Literatura académica sobre el tema "Imines"
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Artículos de revistas sobre el tema "Imines"
Svete, Jurij, Uroš Grošelj, Franc Požgan y Bogdan Štefane. "Copper-Catalyzed Azomethine Imine–Alkyne Cycloadditions (CuAIAC)". Synthesis 50, n.º 23 (5 de octubre de 2018): 4501–24. http://dx.doi.org/10.1055/s-0037-1610284.
Texto completoWulff, William, Xin Zhang y Yijing Dai. "The Acceleration of the Rearrangement of α-Hydroxy Aldimines by Lewis or Brønsted Acids". Synlett 29, n.º 15 (28 de agosto de 2018): 2015–18. http://dx.doi.org/10.1055/s-0037-1610262.
Texto completoGonciarz, Agnieszka, Robert Pich, Krzysztof Artur Bogdanowicz, Beata Jewloszewicz, Wojciech Przybył, Karolina Dysz, Agnieszka Dylong et al. "UV–Vis Absorption Properties of New Aromatic Imines and Their Compositions with Poly({4,8-bis[(2-Ethylhexyl)oxy]Benzo[1,2-b:4,5-b′]Dithiophene-2,6-diyl}{3-Fluoro-2-[(2-Ethylhexyl)Carbonyl]Thieno[3,4-b]Thiophenediyl})". Materials 12, n.º 24 (13 de diciembre de 2019): 4191. http://dx.doi.org/10.3390/ma12244191.
Texto completoMendes, Joseane A., Paulo R. R. Costa, Miguel Yus, Francisco Foubelo y Camilla D. Buarque. "N-tert-Butanesulfinyl imines in the asymmetric synthesis of nitrogen-containing heterocycles". Beilstein Journal of Organic Chemistry 17 (12 de mayo de 2021): 1096–140. http://dx.doi.org/10.3762/bjoc.17.86.
Texto completoGarrido-Castro, Alberto F., M. Carmen Maestro y José Alemán. "α-Functionalization of Imines via Visible Light Photoredox Catalysis". Catalysts 10, n.º 5 (19 de mayo de 2020): 562. http://dx.doi.org/10.3390/catal10050562.
Texto completoNugent, Thomas C., Richard Vaughan Williams, Andrei Dragan, Alejandro Alvarado Méndez y Andrei V. Iosub. "An investigation of the observed, but counter-intuitive, stereoselectivity noted during chiral amine synthesis via N-chiral-ketimines". Beilstein Journal of Organic Chemistry 9 (15 de octubre de 2013): 2103–12. http://dx.doi.org/10.3762/bjoc.9.247.
Texto completoRawaa Daoud Sulaiman y Zaheda Ahmed Najim. "The Effect of Temperature and Thermodynamic Parameters on the Ionization Constants of Some Imines Derived from Vanillin with substituted aniline". Tikrit Journal of Pure Science 27, n.º 4 (28 de noviembre de 2022): 31–38. http://dx.doi.org/10.25130/tjps.v27i4.30.
Texto completoAn, Ran, Mengbi Guo, Yingbo Zang, Hang Xu, Zhuang Hou y Chun Guo. "Recent Advances in Synthesis of Benzazoles via Imines". Current Organic Chemistry 24, n.º 17 (12 de noviembre de 2020): 1897–942. http://dx.doi.org/10.2174/1385272824999200818180845.
Texto completoFreese, Tyll, Jan C. Namyslo, Martin Nieger y Andreas Schmidt. "Sulfur, mercury, and boron adducts of sydnone imine derived anionic N-heterocyclic carbenes". RSC Advances 9, n.º 9 (2019): 4781–88. http://dx.doi.org/10.1039/c9ra00294d.
Texto completoZhang, Hanmo, E. Ben Hay, Stephen J. Geib y Dennis P. Curran. "Fates of imine intermediates in radical cyclizations of N-sulfonylindoles and ene-sulfonamides". Beilstein Journal of Organic Chemistry 11 (17 de septiembre de 2015): 1649–55. http://dx.doi.org/10.3762/bjoc.11.181.
Texto completoTesis sobre el tema "Imines"
Lavergne, Kaitlyn. "Synthesis of Azomethine Imines via Alkene Aminocarbonylation and their Derivatization into Pyrazolones". Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32516.
Texto completoYoung, Adrian R. "Free radical cyclisation of imines". Thesis, Loughborough University, 1996. https://dspace.lboro.ac.uk/2134/15357.
Texto completoTillman, Anna Louise. "Organocatalytic, enantioselective additions to imines". Thesis, University of Cambridge, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612994.
Texto completoHeaney, Mary Frances Teresa. "Cycloaddition reactions of oximes and imines". Thesis, Queen's University Belfast, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.335415.
Texto completoBlack, 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.
Kovaricek, Petr. "Motional, reactional and constitutional dynamics of imines". Phd thesis, Université de Strasbourg, 2014. http://tel.archives-ouvertes.fr/tel-01059611.
Texto completoHartley, James Holroyd. "Saccharide accelerated hydrolysis of boronic acid imines". Thesis, University of Birmingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.369335.
Texto completoRajamäki, Suvi Henna Maria. "Lewis acid mediated cyclisations of methylenecyclopropyl imines". Thesis, University of Southampton, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.401829.
Texto completoGuillemin, Jean-Claude. "Les imines non-stabilisees : synthese et reactivite". Rennes 1, 1986. http://www.theses.fr/1986REN10053.
Texto completoGuillemin, Jean-Claude. "Les Imines non-stabilisées synthèse et réactivité". Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37598084v.
Texto completoLibros sobre el tema "Imines"
Johnson, A. William. Ylides and imines of phosphorus. New York: Wiley, 1993.
Buscar texto completoKimpe, Norbert De. The chemistry of &-haloketones, &-haloaldehydes and &-haloimines. Chichester, England: Wiley, 1988.
Buscar texto completoHartley, James Holroyd. Saccharide accelerated hydrolysis of boronic acid imines. Birmingham: University of Birmingham, 2000.
Buscar texto completoKimpe, Norbert de. The chemistry of [alpha]-haloketones, [alpha]-haloaldehydes, and [alpha]-haloimines. Chichester: Wiley, 1988.
Buscar texto completoHallett, David James. Ally lstannanes: Reaction with imines, iminium ions and ketones. Manchester: University of Manchester, 1993.
Buscar texto completoRahid, H. S. New syntheses of imines and chiral B-aminophosphine derivatives. Manchester: UMIST, 1997.
Buscar texto completoPower, Nicholas Patrick. Kinetics and mechanisms of reactions of N-Arylsulfonyl derivatives of imines. [S.l: The Author], 1998.
Buscar texto completoCenter, Langley Research, ed. Modified phenylethynyl containing imides for secondary bonding: Non-autoclave, low twmperature processable adhesives. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1999.
Buscar texto completoMazurkiewicz, Roman. Studium reakcji imidoilowania amidów. Gliwice: Politechnika Śląska, 1989.
Buscar texto completoCenter, Langley Research y United States. National Aeronautics and Space Administration., eds. Synthesis and characterization of modified phenylethynyl terminated polyimides. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1998.
Buscar texto completoCapítulos de libros sobre el tema "Imines"
Rowlands, C. C. y R. D. Farley. "15.7.2 Imines and imides". En Landolt-Börnstein - Group II Molecules and Radicals, 446–54. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-45824-1_56.
Texto completoDilworth, J. R. y S. Morton. "From Imines". En Inorganic Reactions and Methods, 41–43. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch25.
Texto completoOjima, I. "Of Imines". En Inorganic Reactions and Methods, 255–57. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145319.ch83.
Texto completoLi, Wei y Xumu Zhang. "Asymmetric Hydrogenation of Imines". En Stereoselective Formation of Amines, 103–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/128_2013_483.
Texto completoMartin, Dean F. y Edward J. Olszewski. "Metal Derivatives of β-Keto Imines (β-Imino Ketones)". En Inorganic Syntheses, 45–52. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132395.ch14.
Texto completoSharp, John T. "Nitrile Ylides and Nitrile Imines". En Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products, 473–537. New York, USA: John Wiley & Sons, Inc., 2003. http://dx.doi.org/10.1002/0471221902.ch7.
Texto completoVilariño, Natalia, Sara F. Ferreiro, Andrés Crespo y José Gil. "Pharmacology of the cyclic imines". En Phycotoxins, 343–60. Chichester, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118500354.ch15.
Texto completoBailey, Patrick D. y Keith M. Morgan. "Enamines". En Organonitrogen Chemistry. Oxford University Press, 2022. http://dx.doi.org/10.1093/hesc/9780198557753.003.0008.
Texto completoSandler, Stanley R. y Wolf Karo. "IMINES". En Sourcebook of Advanced Organic Laboratory Preparations, 234–36. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-08-092553-0.50035-2.
Texto completoSandler, Stanley R. y Wolf Karo. "IMINES". En Organic Functional Group Preparations, 291–322. Elsevier, 1986. http://dx.doi.org/10.1016/b978-0-08-092557-8.50016-1.
Texto completoActas de conferencias sobre el tema "Imines"
Mas-Marzá, Elena, Ramón Arcas-Martínez, Laxman Gouda y Francisco Fabregat-Santiago. "Photoelectrosynthesis of Imines". En nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.ngfm.2019.271.
Texto completoMas-Marzá, Elena, Ramón Arcas-Martínez, Laxman Gouda y Francisco Fabregat-Santiago. "Photoelectrosynthesis of Imines". En nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.nfm.2019.271.
Texto completoPinho e Melo, Teresa, Ana Cabral y António d'A Rocha Gonsalves. "Intramolecular Cycloaddition of Imines of Cysteine Derivatives". En The 1st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02044.
Texto completoMargulï¾s, L., J. C. Guillemin, Brett McGuire, Anthony Remijan, Olga Dorovskaya, V. Ilyushin y R. Motiyenko. "SUBMILLIMETER WAVE SPECTROSCOPY FOR ISM: IMINES WITH INTERNAL ROTATION". En 74th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.tg05.
Texto completoDiz-Gil, Raquel, Sara Bermúdez-Fernández, Paula Munín-Cruz, María Pereira y José Vila. "Preparation and crystal structure of metallated 2,4,6-trimethylaniline imines". En The 24th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08322.
Texto completoShutalev, Anatoly. "A New Approach to the Synthesis of Hydrogenated Pyrimidine-2-imines". En The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01854.
Texto completoRaposo, M. Manuela y M. Cidália Castro. "Synthesis and Characterization of the Photophysical Properties of Novel Heterocyclic Imines". En The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a048.
Texto completoMOHSIN, Doaa Hadi y Zahraa Hameed KAMIL. "SYNTHESIS AND CHARACTERIZATION OF SOME NEW 1,3-OXAZEPINE COMPOUNDS". En III.International Scientific Congress of Pure,Appliedand Technological Sciences. Rimar Academy, 2021. http://dx.doi.org/10.47832/minarcongress3-3.
Texto completoRaposo, M. Manuela, M. Cidália Castro, R. Cristina M. Ferreira y Susana P. G. Costa. "Synthesis and evaluation of heterocyclic pyrrolidene imines as optical chemosensors". En The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a021.
Texto completoNaimi-Jamal, M. y E. Ali. "Efficient synthesis of imines by MCM-41-SO3H nanocatalyst". En The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00399.
Texto completoInformes sobre el tema "Imines"
Hall, Henry K. y Jr. Polymerization of Azaethylenes (Imines) and Aza-1,3-Dienes. Potential Reactive Monomers. Fort Belvoir, VA: Defense Technical Information Center, abril de 1988. http://dx.doi.org/10.21236/ada194717.
Texto completoChien, James C. y B. M. Gong. Poly(aryline imides) as E-Beam Resist: Sensitivity and Resolution. Fort Belvoir, VA: Defense Technical Information Center, enero de 1987. http://dx.doi.org/10.21236/ada201739.
Texto completoHall, H. K. y Jr. Synthesis and Polymerization of New Imine Monomers: Azaethylenes, Azabutadienes, and Azaallenes. Fort Belvoir, VA: Defense Technical Information Center, junio de 1996. http://dx.doi.org/10.21236/ada314001.
Texto completoDuBois, D. A. y R. H. Neilson. Addition Reactions of a Silylated Imino(Methylene)Phosphorane. Fort Belvoir, VA: Defense Technical Information Center, enero de 1989. http://dx.doi.org/10.21236/ada203987.
Texto completoGilstrap, Scott E. y Aaron Yanuzo. IMITS: Information and Clinical Technologies for the Advancement of Healthcare. Fort Belvoir, VA: Defense Technical Information Center, diciembre de 2008. http://dx.doi.org/10.21236/ada611064.
Texto completoAllred, Ronald E., Richard E. Jensen, Thomas A. Donnellan, Theotis Williams y Jr. Fiber Finishes for Improving Galvanic Resistance of Imide-Based Composites. Fort Belvoir, VA: Defense Technical Information Center, febrero de 1998. http://dx.doi.org/10.21236/ada341614.
Texto completoArcher, D. G. Thermodynamic properties of 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide. Gaithersburg, MD: National Institute of Standards and Technology, 2006. http://dx.doi.org/10.6028/nist.ir.6645.
Texto completoLoveland, Jo L., Rick Barbour, Al Krum y August C. Neitzel. Rollout and Installation of Risk Management at the IMINT Directorate, National Reconnaissance Office. Fort Belvoir, VA: Defense Technical Information Center, diciembre de 1999. http://dx.doi.org/10.21236/ada375848.
Texto completoMarks, Megan. Integrated Medical Information Technology System (IMITS): Information and Clinical Technologies for the Advancement of Healthcare. Fort Belvoir, VA: Defense Technical Information Center, agosto de 2010. http://dx.doi.org/10.21236/ada633139.
Texto completoCooke, Garth, Nicola Maiorana, Theodore Myers, Johnnie Jernigan y Eric N. Carlson. Integrated Maintenance Information System Diagnostic Module (IMIS-DM). Version 5.0. Fort Belvoir, VA: Defense Technical Information Center, junio de 1991. http://dx.doi.org/10.21236/ada237244.
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