Gotowa bibliografia na temat „Ketenimine”
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Artykuły w czasopismach na temat "Ketenimine"
Baradarani, M., RH Prager i K. Schafer. "The Chemistry of 5-Oxodihydroisoxazoles. XV. Reaction of Derived Ketenimines With Enamines and Enolates". Australian Journal of Chemistry 49, nr 8 (1996): 911. http://dx.doi.org/10.1071/ch9960911.
Pełny tekst źródłaAng, KH, RH Prager i CM Williams. "The Chemistry of 5-Oxodihydroisoxazoles. XII. Trapping of Derived Ketenimines With Lithium Amides and Alkyllithiums". Australian Journal of Chemistry 48, nr 1 (1995): 55. http://dx.doi.org/10.1071/ch9950055.
Pełny tekst źródłaYavari, Issa, Farough Nasiri, Hoorieh Djahaniani i 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, nr 8 (sierpień 2005): 537–39. http://dx.doi.org/10.3184/030823405774663372.
Pełny tekst źródłaAlajarín, Mateo, Baltasar Bonillo, Pilar Sánchez-Andrada, Ángel Vidal i Delia Bautista. "Intramolecular Ketenimine−Ketenimine [2 + 2] and [4 + 2] Cycloadditions†". Journal of Organic Chemistry 72, nr 15 (lipiec 2007): 5863–66. http://dx.doi.org/10.1021/jo0704661.
Pełny tekst źródłaHe, Wenxing, Xiaojun Tan, Nana Wang i Hong Zhang. "Theoretical study on the mechanism of the cycloaddition reaction between ketenimine and hydrogen cyanide". Journal of the Serbian Chemical Society 81, nr 2 (2016): 187–95. http://dx.doi.org/10.2298/jsc150504091h.
Pełny tekst źródłaBrown, RFC, KJ Coulston i 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, nr 1 (1994): 47. http://dx.doi.org/10.1071/ch9940047.
Pełny tekst źródłaSaraví Cisneros, Hebe, Sergio Laurella, Danila L. Ruiz, Agustín Ponzinibbio, Patricia E. Allegretti i Jorge J. P. Furlong. "Spectrometric Study of the Nitrile-Ketenimine Tautomerism". International Journal of Spectroscopy 2009 (9.09.2009): 1–18. http://dx.doi.org/10.1155/2009/408345.
Pełny tekst źródłaCapuano, Lilly, i Keramatollah Djokar. "N-Funktionalisierte Ketenimine, II". Liebigs Annalen der Chemie 1985, nr 12 (22.12.1985): 2305–12. http://dx.doi.org/10.1002/jlac.198519851202.
Pełny tekst źródłaCen, Mengjie, Qiaoyi Xiang, Yiwen Xu, Shengguo Duan, Yaohong Lv, Ze-Feng Xu i 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, nr 3 (2020): 596–601. http://dx.doi.org/10.1039/c9qo01340g.
Pełny tekst źródłaChauhan, Dinesh Pratapsinh, Sreejith J. Varma, Mahesh Gudem, Nihar Panigrahi, Khushboo Singh, Anirban Hazra i Pinaki Talukdar. "Intramolecular cascade rearrangements of enynamine derived ketenimines: access to acyclic and cyclic amidines". Organic & Biomolecular Chemistry 15, nr 22 (2017): 4822–30. http://dx.doi.org/10.1039/c7ob00499k.
Pełny tekst źródłaRozprawy doktorskie na temat "Ketenimine"
Loison, Anaïs. "Synthèse et réactivité de synthons difluorométhoxylés". Electronic Thesis or Diss., Strasbourg, 2023. http://www.theses.fr/2023STRAF073.
Pełny tekst źródłaFluorine 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.
Pełny tekst źródłaShi, 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.
Pełny tekst źródłaTitle from document title page. Document formatted into pages; contains ix, 82 p. : ill. Includes abstract. Includes bibliographical references (p. 70-80).
Książki na temat "Ketenimine"
Ruane, Patrick H. The synthesis and detection of monoalkyl-aryl ketenes and ketenimines. Dublin: University College Dublin, 1997.
Znajdź pełny tekst źródłaCzęści książek na temat "Ketenimine"
Aumann, Rudolf. "Ketenimine Complexes as Building Blocks for N-Heterocyclic and Carbocyclic Compounds". W Organometallics in Organic Synthesis, 69–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-73196-9_4.
Pełny tekst źródłaLappert, Michael F. "Insertion Reactions of an Isocyanate, Isothiocyanate, Carbodiimide, Ketene, Diketene, or Ketenimine". W Inorganic Reactions and Methods, 434–39. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch268.
Pełny tekst źródła"Ketenimine-Acetals (I)". W Substance index : from the 4th edition and the additional and supplementary volumes to the 4th edition, redaktorzy Backes, Fröhlich i Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114379.
Pełny tekst źródła"Ketenimine-Acetals (II)". W Substance index : from the 4th edition and the additional and supplementary volumes to the 4th edition, redaktorzy Backes, Fröhlich i Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114380.
Pełny tekst źródłaPerst, H. "Iminocarbene–Ketenimine Rearrangement". W 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.
Pełny tekst źródłaSchantl, J. G. "Synthesis from Nitriles (via Ketenimine Intermediates)". W Three Carbon-Heteroatom Bonds: Ketenes and Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00243.
Pełny tekst źródłaSchantl, J. G. "Addition of Chlorine to a Ketenimine". W Three Carbon-Heteroatom Bonds: Ketenes and Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00256.
Pełny tekst źródłaSchantl, J. G. "Thermal Rearrangement of Vinyl Azides to Ketenimine Intermediates". W Three Carbon-Heteroatom Bonds: Ketenes and Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00255.
Pełny tekst źródłaPerst, H. "Alk-2-enenitriles from ,,-Tris(trimethylsilyl)ketenimine and Aldehydes". W 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.
Pełny tekst źródła"Ketenimines". W Substance index : from the 4th edition and the additional and supplementary volumes to the 4th edition, redaktorzy Backes, Fröhlich i Padeken. Stuttgart: Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114376.
Pełny tekst źródłaStreszczenia konferencji na temat "Ketenimine"
Tschöpe, Martin, Guntram Rauhut, Sebastian Erfort i Benjamin Schröder. "HIGH-LEVEL ROVIBRATIONAL CALCULATIONS ON KETENIMINE". W 2021 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.fc13.
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