Literatura científica selecionada sobre o tema "Aza-Diels–Alder cycloadditions"
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Artigos de revistas sobre o assunto "Aza-Diels–Alder cycloadditions"
Heredia-Moya, Jorge, Daniel A. Zurita, José Eduardo Cadena-Cruz e Christian D. Alcívar-León. "Diaza-1,3-butadienes as Useful Intermediate in Heterocycles Synthesis". Molecules 27, n.º 19 (9 de outubro de 2022): 6708. http://dx.doi.org/10.3390/molecules27196708.
Texto completo da fontePresset, Marc, Michel Rajzmann, Guillaume Dauvergne, Jean Rodriguez e Yoann Coquerel. "Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study". Molecules 25, n.º 20 (20 de outubro de 2020): 4811. http://dx.doi.org/10.3390/molecules25204811.
Texto completo da fonteSkrzyńska, Anna, Sebastian Frankowski e Łukasz Albrecht. "Cyclic 1‐Azadienes in the Organocatalytic Inverse‐Electron‐Demand Aza‐Diels‐Alder Cycloadditions". Asian Journal of Organic Chemistry 9, n.º 11 (4 de setembro de 2020): 1688–700. http://dx.doi.org/10.1002/ajoc.202000332.
Texto completo da fonteCHEMOURI, HAFIDA, WAFAA BENCHOUK e 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, n.º 04 (dezembro de 2006): 707–18. http://dx.doi.org/10.1142/s0219633606002581.
Texto completo da fonteSousa, Carlos A. D., M. Luísa C. Vale, José E. Rodríguez-Borges, Xerardo Garcia-Mera e Jesús Rodríguez-Otero. "Acid-catalyzed aza-Diels–Alder versus 1,3-dipolar cycloadditions of methyl glyoxylate oxime with cyclopentadiene". Tetrahedron Letters 49, n.º 40 (setembro de 2008): 5777–81. http://dx.doi.org/10.1016/j.tetlet.2008.07.110.
Texto completo da fonteMayr, Herbert, Armin R. Ofial, Jürgen Sauer e Bernhard Schmied. "[2++4] Cycloadditions of Iminium Ions − Concerted or Stepwise Mechanism of Aza Diels−Alder Reactions?" European Journal of Organic Chemistry 2000, n.º 11 (junho de 2000): 2013–20. http://dx.doi.org/10.1002/1099-0690(200006)2000:11<2013::aid-ejoc2013>3.0.co;2-a.
Texto completo da fonteBlanco-Carapia, Roberto E., Enrique A. Aguilar-Rangel, Mónica A. Rincón-Guevara, Alejandro Islas-Jácome e Eduardo González-Zamora. "Synthesis of New Polyheterocyclic Pyrrolo[3,4-b]pyridin-5-ones via an Ugi-Zhu/Cascade/Click Strategy". Molecules 28, n.º 10 (14 de maio de 2023): 4087. http://dx.doi.org/10.3390/molecules28104087.
Texto completo da fonteFillion, Houda, Félix Pautet, Pascal Nebois e Zouhair Bouaziz. "Cycloadditions of α,β-Unsaturated N,N-Dimethylhydrazones. A Diels-Alder Strategy for the Building of Aza-Hetero Rings". HETEROCYCLES 54, n.º 2 (2001): 1095. http://dx.doi.org/10.3987/rev-00-sr(i)5.
Texto completo da fonteNtirampebura, Deogratias, e 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, n.º 39 (setembro de 1999): 7079–82. http://dx.doi.org/10.1016/s0040-4039(99)01444-6.
Texto completo da fontePalacios, Francisco, Concepción Alonso, Patricia Amezua e 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, n.º 6 (março de 2002): 1941–46. http://dx.doi.org/10.1021/jo016325v.
Texto completo da fonteTeses / dissertações sobre o assunto "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.
Texto completo da fonteThe 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
Capítulos de livros sobre o assunto "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.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Aza-Diels–Alder cycloadditions"
Rodríguez-Borges, José, Carlos Sousa, M. Luísa Vale e 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.
Texto completo da fonte