Relevant bibliographies by topics / 1,2,3,4-tetrahydroquinoline

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic '1,2,3,4-tetrahydroquinoline'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "1,2,3,4-tetrahydroquinoline"

1

Möhrle, H., E. Tot, and S. Rüdiger. "1.2.3.4-Tetrahydrochinoline als Substrate für Mannich-Verbindungen / 1.2.3.4-Tetrahydroquinolines as Substrates for Mannich Compounds." Zeitschrift für Naturforschung B 53, no. 7 (1998): 742–52. http://dx.doi.org/10.1515/znb-1998-0715.

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Abstract The product of the reaction of 1,2,3,4-tetrahydroquinoline (1) with 2-naphthol (2) and form aldehyde reported as the N -substituted tetrahydroquinoline 3 show s really the structure of the phenylogous bis-substituted tetrahydroquinoline 4. The function of 1, 6 -methyl-1,2,3,4-tetrahydroquinoline (9) and 1-methyl-1,2 ,3 ,4 -tetrahydroquinoline (17) as amines or C -nucleophilic compounds in Mannich condensations were examined .
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Kafka, Stanislav, Miloslav Ferles, and Miloslav Richter. "Hydroboration of 1-allyl-1,2,3,4-tetrahydroquinoline." Collection of Czechoslovak Chemical Communications 50, no. 5 (1985): 1194–200. http://dx.doi.org/10.1135/cccc19851194.

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Hydroboration of 1-allyl-1,2,3,4-tetrahydroquinoline (I) with triethylamine-borane in the molar ratio 1 : 1 afforded a product from which 6,7-benzo-5-aza-1-boraspiro[4,5]decane (II) was isolated. Ethanolysis of II gave diethyl 3-(1,2,3,4-tetrahydro-1-quinolyl)propylboronate (III). Acid hydrolysis of the crude hydroboration product and subsequent oxidation with alkaline hydrogen peroxide led to a mixture of 3-(1,2,3,4-tetrahydro-1-quinolyl)-1-propanol (IV), 1,2,3,4-tetrahydroquinoline (V) and 1-propyl-1,2,3,4-tetrahydroquinoline (VI). Hydroboration of I with triethylamine-borane in the molar ra
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Gu, Jian-Ming, Xiu-Rong Hu, and Wei-Ming Xu. "7-Nitro-1,2,3,4-tetrahydroquinoline." Acta Crystallographica Section E Structure Reports Online 62, no. 1 (2005): o62—o63. http://dx.doi.org/10.1107/s1600536805040067.

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Ferranti, Anna, Giuseppe Giovanninetti, Francesco Piazza, Patrizia Romualdi, Annalisa Capobianco, and Sanzio Candeletti. "Some new 1,2,3,4-tetrahydroquinoline derivatives." Il Farmaco 55, no. 1 (2000): 47–50. http://dx.doi.org/10.1016/s0014-827x(99)00120-2.

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VOSTRIKOVA, Tatiana V., Vladislav N. KALAEV, Andrey Yu POTAPOV, MICHAIL A. POTAPOV, and Khidmet S. SHIKHALIEV. "USE OF NEW COMPOUNDS OF THE QUINOLINE SERIES AS EFFECTIVE STIMULANTS OF GROWTH PROCESSES." Periódico Tchê Química 17, no. 35 (2020): 781–90. http://dx.doi.org/10.52571/ptq.v17.n35.2020.66_vostrikova_pgs_781_790.pdf.

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The results of a study of the action of compounds of the general formula: 1-alkyl-2,2,4-trimethyl-6-aminocarbothioyl-1,2-dihydroquinoline and 1-alkyl-2,2,4-trimethyl-6-aminocarbothioyl-1,2,3,4-tetrahydroquinoline are presented. The most effective growth stimulants from compounds of the series 1-alkyl-2,2,4-trimethyl-6-aminocarbothioyl-1,2-dihydroquinoline and 1-alkyl-2,2,4-trimethyl-6-aminocarbothioyl-1,2,3,4-tetrahydroquinoline for yellow rhododendron (Rhododendron luteum) and Ledebur rhododendron (Rhododendron ledebourii) were revealed. Rhododendron seedlings were counted to study laboratory
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Šilhánková, Alexandra, Michal Hoskovec, Radek Liboska, and Miloslav Ferles. "Mannich and Grignard reaction of some N-(2-propynyl)azaheterocycles." Collection of Czechoslovak Chemical Communications 54, no. 4 (1989): 1067–81. http://dx.doi.org/10.1135/cccc19891067.

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1,4-Disubstituted butynes IV-VII were prepared by Mannich reaction of N-(2-propynyl) derivatives of 1,2,3,4-tetrahydroquinoline, 1,2,3,4-tetrahydroisoquinoline, piperidine and azacycloheptane with polyoxymethylene and another heterocyclic amines. Reaction of 3-(1-piperidinyl)-1-propynylmagnesium bromide or 3-(1-azacycloheptyl)-1-propynylmagnesium bromide afforded alcohols X-XIII.
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Srinivasan, N., S. Thirumaran, and S. Selvanayagam. "Bis(1,2,3,4-tetrahydroquinoline-1-thiocarbonyl) disulfide." Acta Crystallographica Section E Structure Reports Online 68, no. 12 (2012): o3446. http://dx.doi.org/10.1107/s1600536812047320.

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Zhou, Yong-Gui, Guo-Fang Jiang, and Jie Tang. "Convenient Synthesis of Optically Pure 8-Methoxy-2-methyl-1,2,3,4-tetrahydroquinoline and 2-Methyl-1,2,3,4-tetrahydroquinoline." HETEROCYCLES 82, no. 1 (2010): 887. http://dx.doi.org/10.3987/com-10-s(e)50.

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Luková, Kateřina, Radim Nesvadba, Tereza Uhlíková, et al. "Ab initio conformational analysis of 1,2,3,4-tetrahydroquinoline and the high-resolution rotational spectrum of its lowest energy conformer." Physical Chemistry Chemical Physics 20, no. 21 (2018): 14664–70. http://dx.doi.org/10.1039/c8cp00953h.

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Yan, Xiuli, and Xinzheng Yang. "Mechanistic insights and computational design of half-sandwich iridium and rhodium complexes for hydrogenation of quinoline." New Journal of Chemistry 43, no. 22 (2019): 8459–64. http://dx.doi.org/10.1039/c9nj00835g.

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Dissertations / Theses on the topic "1,2,3,4-tetrahydroquinoline"

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Ngo, Anh Ngoc. "Research in the field of 1,2,3,4-tetrahydroquinoline derivative total synthesis of sumanirole synthetic approach to virantmycin and martinellic acid." Nantes, 2013. https://archive.bu.univ-nantes.fr/pollux/show/show?id=56e15847-aa30-4005-9f62-3513544a999e.

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Depuis quelques années, nous nous intéressons au développement de nouvelles stratégies permettant d’accéder à des structures de type 1,2,3,4-tétrahydroquinoléine en série chirale non-racémique. Au début de cette nouvelle étude, nos observations étaient les suivantes : 1) un composé de Reissert (e. G. 2-cyano-1,2-dihydroquinoléine) peut être préparé, avec une diastéréosélectivité raisonnable (jusque 70%), par action du TMSCN sur un sel de quinoléinium portant une structure de type 4-benzyl-2-oxazilidinone chirale en N1 et 2) une dihydroquinoléine chirale peut être obtenue par une réduction in s
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Juen, Ludovic. "Synthèse et évaluation biologique d'inhibiteurs de STAT5 dans le traitement des leucémies myéloïdes." Thesis, Tours, 2016. http://www.theses.fr/2016TOUR3811/document.

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Les leucémies, syndromes myéloprolifératifs et myelodysplasiques sont la première cause de cancer chez l’enfant de moins de 15 ans. Les facteurs de transcription STAT5 ont un rôle indispensable dans la genèse et le maintien des leucémies. L’inhibition de STAT5 contribuerait à diminuer la survie, l’auto-renouvellement et la quiescence des cellules leucémiques ainsi que leur résistance potentielle aux agents anti-cancéreux. Suite à un précédent criblage de notre chimiothèque, un dérivé comprenant un noyau 4,4-diméthyl-1,2,3,4-tétrahydroquinoléine lié à un indole par une chaine éthoxy, a été iden
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Merriman, Glynn David. "Synthesis of substituted 1,2,3,4-tetrahydroquinolines." Thesis, University of Southampton, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239627.

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Strange, Rosalind H. "Studies towards the synthesis of functionalised 1,2,3,4-tetrahydroisoquinolines." Thesis, University of Bath, 1994. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.760650.

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Luke, Anthony W. "Bis- and Tris-(1,2,3,4-Dithiadiazolium) salts and related radicals." Thesis, Durham University, 1992. http://etheses.dur.ac.uk/5724/.

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Using the cycloaddition of [SNS][AsF(_6)] to nitriles a variety of 5-substituted-1,3,2,4- dithiadiazolium salts (salts containing the -CNSNS cationic ring) were prepared : mono- (1,3,2,4-dithiadiazolium) salts from mononitriles, bis-(l,3,2,4-dithiadiazolium) salts from dinitriles and l,3,5-tris-(l,3,2,4-dithiadiazohum) salts from 1,3,5-tricyanobenzene. salts of these dithiadiazolium cations with other anions were prepared by simple anion metathesis reactions. Bis- and tris-(l,3,2,4-dithiadiazolium) salts were reduced to give stable bis- and tris- (1,3,2,4-dithiadiazolyl) radicals which were st
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Strike, David Jonathan. "Electrocatalytic oxidation of reduced cofactors by oxidised 1,2,3,4-tetrahydroquinoxalines." Thesis, University of Cambridge, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358813.

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Jones, Michael William Chemistry Faculty of Science UNSW. "Enhancing the cooperative binding properties of 1,1'-bis(1,2,3,4-tetrahydroisoquinolines)." Awarded by:University of New South Wales. School of Chemistry, 2005. http://handle.unsw.edu.au/1959.4/27400.

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The design of partially reduced 1,1'-bisisoquinoline derivatives was investigated with the aim of controlling the conformation about the C1-C1' axis. This would produce ligands with unusual but predictable ligand binding properties, particularly cooperativity. The introduction of ??-aminoalkyl, ??-azidoalkyl, ??-alkynyl and ??-alkenyl groups onto the nitrogens of the reduced bisisoquinoline core was conducted with the intention of broadening the scope of the ligand. Subsequent epoxidation, hydroboration and Huisgen 1,3-dipolar cycloaddition of terminal unsaturated groups and nucleophilic displ
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張文驥 and Man-ki Cheung. "Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1995. http://hub.hku.hk/bib/B31234148.

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O'Callaghan, John Mark. "The synthesis and reactions of some polysubstituted 1,2,3,4-tetrahydroisoquinolinetricarbonylchromium adducts." Thesis, Open University, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.232899.

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Cheung, Man-ki. "Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole /." [Hong Kong] : University of Hong Kong, 1995. http://sunzi.lib.hku.hk/hkuto/record.jsp?B14786898.

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Books on the topic "1,2,3,4-tetrahydroquinoline"

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Gursky, Andreas. Untitled XII: No. 1,2,3,4. Matthew Marks Gallery, 2001.

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1,2,3,4 double-ended hook crochet. DRG, 2010.

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Morris, Robert M. Clymu'r canrifoedd: Cyfnodau Allweddol 1,2,3,4. Y Ganolfan Adnoddau Addysg, 1993.

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Brunel University. Department of Production Technology. Exam papers: BSc, Years 1,2,3,4, 1986. Brunel University, 1986.

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Negara, Perusahaan Listrik. Studi evaluasi lingkungan PLTU Belawan unit 1,2,3,4 dan pengembangan PLTG/U blok 1+2: Laporan utama. Perusahaan Umum Listrik Negara, 1993.

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Skinner, V. L. Abstracts of the proceedings of the Orphans' Court of Sussex County, Delaware: Libers 1,2,3,4, A, 1708-1709, 1728-1777. Willow Bend Books, 2000.

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Loblolly Numbers 1,2,3,4. Lv Boling Books, 1986.

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Grant, Morrison. Fantastic Four: 1,2,3,4 HC. Marvel Comics, 2007.

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Autoren, Verschiedene. 1,2,3,4 ... Massenmoerder Unter Sich. Intrag Int'l, 2006.

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Johnstone, William, I. McCafferty, and J. D. Martin. Computerized Introductory Hebrew Grammer: Full Sound, Disk 1,2,3,4. T. & T. Clark Publishers, 1999.

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Book chapters on the topic "1,2,3,4-tetrahydroquinoline"

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Wystrach, V. P. "The 1,2,3,4-Tetrazines." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186589.ch3.

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Demaison, J. "513 C5H2 1,2,3,4-Pentatetraenylidene." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_261.

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Wohlfarth, Ch. "Viscosity of 1,2,3,4-tetrahydronaphthalene." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_336.

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Wohlfarth, Christian. "Viscosity of 1,2,3,4-tetrahydronaphthalene." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_335.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "49 C6H2F4 1,2,3,4-Tetrafluorobenzene." In Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_180.

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Bährle-Rapp, Marina. "1,2,3,4-Tetrahydro-6-Nitroquinoxaline." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10462.

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Wohlfarth, Ch. "Refractive index of 1,2,3,4-tetrahydronaphthalene." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38). Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_300.

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Wohlfarth, Ch. "Dielectric constant of 1,2,3,4-tetrahydronaphthalene." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_289.

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Wohlfarth, Christian. "Refractive index of 1,2,3,4-tetrahydronaphthalene." In Optical Constants. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49236-9_351.

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Demaison, J. "517 C5H2S 1,2,3,4-Pentatetraen-1-thione." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_265.

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Conference papers on the topic "1,2,3,4-tetrahydroquinoline"

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Corporan, Edwin, and Donald K. Minus. "Hydrogen Donors: Thermal Stabilizers for JP-8+100 at High Temperatures." In ASME 1999 International Gas Turbine and Aeroengine Congress and Exhibition. American Society of Mechanical Engineers, 1999. http://dx.doi.org/10.1115/99-gt-056.

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The effectiveness of hydrogen donor compounds as additives to reduce pyrolytic deposition in JP-8+100 at high temperatures was assessed. Decalin and 1,2,3,4 tetrahydroquinoline (THQ) were added to JP-8+100 at 0.5% (decalin only), 1.0 and 2.5% w/w concentrations and tested in a flow reactor at a fuel exit temperature of 600°C at 5.2 MPa. Measurements of carbon deposits along the tube and gas chromatography/mass spectrometry (GC/MS) analysis of the stressed and unstressed liquid fuel were used to assess effectiveness of the additive, and the degree of fuel decomposition. Additionally, liquid-to-
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Dalinger, Igor. "MESOIONIC 1,2,3,4-OXATRIAZOLES: SYNTHESIS AND PROPERTIES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m736.aks-2019/126-128.

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Rogozin, Mark, Konstantin Pekhotin, Oksana Golubtsova, Rudolf Stepanov, Ludmila Kruglyakova, and Alexander Vasiliev. "Synthesis of 2-nitromethyl-5-nitro-1,2,3,4-tetrazole." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01877.

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Redda, Kinfe Ken, Madhavi NA Gangapuram, and Tiffany W. Ardley. "Abstract 735: Synthesis of substituted 1,2,3,4-tetrahydroisoquinolines as anticancer agents." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-735.

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Litwin, Wojciech, and Artur Olszewski. "Properties Comparison of Two Water Lubricated Rubber Bearings Based on Experimental Test." In ASME/STLE 2012 International Joint Tribology Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/ijtc2012-61106.

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Water lubricated rubber bearings are used from many years in ship building and other industry because of their advantages such as: long serviceable life, low coefficient of friction, long life of shaft sleeve, good vibration damping, good abrasion resistance, low maintenance required, grit particles and other abrasives are expelled through the grooves [1,2,3,4].
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Sanmartín-Matalobos, Jesús, Lucía Briones-Miguéns, Cristina Portela-García, Ana García-Deibe, Matilde Fondo, and Concepcion González-Bello. "Copper-mediated aerobic synthesis of 3-tosyl-1,2,3,4-tetrahydroquinazoline from 2 tosylaminomethylaniline and methanol." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a003.

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Stratan, Aurel, Alexandru Zorila, Laurentiu Rusen, et al. "Automated test station for laser-induced damage threshold measurements according to ISO 21254-1,2,3,4 standards." In SPIE Laser Damage, edited by Gregory J. Exarhos, Vitaly E. Gruzdev, Joseph A. Menapace, Detlev Ristau, and M. J. Soileau. SPIE, 2012. http://dx.doi.org/10.1117/12.976845.

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Kaşıkcı, Tuğçe, Ming-Chih Weng, Ash Nayak, Turguy Goker, and Sinan Müftü. "Tape Mechanics Over a Grooved Roller: Experiments and Theory." In ASME 2014 Conference on Information Storage and Processing Systems. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/isps2014-6968.

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In the case of an axially translating tape, supported by a roller, the effects of air entrainment can be reduced by a grooved roller. Use of grooves on the roller surface substantially improves the traction capacity, relative to a non-grooved roller surface [1,2,3,4]. In our previous work, a mechanics model of the tape interacting with a grooved roller was presented [5]. In this work, a comparison of the experimental and modeling studies of the tape-to-grooved-roller spacing is reported.
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Savu, Lucian, Aurel Abalaru, Daniela Cioboata, Danut Stanciu, and Cristian Logofatu. "Intelligent mechatronic equipment for shock and axes distance control of free gears 1,2,3,4 and primary shaft." In 2011 IEEE International Conference on Mechatronics (ICM). IEEE, 2011. http://dx.doi.org/10.1109/icmech.2011.5971247.

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Gámez-Montaño, Rocío, Manuel A. Rentería-Gómez, and Alejandro Islas-Jácome. "Synthesis of 1-tetrazolyl-1,2,3,4-tetrahydroisoquinoline bound-type bis-heterocycles via oxidative Ugi-azide reaction." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a030.

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Reports on the topic "1,2,3,4-tetrahydroquinoline"

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Steele, W., S. Knipmeyer, and R. Chirico. Critical property and high-temperature heat-capacity measurements on quinoline and 5,6,7,8-tetrahydroquinoline. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6957875.

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Steele, M. V., R. D. Chirico, I. A. Hossenlopp, and N. K. Smith. The thermodynamic properties of 1,2,3,4- and 5,6,7,8-tetrahydroquinolines: Topical report. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/6433416.

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Steele, W. V., S. E. Knipmeyer, A. Nguyen, and R. D. Chirico. Thermodynamic properties of 9-methylcarbazole and 1,2,3,4-tetrahydro-9-methylcarbazole. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/5689959.

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Beaver, Bruce. Iron (III) Initiated Autoxidation of 1,2,3,4- Tetrahydrocarbazole: An Example of Electron Transfer. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada211857.

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Shechter, H., M. Venugopal, and D. Srinivasulu. Syntheses of 1,2,3,4-Tetrazine Di-N-oxides, Pentazole Derivatives, Pentazine Poly-N-oxides, and Nitroacetylenes. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada445136.

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Roots, C. Geological map of southern Mayo map area (105M/1,2,3,4 and parts of 105M/5 and 6), Yukon. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1995. http://dx.doi.org/10.4095/203618.

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Hazen, T. C. Operations Support of Phase 2 Integrated Demonstration In Situ Bioremediation. Volume 3, Final report: Data in graphical form, Disks 1,2,3,4; Averaged data in tabular form, Disks 1,2. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10161897.

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Hazen, T. C. Operations Support of Phase 2 Integrated Demonstration In Situ Bioremediation. Volume 4, Final report: Averaged data in tabular form, Disks 3,4; Averaged data in graphical form, Disks 1,2,3,4. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10161901.

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