Auswahl der wissenschaftlichen Literatur zum Thema „Aza-Diels–Alder cycloadditions“
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Zeitschriftenartikel zum Thema "Aza-Diels–Alder cycloadditions"
Heredia-Moya, Jorge, Daniel A. Zurita, José Eduardo Cadena-Cruz und Christian D. Alcívar-León. „Diaza-1,3-butadienes as Useful Intermediate in Heterocycles Synthesis“. Molecules 27, Nr. 19 (09.10.2022): 6708. http://dx.doi.org/10.3390/molecules27196708.
Der volle Inhalt der QuellePresset, Marc, Michel Rajzmann, Guillaume Dauvergne, Jean Rodriguez und Yoann Coquerel. „Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study“. Molecules 25, Nr. 20 (20.10.2020): 4811. http://dx.doi.org/10.3390/molecules25204811.
Der volle Inhalt der QuelleSkrzyńska, Anna, Sebastian Frankowski und Łukasz Albrecht. „Cyclic 1‐Azadienes in the Organocatalytic Inverse‐Electron‐Demand Aza‐Diels‐Alder Cycloadditions“. Asian Journal of Organic Chemistry 9, Nr. 11 (04.09.2020): 1688–700. http://dx.doi.org/10.1002/ajoc.202000332.
Der volle Inhalt der QuelleCHEMOURI, HAFIDA, WAFAA BENCHOUK und SIDI MOHAMED MEKELLECHE. „REGIOSELECTIVITY OF HETERO DIELS–ALDER REACTIONS BETWEEN 1-AZA-1,3-BUTADIENE DERIVATIVES AND DIMETHYLVINYLAMINE: A THEORETICAL INVESTIGATION“. Journal of Theoretical and Computational Chemistry 05, Nr. 04 (Dezember 2006): 707–18. http://dx.doi.org/10.1142/s0219633606002581.
Der volle Inhalt der QuelleSousa, Carlos A. D., M. Luísa C. Vale, José E. Rodríguez-Borges, Xerardo Garcia-Mera und Jesús Rodríguez-Otero. „Acid-catalyzed aza-Diels–Alder versus 1,3-dipolar cycloadditions of methyl glyoxylate oxime with cyclopentadiene“. Tetrahedron Letters 49, Nr. 40 (September 2008): 5777–81. http://dx.doi.org/10.1016/j.tetlet.2008.07.110.
Der volle Inhalt der QuelleMayr, Herbert, Armin R. Ofial, Jürgen Sauer und Bernhard Schmied. „[2++4] Cycloadditions of Iminium Ions − Concerted or Stepwise Mechanism of Aza Diels−Alder Reactions?“ European Journal of Organic Chemistry 2000, Nr. 11 (Juni 2000): 2013–20. http://dx.doi.org/10.1002/1099-0690(200006)2000:11<2013::aid-ejoc2013>3.0.co;2-a.
Der volle Inhalt der QuelleBlanco-Carapia, Roberto E., Enrique A. Aguilar-Rangel, Mónica A. Rincón-Guevara, Alejandro Islas-Jácome und Eduardo González-Zamora. „Synthesis of New Polyheterocyclic Pyrrolo[3,4-b]pyridin-5-ones via an Ugi-Zhu/Cascade/Click Strategy“. Molecules 28, Nr. 10 (14.05.2023): 4087. http://dx.doi.org/10.3390/molecules28104087.
Der volle Inhalt der QuelleFillion, Houda, Félix Pautet, Pascal Nebois und Zouhair Bouaziz. „Cycloadditions of α,β-Unsaturated N,N-Dimethylhydrazones. A Diels-Alder Strategy for the Building of Aza-Hetero Rings“. HETEROCYCLES 54, Nr. 2 (2001): 1095. http://dx.doi.org/10.3987/rev-00-sr(i)5.
Der volle Inhalt der QuelleNtirampebura, Deogratias, und Léon Ghosez. „Cycloadditions of 2-aza-1,3-dienes to aldehydes: a Diels-Alder strategy for the diastereoselective hydroxyalkylation of carboxylic acid derivatives“. Tetrahedron Letters 40, Nr. 39 (September 1999): 7079–82. http://dx.doi.org/10.1016/s0040-4039(99)01444-6.
Der volle Inhalt der QuellePalacios, Francisco, Concepción Alonso, Patricia Amezua und Gloria Rubiales. „Synthesis of Aza Polycyclic Compounds Derived from Pyrrolidine, Indolizidine, and Indole via Intramolecular Diels−Alder Cycloadditions of Neutral 2-Azadienes“. Journal of Organic Chemistry 67, Nr. 6 (März 2002): 1941–46. http://dx.doi.org/10.1021/jo016325v.
Der volle Inhalt der QuelleDissertationen zum Thema "Aza-Diels–Alder cycloadditions"
Castro, Agudelo Brian Alejandro. „Arynes as short-lived intermediates for the synthesis of nucleosides and N-doped PAHs“. Electronic Thesis or Diss., Aix-Marseille, 2021. http://www.theses.fr/2021AIXM0182.
Der volle Inhalt der QuelleThe chemistry of ortho-arynes, that are arenes containing formally a triple bond inthe aromatic ring, has experienced a renewed interest in the last decade. Arynes areelectrophilic species with high reactivity precluding their isolation but allowing their reaction with a number of arynophiles. In this manuscript we present the current trends in aryne chemistry and our own work in the field. The aim of our work was to explore the use of the aza-Diels–Alder cycloaddition between arynes and aldimines asa synthetic tool to elaborate original molecular architectures for applications indifferent fields, from medicinal chemistry to materials. In a first approach, some one pot aza Diels-Alder cycloaddition / oxidation sequences were developed for the synthesis of protected benzo[e]-7-azaindoles, which were converted to nucleosides by coupling reaction with ribose derivatives. The antiviral activity of these molecules is under investigation. In another approach some cascade aza-Diels–Aldercycloaddition / N-arylation sequences were developed for the synthesis of N-arylated hydroisoquinolines, which were converted into cationic N-doped axially chiralpolyaromatic hydrocarbons. Some of their physicochemical properties were evaluated by spectroscopy and computational modeling. Over all this work indicates that arynes may not yet have revealed their full potential in synthesis
Buchteile zum Thema "Aza-Diels–Alder cycloadditions"
Taber, Douglass. „Stereoselective C-N Ring Construction“. In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0054.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Aza-Diels–Alder cycloadditions"
Rodríguez-Borges, José, Carlos Sousa, M. Luísa Vale und Xerardo García-Mera. „Aza-Diels-Alder versus 1,3-Dipolar Cycloadditions of Methyl Glyoxylate Oxime with Cyclopentadiene“. In The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01218.
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