Gotowa bibliografia na temat „Aza-Diels–Alder cycloadditions”
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Artykuły w czasopismach na temat "Aza-Diels–Alder cycloadditions"
Heredia-Moya, Jorge, Daniel A. Zurita, José Eduardo Cadena-Cruz i Christian D. Alcívar-León. "Diaza-1,3-butadienes as Useful Intermediate in Heterocycles Synthesis". Molecules 27, nr 19 (9.10.2022): 6708. http://dx.doi.org/10.3390/molecules27196708.
Pełny tekst źródłaPresset, Marc, Michel Rajzmann, Guillaume Dauvergne, Jean Rodriguez i 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.
Pełny tekst źródłaSkrzyńska, Anna, Sebastian Frankowski i Łukasz Albrecht. "Cyclic 1‐Azadienes in the Organocatalytic Inverse‐Electron‐Demand Aza‐Diels‐Alder Cycloadditions". Asian Journal of Organic Chemistry 9, nr 11 (4.09.2020): 1688–700. http://dx.doi.org/10.1002/ajoc.202000332.
Pełny tekst źródłaCHEMOURI, HAFIDA, WAFAA BENCHOUK i 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 (grudzień 2006): 707–18. http://dx.doi.org/10.1142/s0219633606002581.
Pełny tekst źródłaSousa, Carlos A. D., M. Luísa C. Vale, José E. Rodríguez-Borges, Xerardo Garcia-Mera i Jesús Rodríguez-Otero. "Acid-catalyzed aza-Diels–Alder versus 1,3-dipolar cycloadditions of methyl glyoxylate oxime with cyclopentadiene". Tetrahedron Letters 49, nr 40 (wrzesień 2008): 5777–81. http://dx.doi.org/10.1016/j.tetlet.2008.07.110.
Pełny tekst źródłaMayr, Herbert, Armin R. Ofial, Jürgen Sauer i 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 (czerwiec 2000): 2013–20. http://dx.doi.org/10.1002/1099-0690(200006)2000:11<2013::aid-ejoc2013>3.0.co;2-a.
Pełny tekst źródłaBlanco-Carapia, Roberto E., Enrique A. Aguilar-Rangel, Mónica A. Rincón-Guevara, Alejandro Islas-Jácome i 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.
Pełny tekst źródłaFillion, Houda, Félix Pautet, Pascal Nebois i 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.
Pełny tekst źródłaNtirampebura, Deogratias, i 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 (wrzesień 1999): 7079–82. http://dx.doi.org/10.1016/s0040-4039(99)01444-6.
Pełny tekst źródłaPalacios, Francisco, Concepción Alonso, Patricia Amezua i 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 (marzec 2002): 1941–46. http://dx.doi.org/10.1021/jo016325v.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaThe 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
Części książek na temat "Aza-Diels–Alder cycloadditions"
Taber, Douglass. "Stereoselective C-N Ring Construction". W Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0054.
Pełny tekst źródłaStreszczenia konferencji na temat "Aza-Diels–Alder cycloadditions"
Rodríguez-Borges, José, Carlos Sousa, M. Luísa Vale i Xerardo García-Mera. "Aza-Diels-Alder versus 1,3-Dipolar Cycloadditions of Methyl Glyoxylate Oxime with Cyclopentadiene". W 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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