Letteratura scientifica selezionata sul tema "Imines"
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Articoli di riviste sul tema "Imines"
Svete, Jurij, Uroš Grošelj, Franc Požgan e Bogdan Štefane. "Copper-Catalyzed Azomethine Imine–Alkyne Cycloadditions (CuAIAC)". Synthesis 50, n. 23 (5 ottobre 2018): 4501–24. http://dx.doi.org/10.1055/s-0037-1610284.
Testo completoWulff, William, Xin Zhang e Yijing Dai. "The Acceleration of the Rearrangement of α-Hydroxy Aldimines by Lewis or Brønsted Acids". Synlett 29, n. 15 (28 agosto 2018): 2015–18. http://dx.doi.org/10.1055/s-0037-1610262.
Testo 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. 24 (13 dicembre 2019): 4191. http://dx.doi.org/10.3390/ma12244191.
Testo completoMendes, Joseane A., Paulo R. R. Costa, Miguel Yus, Francisco Foubelo e Camilla D. Buarque. "N-tert-Butanesulfinyl imines in the asymmetric synthesis of nitrogen-containing heterocycles". Beilstein Journal of Organic Chemistry 17 (12 maggio 2021): 1096–140. http://dx.doi.org/10.3762/bjoc.17.86.
Testo completoGarrido-Castro, Alberto F., M. Carmen Maestro e José Alemán. "α-Functionalization of Imines via Visible Light Photoredox Catalysis". Catalysts 10, n. 5 (19 maggio 2020): 562. http://dx.doi.org/10.3390/catal10050562.
Testo completoNugent, Thomas C., Richard Vaughan Williams, Andrei Dragan, Alejandro Alvarado Méndez e 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 ottobre 2013): 2103–12. http://dx.doi.org/10.3762/bjoc.9.247.
Testo completoRawaa Daoud Sulaiman e 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. 4 (28 novembre 2022): 31–38. http://dx.doi.org/10.25130/tjps.v27i4.30.
Testo completoAn, Ran, Mengbi Guo, Yingbo Zang, Hang Xu, Zhuang Hou e Chun Guo. "Recent Advances in Synthesis of Benzazoles via Imines". Current Organic Chemistry 24, n. 17 (12 novembre 2020): 1897–942. http://dx.doi.org/10.2174/1385272824999200818180845.
Testo completoFreese, Tyll, Jan C. Namyslo, Martin Nieger e Andreas Schmidt. "Sulfur, mercury, and boron adducts of sydnone imine derived anionic N-heterocyclic carbenes". RSC Advances 9, n. 9 (2019): 4781–88. http://dx.doi.org/10.1039/c9ra00294d.
Testo completoZhang, Hanmo, E. Ben Hay, Stephen J. Geib e Dennis P. Curran. "Fates of imine intermediates in radical cyclizations of N-sulfonylindoles and ene-sulfonamides". Beilstein Journal of Organic Chemistry 11 (17 settembre 2015): 1649–55. http://dx.doi.org/10.3762/bjoc.11.181.
Testo completoTesi sul 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.
Testo completoYoung, Adrian R. "Free radical cyclisation of imines". Thesis, Loughborough University, 1996. https://dspace.lboro.ac.uk/2134/15357.
Testo completoTillman, Anna Louise. "Organocatalytic, enantioselective additions to imines". Thesis, University of Cambridge, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612994.
Testo 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.
Testo 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.
Testo 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.
Testo 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.
Testo 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.
Testo completoGuillemin, Jean-Claude. "Les imines non-stabilisees : synthese et reactivite". Rennes 1, 1986. http://www.theses.fr/1986REN10053.
Testo completoGuillemin, Jean-Claude. "Les Imines non-stabilisées synthèse et réactivité". Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37598084v.
Testo completoLibri sul tema "Imines"
Johnson, A. William. Ylides and imines of phosphorus. New York: Wiley, 1993.
Cerca il testo completoKimpe, Norbert De. The chemistry of &-haloketones, &-haloaldehydes and &-haloimines. Chichester, England: Wiley, 1988.
Cerca il testo completoHartley, James Holroyd. Saccharide accelerated hydrolysis of boronic acid imines. Birmingham: University of Birmingham, 2000.
Cerca il testo completoKimpe, Norbert de. The chemistry of [alpha]-haloketones, [alpha]-haloaldehydes, and [alpha]-haloimines. Chichester: Wiley, 1988.
Cerca il testo completoHallett, David James. Ally lstannanes: Reaction with imines, iminium ions and ketones. Manchester: University of Manchester, 1993.
Cerca il testo completoRahid, H. S. New syntheses of imines and chiral B-aminophosphine derivatives. Manchester: UMIST, 1997.
Cerca il testo completoPower, Nicholas Patrick. Kinetics and mechanisms of reactions of N-Arylsulfonyl derivatives of imines. [S.l: The Author], 1998.
Cerca il testo completoCenter, Langley Research, a cura di. Modified phenylethynyl containing imides for secondary bonding: Non-autoclave, low twmperature processable adhesives. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1999.
Cerca il testo completoMazurkiewicz, Roman. Studium reakcji imidoilowania amidów. Gliwice: Politechnika Śląska, 1989.
Cerca il testo completoCenter, Langley Research, e United States. National Aeronautics and Space Administration., a cura di. Synthesis and characterization of modified phenylethynyl terminated polyimides. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1998.
Cerca il testo completoCapitoli di libri sul tema "Imines"
Rowlands, C. C., e R. D. Farley. "15.7.2 Imines and imides". In 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.
Testo completoDilworth, J. R., e S. Morton. "From Imines". In Inorganic Reactions and Methods, 41–43. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch25.
Testo completoOjima, I. "Of Imines". In Inorganic Reactions and Methods, 255–57. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145319.ch83.
Testo completoLi, Wei, e Xumu Zhang. "Asymmetric Hydrogenation of Imines". In Stereoselective Formation of Amines, 103–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/128_2013_483.
Testo completoMartin, Dean F., e Edward J. Olszewski. "Metal Derivatives of β-Keto Imines (β-Imino Ketones)". In Inorganic Syntheses, 45–52. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132395.ch14.
Testo completoSharp, John T. "Nitrile Ylides and Nitrile Imines". In 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.
Testo completoVilariño, Natalia, Sara F. Ferreiro, Andrés Crespo e José Gil. "Pharmacology of the cyclic imines". In Phycotoxins, 343–60. Chichester, UK: John Wiley & Sons, Ltd, 2015. http://dx.doi.org/10.1002/9781118500354.ch15.
Testo completoBailey, Patrick D., e Keith M. Morgan. "Enamines". In Organonitrogen Chemistry. Oxford University Press, 2022. http://dx.doi.org/10.1093/hesc/9780198557753.003.0008.
Testo completoSandler, Stanley R., e Wolf Karo. "IMINES". In Sourcebook of Advanced Organic Laboratory Preparations, 234–36. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-08-092553-0.50035-2.
Testo completoSandler, Stanley R., e Wolf Karo. "IMINES". In Organic Functional Group Preparations, 291–322. Elsevier, 1986. http://dx.doi.org/10.1016/b978-0-08-092557-8.50016-1.
Testo completoAtti di convegni sul tema "Imines"
Mas-Marzá, Elena, Ramón Arcas-Martínez, Laxman Gouda e Francisco Fabregat-Santiago. "Photoelectrosynthesis of Imines". In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.ngfm.2019.271.
Testo completoMas-Marzá, Elena, Ramón Arcas-Martínez, Laxman Gouda e Francisco Fabregat-Santiago. "Photoelectrosynthesis of Imines". In nanoGe Fall Meeting 2019. València: Fundació Scito, 2019. http://dx.doi.org/10.29363/nanoge.nfm.2019.271.
Testo completoPinho e Melo, Teresa, Ana Cabral e António d'A Rocha Gonsalves. "Intramolecular Cycloaddition of Imines of Cysteine Derivatives". In The 1st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02044.
Testo completoMargulï¾s, L., J. C. Guillemin, Brett McGuire, Anthony Remijan, Olga Dorovskaya, V. Ilyushin e R. Motiyenko. "SUBMILLIMETER WAVE SPECTROSCOPY FOR ISM: IMINES WITH INTERNAL ROTATION". In 74th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.tg05.
Testo completoDiz-Gil, Raquel, Sara Bermúdez-Fernández, Paula Munín-Cruz, María Pereira e José Vila. "Preparation and crystal structure of metallated 2,4,6-trimethylaniline imines". In The 24th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08322.
Testo completoShutalev, Anatoly. "A New Approach to the Synthesis of Hydrogenated Pyrimidine-2-imines". In The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01854.
Testo completoRaposo, M. Manuela, e M. Cidália Castro. "Synthesis and Characterization of the Photophysical Properties of Novel Heterocyclic Imines". In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a048.
Testo completoMOHSIN, Doaa Hadi, e Zahraa Hameed KAMIL. "SYNTHESIS AND CHARACTERIZATION OF SOME NEW 1,3-OXAZEPINE COMPOUNDS". In III.International Scientific Congress of Pure,Appliedand Technological Sciences. Rimar Academy, 2021. http://dx.doi.org/10.47832/minarcongress3-3.
Testo completoRaposo, M. Manuela, M. Cidália Castro, R. Cristina M. Ferreira e Susana P. G. Costa. "Synthesis and evaluation of heterocyclic pyrrolidene imines as optical chemosensors". In The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a021.
Testo completoNaimi-Jamal, M., e E. Ali. "Efficient synthesis of imines by MCM-41-SO3H nanocatalyst". In The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00399.
Testo completoRapporti di organizzazioni sul tema "Imines"
Hall, Henry K., e Jr. Polymerization of Azaethylenes (Imines) and Aza-1,3-Dienes. Potential Reactive Monomers. Fort Belvoir, VA: Defense Technical Information Center, aprile 1988. http://dx.doi.org/10.21236/ada194717.
Testo completoChien, James C., e B. M. Gong. Poly(aryline imides) as E-Beam Resist: Sensitivity and Resolution. Fort Belvoir, VA: Defense Technical Information Center, gennaio 1987. http://dx.doi.org/10.21236/ada201739.
Testo completoHall, H. K., e Jr. Synthesis and Polymerization of New Imine Monomers: Azaethylenes, Azabutadienes, and Azaallenes. Fort Belvoir, VA: Defense Technical Information Center, giugno 1996. http://dx.doi.org/10.21236/ada314001.
Testo completoDuBois, D. A., e R. H. Neilson. Addition Reactions of a Silylated Imino(Methylene)Phosphorane. Fort Belvoir, VA: Defense Technical Information Center, gennaio 1989. http://dx.doi.org/10.21236/ada203987.
Testo completoGilstrap, Scott E., e Aaron Yanuzo. IMITS: Information and Clinical Technologies for the Advancement of Healthcare. Fort Belvoir, VA: Defense Technical Information Center, dicembre 2008. http://dx.doi.org/10.21236/ada611064.
Testo completoAllred, Ronald E., Richard E. Jensen, Thomas A. Donnellan, Theotis Williams e Jr. Fiber Finishes for Improving Galvanic Resistance of Imide-Based Composites. Fort Belvoir, VA: Defense Technical Information Center, febbraio 1998. http://dx.doi.org/10.21236/ada341614.
Testo 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.
Testo completoLoveland, Jo L., Rick Barbour, Al Krum e August C. Neitzel. Rollout and Installation of Risk Management at the IMINT Directorate, National Reconnaissance Office. Fort Belvoir, VA: Defense Technical Information Center, dicembre 1999. http://dx.doi.org/10.21236/ada375848.
Testo 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 2010. http://dx.doi.org/10.21236/ada633139.
Testo completoCooke, Garth, Nicola Maiorana, Theodore Myers, Johnnie Jernigan e Eric N. Carlson. Integrated Maintenance Information System Diagnostic Module (IMIS-DM). Version 5.0. Fort Belvoir, VA: Defense Technical Information Center, giugno 1991. http://dx.doi.org/10.21236/ada237244.
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