Добірка наукової літератури з теми "Ketenimine"
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Статті в журналах з теми "Ketenimine"
Baradarani, M., RH Prager, and K. Schafer. "The Chemistry of 5-Oxodihydroisoxazoles. XV. Reaction of Derived Ketenimines With Enamines and Enolates." Australian Journal of Chemistry 49, no. 8 (1996): 911. http://dx.doi.org/10.1071/ch9960911.
Повний текст джерелаAng, KH, RH Prager, and CM Williams. "The Chemistry of 5-Oxodihydroisoxazoles. XII. Trapping of Derived Ketenimines With Lithium Amides and Alkyllithiums." Australian Journal of Chemistry 48, no. 1 (1995): 55. http://dx.doi.org/10.1071/ch9950055.
Повний текст джерелаYavari, Issa, Farough Nasiri, Hoorieh Djahaniani, and Hamid R. Bijanzadeh. "Synthesis and Dynamic NMR Study of Fluorinated Dialkyl 2-[(tert-butylimino)-methylene]-3-[(2-alkoxy-2-oxoacetyl)-2-fluoroanilino]-succinates." Journal of Chemical Research 2005, no. 8 (August 2005): 537–39. http://dx.doi.org/10.3184/030823405774663372.
Повний текст джерелаAlajarín, Mateo, Baltasar Bonillo, Pilar Sánchez-Andrada, Ángel Vidal, and Delia Bautista. "Intramolecular Ketenimine−Ketenimine [2 + 2] and [4 + 2] Cycloadditions†." Journal of Organic Chemistry 72, no. 15 (July 2007): 5863–66. http://dx.doi.org/10.1021/jo0704661.
Повний текст джерелаHe, Wenxing, Xiaojun Tan, Nana Wang, and Hong Zhang. "Theoretical study on the mechanism of the cycloaddition reaction between ketenimine and hydrogen cyanide." Journal of the Serbian Chemical Society 81, no. 2 (2016): 187–95. http://dx.doi.org/10.2298/jsc150504091h.
Повний текст джерелаBrown, RFC, KJ Coulston, and FW Eastwood. "Intramolecular Trapping of a Ketenimine Carbene Formed on Flash Vacuum Pyrolysis of 3-Phenylimino-3H-indazole and 3-Phenyliminoisobenzofuran-1-one." Australian Journal of Chemistry 47, no. 1 (1994): 47. http://dx.doi.org/10.1071/ch9940047.
Повний текст джерелаSaraví Cisneros, Hebe, Sergio Laurella, Danila L. Ruiz, Agustín Ponzinibbio, Patricia E. Allegretti, and Jorge J. P. Furlong. "Spectrometric Study of the Nitrile-Ketenimine Tautomerism." International Journal of Spectroscopy 2009 (September 9, 2009): 1–18. http://dx.doi.org/10.1155/2009/408345.
Повний текст джерелаCapuano, Lilly, and Keramatollah Djokar. "N-Funktionalisierte Ketenimine, II." Liebigs Annalen der Chemie 1985, no. 12 (December 22, 1985): 2305–12. http://dx.doi.org/10.1002/jlac.198519851202.
Повний текст джерелаCen, Mengjie, Qiaoyi Xiang, Yiwen Xu, Shengguo Duan, Yaohong Lv, Ze-Feng Xu та Chuan-Ying Li. "Synthesis of α-cyano sulfone via thermal rearrangement of 1,4-disubstituted triazole mediated by carbene and radical species". Organic Chemistry Frontiers 7, № 3 (2020): 596–601. http://dx.doi.org/10.1039/c9qo01340g.
Повний текст джерелаChauhan, Dinesh Pratapsinh, Sreejith J. Varma, Mahesh Gudem, Nihar Panigrahi, Khushboo Singh, Anirban Hazra, and Pinaki Talukdar. "Intramolecular cascade rearrangements of enynamine derived ketenimines: access to acyclic and cyclic amidines." Organic & Biomolecular Chemistry 15, no. 22 (2017): 4822–30. http://dx.doi.org/10.1039/c7ob00499k.
Повний текст джерелаДисертації з теми "Ketenimine"
Loison, Anaïs. "Synthèse et réactivité de synthons difluorométhoxylés." Electronic Thesis or Diss., Strasbourg, 2023. http://www.theses.fr/2023STRAF073.
Повний текст джерелаFluorine has demonstrated its ability to modify the physico-chemical and biological properties of molecules compared to their hydrogenated analogues, explaining its widespread use in medicinal- as well as agrochemistry. So-called Emerging Fluorinated Groups (EFG) are currently under investigation, in order to diversify the nature of the used fluorinated moieties. Therefore, we aimed to develop the synthesis of a versatile building block, namely a ketone, allowing the introduction of the OCHF2 motif. As a matter of fact, the latter possesses some interesting inherent properties, but suffers a lack of efficient introduction methods, especially on alkyl chains. First the synthesis of the difluoromethoxylated ketone was optimized. Its synthetic potential was then exploited, as it was used to access compounds such as amidines, imidates and thioimidates via a ketenimine as highly reactive specie. Subsequently, the ketone demonstrated its usefulness in accessing very rarely encountered difluoromethoxylated heterocycles, first via an enaminone intermediate, and finally directly through a Fischer-type cyclization
Revell, John Bernard. "Reactions of Some Cyclomanganated Compounds with C-Nitroso Compounds, Allenes, and Ketenimines." The University of Waikato, 2008. http://hdl.handle.net/10289/2275.
Повний текст джерелаShi, Chongsheng. "Synthesis of benzocarbazoles, indoloquinolines and indolonaphthridines from thermolysis of benzoenynyl ketenimines and carbodiimides." Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2119.
Повний текст джерелаTitle from document title page. Document formatted into pages; contains ix, 82 p. : ill. Includes abstract. Includes bibliographical references (p. 70-80).
Книги з теми "Ketenimine"
Ruane, Patrick H. The synthesis and detection of monoalkyl-aryl ketenes and ketenimines. Dublin: University College Dublin, 1997.
Знайти повний текст джерелаЧастини книг з теми "Ketenimine"
Aumann, Rudolf. "Ketenimine Complexes as Building Blocks for N-Heterocyclic and Carbocyclic Compounds." In Organometallics in Organic Synthesis, 69–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-73196-9_4.
Повний текст джерелаLappert, Michael F. "Insertion Reactions of an Isocyanate, Isothiocyanate, Carbodiimide, Ketene, Diketene, or Ketenimine." In Inorganic Reactions and Methods, 434–39. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch268.
Повний текст джерела"Ketenimine-Acetals (I)." In Substance index : from the 4th edition and the additional and supplementary volumes to the 4th edition, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114379.
Повний текст джерела"Ketenimine-Acetals (II)." In Substance index : from the 4th edition and the additional and supplementary volumes to the 4th edition, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114380.
Повний текст джерелаPerst, H. "Iminocarbene–Ketenimine Rearrangement." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00760.
Повний текст джерелаSchantl, J. G. "Synthesis from Nitriles (via Ketenimine Intermediates)." In Three Carbon-Heteroatom Bonds: Ketenes and Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00243.
Повний текст джерелаSchantl, J. G. "Addition of Chlorine to a Ketenimine." In Three Carbon-Heteroatom Bonds: Ketenes and Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00256.
Повний текст джерелаSchantl, J. G. "Thermal Rearrangement of Vinyl Azides to Ketenimine Intermediates." In Three Carbon-Heteroatom Bonds: Ketenes and Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00255.
Повний текст джерелаPerst, H. "Alk-2-enenitriles from ,,-Tris(trimethylsilyl)ketenimine and Aldehydes." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00808.
Повний текст джерела"Ketenimines." In Substance index : from the 4th edition and the additional and supplementary volumes to the 4th edition, edited by Backes, Fröhlich, and Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114376.
Повний текст джерелаТези доповідей конференцій з теми "Ketenimine"
Tschöpe, Martin, Guntram Rauhut, Sebastian Erfort, and Benjamin Schröder. "HIGH-LEVEL ROVIBRATIONAL CALCULATIONS ON KETENIMINE." In 2021 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.fc13.
Повний текст джерела