Relevant bibliographies by topics / N-Aryl aldimines

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Academic literature on the topic 'N-Aryl aldimines'

Author: Grafiati
Published: 25 May 2024
Last updated: 31 July 2025

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Journal articles on the topic "N-Aryl aldimines"

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Beng, Timothy K., Jorge Garcia, Jane Eichwald, and 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, no. 21 (2023): 14355–60. http://dx.doi.org/10.1039/d3ra01812a.

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Rohit, Kumar, Paul Piyali, and Bhattacharya Samaresh. "N-(Aryl)pyrrole-2-aldimine complexes of ruthenium: Synthesis, characterization and catalytic transfer-hydrogenation." Journal of Indian Chemical Society Vol. 95, Jul 2018 (2018): 721–28. https://doi.org/10.5281/zenodo.5638362.

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Department of Chemistry, Inorganic Chemistry Section, Jadavpur University, Kolkata-700 032, India <em>E</em>-<em>mail:</em> samaresh_b@hotmail.com <em>Manuscript received 28 June 2018, accepted 10 July 2018</em> Reaction of N-(4&#39;-R-phenyl)pyrrole-2-aldimines (HL-R, where H represents the acidic N-H hydrogen and, R = OCH<sub>3</sub>, CH<sub>3</sub>, H and CI) with [Ru(bpy)<sub>2</sub>(EtOH)<sub>2</sub>]<sup>2+</sup>, formed <em>in situ</em> via Ag<sup>+</sup>-assisted removal of the chlorides from [Ru(bpy)<sub>2</sub>Cl<sub>2</sub>] in ethanolic me&shy;dium, affords a group of pinkish-brown
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Kostryukov, S. G., V. A. Kalyazin, P. S. Petrov, E. V. Bezrukova, and N. V. Somov. "1,3-dipolar cycloaddition as a method for the synthesis of dipyrrolidinyl- and dipyrrolylketones." Журнал общей химии 94, no. 4 (2024): 469–88. http://dx.doi.org/10.31857/s0044460x24040028.

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In the reactions of 1,3-dipolar cycloaddition of a twofold excess of aryl aldimines of glycine ethyl ester with diarylideneacetones and diarylidenecyclohexanones in the presence of silver acetate, the corresponding dipyrrolidinylketones were obtained. Diethyl 4,4′-carbonylbis(3,5-diarylpyrrolidine-2-carboxylates) obtained from diarylideneacetones undergo aromatization under the action of N-bromosuccinimide to form diethyl 4,4′-carbonylbis(3,5-diaryl-1H-pyrrole-2-carboxylates). The selectivity of the reactions and the structure of the products were determined using correlation NMR spectroscopy
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Denmark, Scott, and Hyung Chi. "Synthesis of 2-Alkenyl-Tethered Anilines." Synthesis 49, no. 13 (2017): 2873–88. http://dx.doi.org/10.1055/s-0036-1589002.

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Three general routes for the synthesis of (E)-2-alkenyl-tethered anilines have been developed. The first route involves a 3-aza-Cope rearrangement of N-allylic anilines in the presence of a Lewis acid. The requisite N-allylic anilines were prepared by the addition of vinylmagnesium reagents to the corresponding aldimines. The second route details a direct cross-metathesis of 2-allylic or 2-homoallylic anilines with styrenes. The third route involves a palladium-catalyzed C–N cross-coupling of aryl halides. Taken together, these three strategies allowed access to the requisite aniline substrate
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Li, Yang, Bi-Jie Li, Wen-Hua Wang, et al. "Rhodium-Catalyzed Direct Addition of Aryl CH Bonds to N-Sulfonyl Aldimines." Angewandte Chemie International Edition 50, no. 9 (2011): 2115–19. http://dx.doi.org/10.1002/anie.201007464.

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Li, Yang, Bi-Jie Li, Wen-Hua Wang, et al. "Rhodium-Catalyzed Direct Addition of Aryl CH Bonds to N-Sulfonyl Aldimines." Angewandte Chemie 123, no. 9 (2011): 2163–67. http://dx.doi.org/10.1002/ange.201007464.

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Seth, Dipravath Kumar, and Samaresh Bhattacharya. "Copper(I) complexes of N-(aryl)pyridine-2-aldimines: Spectral, electrochemical and catalytic properties." Polyhedron 30, no. 15 (2011): 2438–43. http://dx.doi.org/10.1016/j.poly.2011.05.037.

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Li, Yang, Bi-Jie Li, Wen-Hua Wang, et al. "ChemInform Abstract: Rhodium-Catalyzed Direct Addition of Aryl C-H Bonds to N-Sulfonyl Aldimines." ChemInform 42, no. 26 (2011): no. http://dx.doi.org/10.1002/chin.201126087.

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Jit, Karmakar, Barua Trisha, Paul Piyali, and Bhattacharya Samaresh. "Interaction of N-(aryl)pyrrole-2-aldimines with Ru(0) : Synthesis, structure and, spectral and electrochemical properties of the resulting complexes." Journal of Indian Chemical Society Vol. 92, Dec 2015 (2015): 1993–99. https://doi.org/10.5281/zenodo.5602564.

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Department of Chemistry, Inorganic Chemistry Section, Jadavpur University, Kolkata-700 032, India <em>E-mail</em> : samaresh_b@hotmail.com Reaction of N-(4&acute;-R-phenyl)pyrrole-2-aldimines (HL-R, where H represents the pyrrole N-H hydrogen and, R = OCH<sub>3</sub> , CH<sub>3</sub> , H and Cl) with [Ru(PPh<sub>3</sub> )<sub>2</sub> (CO)<sub>3</sub> ] in refluxing toluene affords a group of yellow complexes of type [Ru(L-R)(PPh<sub>3</sub> )<sub>2</sub> (CO)(H)], in which the imine-ligand (L-R) is coordinated to the metal center as a mono-anionic bidentate NN-donor along with two triphenylpho
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Zhao, Gui-Ling, and Min Shi. "Baylis–Hillman reactions of N-tosyl aldimines and aryl aldehydes with 3-methylpenta-3,4-dien-2-one." Organic & Biomolecular Chemistry 3, no. 20 (2005): 3686. http://dx.doi.org/10.1039/b510572b.

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Dissertations / Theses on the topic "N-Aryl aldimines"

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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.

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La chimie des ortho-arynes (ou simplement arynes dans la suite de ce manuscrit), c’est-à-dire des arènes contenant formellement une triple liaison dans le cycle aromatique, a connu un regain d'intérêt au cours de la dernière décennie. Les arynes sont des espèces électrophiles très réactives empêchant leur isolement mais permettant leurs réactions avec un grand nombre d'arynophiles. Dans ce manuscrit, nous présentons les tendances actuelles de la chimie des arynes et notre propre travai ldans le domaine. Le but de notre travail était d'explorer l'utilisation de la cycloadditionaza-Diels–Alder e
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