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Pure Appl. Chem., 1996, Vol. 68, No. 4, pp. 859-862

http://dx.doi.org/10.1351/pac199668040859

The use of 2-azadienes in the Diels-Alder reaction

T. L. Gilchrist, A. M. d'A. R. Gonsalves and T. M. V. D. Pinho e Melo

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  • Al-Awadi Nouria A., Ibrahim Yehia A., John Elizabeth, Parveen Aneesha: Pyrolysis of 3-hydroxy-2-arylhydrazonoalkanoic acid derivatives. Tetrahedron 2011, 67, 1298. <http://dx.doi.org/10.1016/j.tet.2010.11.074>
  • Monbaliu Jean-Christophe M., Masschelein Kurt G. R., Stevens Christian V.: Electron-deficient 1- and 2-azabuta-1,3-dienes: a comprehensive survey of their synthesis and reactivity. Chem Soc Rev 2011, 40, 4708. <http://dx.doi.org/10.1039/c1cs15070g>
  • Palacios Francisco, Marigorta Edorta Martínez de, Rodríguez Marta, Vinagre Carmen: Synthesis and Reactivity of an 1,3-Oxazin-6-one Derived from α-Aminophosphonate. Phosphorus Sulfur Silicon Relat Elements 2011, 186, 729. <http://dx.doi.org/10.1080/10426507.2010.522633>
  • GILCHRIST T. L., ROCHA GONSALVES A. M. D'A., PINHO E MELO T. M. V. D.: ChemInform Abstract: The Use of 2-Azadienes in the Diels-Alder Reaction. ChemInform 2010, 27, no. <http://dx.doi.org/10.1002/chin.199650270>
  • Bongini Alessandro, Panunzio Mauro, Venturini Alessandro: Silyloxyazadienes: one intermediate and two competitive pericyclic reactions. Phys Chem Chem Phys 2010, 12, 5067. <http://dx.doi.org/10.1039/b925351c>
  • Yavari Issa, Karimi Elham: Synthesis of Functionalized 1‐Azadienes by Reaction of 2,6‐Dimethylphenyl Isocyanide and Acetylenic Esters in the Presence of CH Acids. Synth Comm 2007, 37, 1189. <http://dx.doi.org/10.1080/00397910701199086>
  • Deryabina Tatyana G., Belskaia Natalia P., Kodess Michail I., Dehaen Wim, Toppet Suzanne, Bakulev Vasiliy A.: [3+2]- Versus [4+2]-cycloaddition reactions of 3-methylsulfanyl-2-arylazo-3-(pyrrolidin-1-yl)acrylonitriles with N-substituted maleimides involving pyrrolidine-derived azomethine ylides. Tetrahetron Lett 2006, 47, 1853. <http://dx.doi.org/10.1016/j.tetlet.2005.12.130>
  • Sisak Attila: New Method for the Synthesis of 2‐Aza‐1,3‐Butadienes. Synth Comm 2006, 36, 3693. <http://dx.doi.org/10.1080/00397910600946033>
  • Rubiales Gloria, Ezpeleta Jose María, Palacios Francisco, Alonso Concepción: Cycloaddition Reactions of Neutral 2-Azadienes with Enamines − Regiospecific Synthesis of Highly Substituted Dihydropyridines and Pyridines. Eur J Org Chem 2001, 2001, 2115. <http://dx.doi.org/10.1002/1099-0690(200106)2001:11<2115::AID-EJOC2115>3.0.CO;2-P>
  • Palacios Francisco, Aparicio Domitila, Garcı́a Jesús, Rodrı́guez Encina, Fernández-Acebes Alvaro: A convenient synthesis of racemic and optically active 1-aza-1,3-dienes derived from γ-amino esters: reduction to α,β-unsaturated and saturated γ-amino acid derivatives. Tetrahedron 2001, 57, 3131. <http://dx.doi.org/10.1016/S0040-4020(01)00171-5>
  • Boeckman, Robert K., Ge Ping, Reed Jessica E.: New Heterocyclic Precursors for Thermal Generation of Reactive, Electron-Rich 1,2-Diaza-1,3-butadienes. Org Lett 2001, 3, 3647. <http://dx.doi.org/10.1021/ol0165645>
  • Paparin Jean-Laurent, Crévisy Christophe, Grée René, Toupet Loïc: Synthesis of 2,5- bis -arylpyridines by [4 + 2] cycloaddition of 1,4-bis aryl-2-aza-1,3-butadienes with electron-poor dienophiles. Journal of Heterocyclic Chemistry 2000, 37, 411. <http://dx.doi.org/10.1002/jhet.5570370230>
  • Palacios Francisco, Gil Marie J., de Marigorta Eduardo Martínez, Rodríguez Marta: Synthesis of 3-phosphorylated 2-aza-1,3-dienes from imines derived from bisphosphonates. Tetrahetron Lett 1999, 40, 2411. <http://dx.doi.org/10.1016/S0040-4039(99)00116-1>
  • Vogt Paul F., Miller Marvin J.: Development and applications of amino acid-derived chiral acylnitroso hetero Diels-Alder reactions. Tetrahedron 1998, 54, 1317. <http://dx.doi.org/10.1016/S0040-4020(97)10072-2>
  • Béres Mariann, Hajós György, Riedl Zsuzsanna, Timári Géza, Messmer András, Holly Sándor, Schantl Joachim G.: Ring opening of [1,2,3]triazolo[1,5-a]pyrazinium salts: Synthesis and some transformations of a novel type of 2-aza-1,3-butadienes. Tetrahedron 1997, 53, 9393. <http://dx.doi.org/10.1016/S0040-4020(97)00591-7>