Amination of Enolates Using 1-Chloro-1-nitrosocyclohexane." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00374.

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"7.1. Formation of C—N Bonds by Electrophilic Amination." In Stereoselective Synthesis, edited by Günter Helmchen, Reinhard W. Hoffmann, Johann Mulzer, and Ernst Schaumann. Georg Thieme Verlag, 1995. http://dx.doi.org/10.1055/b-0035-115224.

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