Gotowa bibliografia na temat „N-Aryl aldimines”
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Artykuły w czasopismach na temat "N-Aryl aldimines"
Beng, Timothy K., Jorge Garcia, Jane Eichwald i 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, nr 21 (2023): 14355–60. http://dx.doi.org/10.1039/d3ra01812a.
Pełny tekst źródłaDenmark, Scott, i Hyung Chi. "Synthesis of 2-Alkenyl-Tethered Anilines". Synthesis 49, nr 13 (4.05.2017): 2873–88. http://dx.doi.org/10.1055/s-0036-1589002.
Pełny tekst źródłaLi, Yang, Bi-Jie Li, Wen-Hua Wang, Wei-Ping Huang, Xi-Sha Zhang, Kang Chen i Zhang-Jie Shi. "Rhodium-Catalyzed Direct Addition of Aryl CH Bonds to N-Sulfonyl Aldimines". Angewandte Chemie International Edition 50, nr 9 (26.01.2011): 2115–19. http://dx.doi.org/10.1002/anie.201007464.
Pełny tekst źródłaLi, Yang, Bi-Jie Li, Wen-Hua Wang, Wei-Ping Huang, Xi-Sha Zhang, Kang Chen i Zhang-Jie Shi. "Rhodium-Catalyzed Direct Addition of Aryl CH Bonds to N-Sulfonyl Aldimines". Angewandte Chemie 123, nr 9 (26.01.2011): 2163–67. http://dx.doi.org/10.1002/ange.201007464.
Pełny tekst źródłaSeth, Dipravath Kumar, i Samaresh Bhattacharya. "Copper(I) complexes of N-(aryl)pyridine-2-aldimines: Spectral, electrochemical and catalytic properties". Polyhedron 30, nr 15 (wrzesień 2011): 2438–43. http://dx.doi.org/10.1016/j.poly.2011.05.037.
Pełny tekst źródłaLi, Yang, Bi-Jie Li, Wen-Hua Wang, Wei-Ping Huang, Xi-Sha Zhang, Kang Chen i Zhang-Jie Shi. "ChemInform Abstract: Rhodium-Catalyzed Direct Addition of Aryl C-H Bonds to N-Sulfonyl Aldimines." ChemInform 42, nr 26 (3.06.2011): no. http://dx.doi.org/10.1002/chin.201126087.
Pełny tekst źródłaZhao, Gui-Ling, i Min Shi. "Baylis–Hillman reactions of N-tosyl aldimines and aryl aldehydes with 3-methylpenta-3,4-dien-2-one". Organic & Biomolecular Chemistry 3, nr 20 (2005): 3686. http://dx.doi.org/10.1039/b510572b.
Pełny tekst źródłaPaul, Piyali, i 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 (sierpień 2012): 72–79. http://dx.doi.org/10.1016/j.jorganchem.2012.04.023.
Pełny tekst źródłaMitra, Kamala, Subhendu Biswas, Shyamal Kumar Chattopadhyay, C. Robert Lucas i 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, nr 8 (21.06.2007): 567–71. http://dx.doi.org/10.1007/s10870-007-9212-y.
Pełny tekst źródłaCurti, Claudio, Lucia Battistini, Beatrice Ranieri, Giorgio Pelosi, Gloria Rassu, Giovanni Casiraghi i Franca Zanardi. "ChemInform Abstract: anti-Selective, Catalytic Asymmetric Vinylogous Mukaiyama Mannich Reactions of Pyrrole-Based Silyl Dienolates with N-Aryl Aldimines." ChemInform 42, nr 27 (9.06.2011): no. http://dx.doi.org/10.1002/chin.201127115.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
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