Literatura científica selecionada sobre o tema "N-Aryl aldimines"
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Artigos de revistas sobre o assunto "N-Aryl aldimines"
Beng, Timothy K., Jorge Garcia, Jane Eichwald e Claire Borg. "Introducing a sulfone-embedded anhydride to the anhydride-imine reaction for the modular synthesis of N-heterocyclic sulfones bearing vicinal stereocenters". RSC Advances 13, n.º 21 (2023): 14355–60. http://dx.doi.org/10.1039/d3ra01812a.
Texto completo da fonteDenmark, Scott, e Hyung Chi. "Synthesis of 2-Alkenyl-Tethered Anilines". Synthesis 49, n.º 13 (4 de maio de 2017): 2873–88. http://dx.doi.org/10.1055/s-0036-1589002.
Texto completo da fonteLi, Yang, Bi-Jie Li, Wen-Hua Wang, Wei-Ping Huang, Xi-Sha Zhang, Kang Chen e Zhang-Jie Shi. "Rhodium-Catalyzed Direct Addition of Aryl CH Bonds to N-Sulfonyl Aldimines". Angewandte Chemie International Edition 50, n.º 9 (26 de janeiro de 2011): 2115–19. http://dx.doi.org/10.1002/anie.201007464.
Texto completo da fonteLi, Yang, Bi-Jie Li, Wen-Hua Wang, Wei-Ping Huang, Xi-Sha Zhang, Kang Chen e Zhang-Jie Shi. "Rhodium-Catalyzed Direct Addition of Aryl CH Bonds to N-Sulfonyl Aldimines". Angewandte Chemie 123, n.º 9 (26 de janeiro de 2011): 2163–67. http://dx.doi.org/10.1002/ange.201007464.
Texto completo da fonteSeth, Dipravath Kumar, e Samaresh Bhattacharya. "Copper(I) complexes of N-(aryl)pyridine-2-aldimines: Spectral, electrochemical and catalytic properties". Polyhedron 30, n.º 15 (setembro de 2011): 2438–43. http://dx.doi.org/10.1016/j.poly.2011.05.037.
Texto completo da fonteLi, Yang, Bi-Jie Li, Wen-Hua Wang, Wei-Ping Huang, Xi-Sha Zhang, Kang Chen e Zhang-Jie Shi. "ChemInform Abstract: Rhodium-Catalyzed Direct Addition of Aryl C-H Bonds to N-Sulfonyl Aldimines." ChemInform 42, n.º 26 (3 de junho de 2011): no. http://dx.doi.org/10.1002/chin.201126087.
Texto completo da fonteZhao, Gui-Ling, e Min Shi. "Baylis–Hillman reactions of N-tosyl aldimines and aryl aldehydes with 3-methylpenta-3,4-dien-2-one". Organic & Biomolecular Chemistry 3, n.º 20 (2005): 3686. http://dx.doi.org/10.1039/b510572b.
Texto completo da fontePaul, Piyali, e Samaresh Bhattacharya. "Iridium mediated N–H and C–H bond activation of N-(aryl)pyrrole-2-aldimines. Synthesis, structure and, spectral and electrochemical properties". Journal of Organometallic Chemistry 713 (agosto de 2012): 72–79. http://dx.doi.org/10.1016/j.jorganchem.2012.04.023.
Texto completo da fonteMitra, Kamala, Subhendu Biswas, Shyamal Kumar Chattopadhyay, C. Robert Lucas e Bibhutosh Adhikary. "Synthesis and X-ray Crystal Structures of Two Luminescent Imidazopyridinium Derivatives from the Corresponding N-(aryl)-Pyridine-2-aldimines". Journal of Chemical Crystallography 37, n.º 8 (21 de junho de 2007): 567–71. http://dx.doi.org/10.1007/s10870-007-9212-y.
Texto completo da fonteCurti, Claudio, Lucia Battistini, Beatrice Ranieri, Giorgio Pelosi, Gloria Rassu, Giovanni Casiraghi e Franca Zanardi. "ChemInform Abstract: anti-Selective, Catalytic Asymmetric Vinylogous Mukaiyama Mannich Reactions of Pyrrole-Based Silyl Dienolates with N-Aryl Aldimines." ChemInform 42, n.º 27 (9 de junho de 2011): no. http://dx.doi.org/10.1002/chin.201127115.
Texto completo da fonteTeses / dissertações sobre o assunto "N-Aryl aldimines"
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