Relevant bibliographies by topics / Arylalkyl

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Arylalkyl'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Arylalkyl"

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Rzadkowska, Marzena, Elzbieta Szacon, and Maria Zun. "Synthesis of new derivatives of 9-(2-pyridyl)-3-aryl(arylalkyl)- -2,4,5(9H)trioxo-7,8-dihydroimidazo[1,2-a][1,3,5]triazepine." Current Issues in Pharmacy and Medical Sciences 27, no. 1 (2014): 8–9. http://dx.doi.org/10.2478/cipms-2014-0002.

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Abstract A series of new derivatives of 9-(2-pyridyl)-3-aryl(arylalkyl)-2,4,5(9H)trioxo-7,8- dihydroimidazo [1,2-a][1,3,5] triazepine was obtained by condensation of 1-[1-(2-pyridyl) imidazolidine-2-ylidene]-3-aryl(arylalkyl)ureas) with diethyl oxalic acid ester. Considering the structure of the obtained compounds, it can be expected that these compounds can reveal pharmacological activity.
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Liu, Ming-Qing, Tao Jiang, Wen-Wen Chen, and Ming-Hua Xu. "Highly enantioselective Rh/chiral sulfur-olefin-catalyzed arylation of alkyl-substituted non-benzofused cyclic N-sulfonyl ketimines." Organic Chemistry Frontiers 4, no. 11 (2017): 2159–62. http://dx.doi.org/10.1039/c7qo00555e.

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Wang, Zheng, Jinjin Ye, Rui Wu, et al. "Bi-aryl rotation in phenyl-dihydroimidazoquinoline catalysts for kinetic resolution of arylalkyl carbinols." Catal. Sci. Technol. 4, no. 7 (2014): 1909–13. http://dx.doi.org/10.1039/c3cy00904a.

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Chiral nucleophilic catalysts, 6-aryl-phenyl-dihydroimidazoquinolines (PIQs), were designed, synthesised and applied to the kinetic resolution of arylalkyl carbinols with very high selectivity (S) factors (up to 530).
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Abidin, Mohammad Z., Thangavelu Saravanan, Laura Bothof, Pieter G. Tepper, Andy-Mark W. H. Thunnissen, and Gerrit J. Poelarends. "Biocatalytic enantioselective hydroaminations enabling synthesis of N-arylalkyl-substituted l-aspartic acids." Organic & Biomolecular Chemistry 19, no. 29 (2021): 6407–11. http://dx.doi.org/10.1039/d1ob00748c.

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EDDS lyase has a broad substrate scope, accepting diverse arylalkylamines in the enantioselective hydroamination of fumarate enabling the facile synthesis of difficult N-arylalkyl-substituted l-aspartic acids with excellent optical purity.
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AQUINO, M., S. CARDANI, G. FRONZA, C. FUGANTI, R. P. FERNANDEZ та A. TAGLIANI. "ChemInform Abstract: Baker′s Yeast Reduction of Arylalkyl and Arylalkenyl γ- and . delta.-Keto Acids." ChemInform 23, № 2 (2010): no. http://dx.doi.org/10.1002/chin.199202079.

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Zhigang, Xu, Zhao Yu, Yuan Bing, Qiao Weihong, Li Zongshi, and Cheng Lubo. "Synthesis of Novel Arylalkyl Sulfonate Surfactants." Tenside Surfactants Detergents 41, no. 1 (2004): 31–33. http://dx.doi.org/10.3139/113.100206.

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Azzena, Ugo, Simonetta Carta, Giovanni Melloni, and Alessandra Sechi. "Reductive lithiation of arylalkyl methyl ethers." Tetrahedron 53, no. 47 (1997): 16205–12. http://dx.doi.org/10.1016/s0040-4020(97)10080-1.

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deSolms, S. Jane, Elizabeth A. Giuliani, Samuel L. Graham, et al. "N-Arylalkyl Pseudopeptide Inhibitors of Farnesyltransferase." Journal of Medicinal Chemistry 41, no. 14 (1998): 2651–56. http://dx.doi.org/10.1021/jm9800907.

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Watanabe, S., Y. Igarashi, and K. Yagami. "Antimicrobial activity of someN-(arylalkyl)maleimides." Pesticide Science 34, no. 2 (1992): 99–104. http://dx.doi.org/10.1002/ps.2780340202.

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Kniphorst, L. C. E. "The nitration of symmetrical arylalkyl-ureas." Recueil des Travaux Chimiques des Pays-Bas 44, no. 8 (2010): 693–727. http://dx.doi.org/10.1002/recl.19250440806.

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Dissertations / Theses on the topic "Arylalkyl"

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Quandt, Gabriele [Verfasser]. "Synthese von GABA-Uptake-Inhibitoren mit fluorsubstituierten N-Arylalkyl-Einheiten sowie photoschaltbaren Resten / Gabriele Quandt." München : Verlag Dr. Hut, 2013. http://d-nb.info/1042878285/34.

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Lutz, Toni Alexander [Verfasser]. "Syntheses of nipecotic acid derivatives with new N-arylalkenyl and N-arylalkynyl substituents and new photoswitchable residues as mGAT1 inhibitors / Toni Alexander Lutz." München : Verlag Dr. Hut, 2018. http://d-nb.info/1161250875/34.

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Lutz, Toni Alexander [Verfasser], and Klaus T. [Akademischer Betreuer] Wanner. "Syntheses of nipecotic acid derivatives with new N-arylalkenyl and N-arylalkynyl substituents and with new photoswitchable residues as mGAT1 inhibitors / Toni Alexander Lutz ; Betreuer: Klaus T. Wanner." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2017. http://d-nb.info/1160875812/34.

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Maluleka, Marole Maria. "Synthesis, biological evaluation and molecular docking studies of novel indole- and benzofuran-chalcone and benzofuran-quinazoline hybrids as anticancer agents." Thesis, 2019. http://hdl.handle.net/10500/25821.

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Text in English<br>Specially prepared 2-amino-5-bromo-3-iodoacetophenone and 5-bromo-2-hydroxy-3 iodoacetophenone were subjected to Claisen-Schmidt aldol condensation with benzaldehyde derivatives followed by sequential and/or one-pot palladium catalyzed Sonogashira cross coupling and heteroannulation of the 3-alkynylated intermediates to afford indole-chalcones and benzofuran-chalcones, respectively. The indole-chalcones derivatives were, in turn, subjected to trifluoroacetic anhydride in tetrahydrofuran under reflux to afford the corresponding 3-trifluoroacetyl substituted indole-chalcone d
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Book chapters on the topic "Arylalkyl"

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Henrie, Robert N., Syed F. Ali, Katherine G. Anouna, et al. "InsecticidalN-Arylalkyl-4-benzhydrolpiperidines: Optimization of the Benzhydrol Region." In ACS Symposium Series. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2002-0800.ch020.

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lvarez, M., and J. A. Joule. "From 2,2-Dialkoxy--(1-arylalkyl)--(benzylsulfonyl)ethylamines." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01231.

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lvarez, M., and J. A. Joule. "From 2,2-Dialkoxy--(1-Arylalkyl)ethylamines Using Chlorosulfonic Acid." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01229.

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Sainsbury, Malcolm. "Aromatic compounds." In Aromatic Chemistry. Oxford University Press, 1992. http://dx.doi.org/10.1093/hesc/9780198556749.003.0006.

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This chapter assesses aromatic compounds. Alkenylbenzenes are normally synthesized through the dehydration of arylalkanols, or by the dehydrohalogenation of arylalkyl halides. The best known alkenylarene, ethenylbenzene (styrene), is obtained commercially from benzene in two steps: first, alkylation with ethene in the presence of an acid or a Lewis acid, and second, dehydrogenation of the product, ethylbenzene, by heating over a catalyst at 600°C. Styrene undergoes radical initiated polymerization with itself, to form polystyrene, or with other molecules to form copolymers; both processes have
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Olah, George A., Leslie D. Field, Koop Lammertsma, Donald Pacquin, and Klaus Suemmerman. "THE REACTION OF SILANE, ARYL, ALKYL, AND ARYLALKYL SILANES WITH DIBORANE." In World Scientific Series in 20th Century Chemistry. World Scientific Publishing Company, 2003. http://dx.doi.org/10.1142/9789812791405_0227.

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"1-(Hydrogen-, alkyl-, aryl-, heterocyclyl-, arylalkyl-, heterocyclylalkyl-, diphenylalkyl- and trityl)1-H-azoles." In Antifungal Azoles. Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527602682.ch2.

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lvarez, M., and J. A. Joule. "From 1-Arylalkan-1-imines." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01172.

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Murphy, P. J. "From 1-Arylalk-1-ynes." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00481.

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Aitken, R. A. "10.18 Benzo[c]phospholes." In Knowledge Updates 2022/2. Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/sos-sd-110-02186.

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AbstractThis chapter is a complete revision and update of the earlier Science of Synthesis contribution from 2000 describing methods for the synthesis of benzo[c]phospholes. A third of the references describe newer methods reported between 2000 and 2021 and several completely new approaches are included. Synthetic strategies for preparing these ring systems include metal-mediated reactions of 2,2′-bis(arylalkynyl)biaryls with phosphorus dihalides, reaction of ortho-disubstituted benzenes with phosphorus compounds, and aromatization of dihydrobenzo[c]phospholes.
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Joule, J. A. "From 2-Arylalkenyl Azides; Hemetsberger–Knittel Synthesis." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00605.

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Conference papers on the topic "Arylalkyl"

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Glimsdal, Eirik, Marcus Carlsson, Bertil Eliasson, Robert Westlund, and Mikael Lindgren. "Photo-physical properties and OPL of some new longer thiophenyl-containing arylalkynyl Pt(II) compounds." In Optics/Photonics in Security and Defence, edited by James G. Grote, Francois Kajzar, and Mikael Lindgren. SPIE, 2007. http://dx.doi.org/10.1117/12.737696.

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Journal articles
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