Relevant bibliographies by topics / Quinolizines

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

Academic literature on the topic 'Quinolizines'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Quinolizines"

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Gootjes, J., A. M. de Roos, and W. Th Nauta. "Derivatives of benzo- and indolo-quinolizines. III: The stereochemistry of 2-substituted hexahydro-2H-benzo[a]quinolizines and octahydroindolo[2,3-a]quinolizines." Recueil des Travaux Chimiques des Pays-Bas 85, no. 5 (2010): 491–503. http://dx.doi.org/10.1002/recl.19660850510.

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Zhao, Ming, Min Guo, Chao Wang, Shiqi Peng, and Ekkehard Winterfeld. "Synthesis of enantiopure oxoindolo-quinolizines." Journal für praktische Chemie 341, no. 7 (1999): 677–84. http://dx.doi.org/10.1002/(sici)1521-3897(199910)341:7<677::aid-prac677>3.0.co;2-h.

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Chen, Li, Rong Huang, Kun Li, Xing-Han Yun, Chang-Long Yang, and Sheng-Jiao Yan. "An environmentally benign cascade reaction of chromone-3-carboxaldehydes with ethyl 2-(pyridine-2-yl)acetate derivatives for highly site-selective synthesis of quinolizines and quinolizinium salts in water." Green Chemistry 22, no. 20 (2020): 6943–53. http://dx.doi.org/10.1039/d0gc02460k.

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Gootjes, J., and W. Th Nauta. "Derivatives of benzo- and indolo-quinolizines II. Synthesis of 2-substituted hexahydro-2h-benzo[a]quinolizines and octahydroindolo[2,3-a]quinolizines from substituted valerolactones." Recueil des Travaux Chimiques des Pays-Bas 84, no. 11 (2010): 1427–41. http://dx.doi.org/10.1002/recl.19650841107.

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Gootjes, J., and W. Th Nauta. "Derivatives of benzo- and indolo-quinolizines IV: Synthesis of some 1- or 3-substituted hexahydro-2H-benzo[a]-quinolizines and octahydroindolo[2,3-a]quinolizines." Recueil des Travaux Chimiques des Pays-Bas 85, no. 9 (2010): 966–72. http://dx.doi.org/10.1002/recl.19660850913.

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Ram, Vishnu Ji. "Synthesis of Quinolizines, Pyrano[4,3-b]quinolizines and Azaquinolizines Through Nucleophile Induced Ring Transformation Reactions." Synthesis 1999, no. 11 (1999): 1884–88. http://dx.doi.org/10.1055/s-1999-3605.

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Gootjes, J., and W. Th Nauta. "Derivatives of benzo- and indolo-quinolizines: I Synthesis of 2-substituted hexahydro-2H-benzo[a]quinolizines and octahydroindolo[2,3-a]quinolizines from substituted glutaric acids." Recueil des Travaux Chimiques des Pays-Bas 84, no. 9 (2010): 1183–99. http://dx.doi.org/10.1002/recl.19650840911.

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Ram, Vishnu Ji, Pratibha Srivastava, M. Nath, and Abhishek S. Saxena. "ChemInform Abstract: Synthesis of Quinolizines, Pyrano[4,3-b]quinolizines and Azaquinolizines Through Nucleophile Induced Ring Transformation Reactions." ChemInform 31, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.200008167.

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Zhao, Ming, Chao Wang, Min Guo, Shiqi Peng, and Ekkehard Winterfeldt. "ChemInform Abstract: Synthesis of Enantiopure Oxoindolo-quinolizines." ChemInform 31, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.200004170.

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Volovenko, Yu M., and E. V. Blyumin. "Unexpected formation of pyrimido[4,5-c]quinolizines." Chemistry of Heterocyclic Compounds 34, no. 12 (1998): 1442–43. http://dx.doi.org/10.1007/bf02317818.

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Dissertations / Theses on the topic "Quinolizines"

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Eschenbrenner-Lux, Vincent [Verfasser], Herbert [Akademischer Betreuer] Waldmann, and Frank [Gutachter] Schulz. "Development of cascade reactions to ring fused quinolizines for the synthesis of a natural product inspired compound collection / Vincent Eschenbrenner-Lux. Betreuer: Herbert Waldmann. Gutachter: Frank Schulz." Dortmund : Universitätsbibliothek Dortmund, 2014. http://d-nb.info/1107197309/34.

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LE, GOFF-BEVIERE CORINNE. "Pharmacomodulations de quinolones a structure benzo-ij-quinolizine : synthese et activite antibacterienne." Orléans, 1995. http://www.theses.fr/1995ORLE2019.

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L'objectif principal de notre travail sur la pharmacomodulation de quinolones nous a amenes a mettre au point de nouvelles strategies de synthese dans le domaine des quinoleines, a partir d'un synthon unique, la 6-fluoro-2-methylquinoleine conduisant aux precurseurs necessaires a la realisation des quinolones a structure benzoi,jquinolizine. Ainsi, l'utilisation des tetrahydroquinoleines-n-formylees nous a permis par des fonctionnalisations regioselectives d'atteindre des pharmacomodulations donnant acces aux heterocycles imidazo, thiazolo et oxazolo en position 4,5-g sur le noyau quinoleique.
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Memetzidis, Georgios. "Pharmacochimie de la tetrahydro-5,6,13,13a 8h-dibenzo (a, g) quinolizine ou berbine." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13159.

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Liu, Yannan. "Benzo[c]quinolizine, coumarin, and spiroisoxazolinoproline : lead-based heterocycle design and parallel synthesis /." For electronic version search Digital dissertations database. Restricted to UC campuses. Access is free to UC campus dissertations, 2002. http://uclibs.org/PID/11984.

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Semak, Vladislav. "Synthesis of 1S-ethyl-4-substituted quinolizidines and other potentially bioactive compounds." Doctoral thesis, Universitat de Barcelona, 2012. http://hdl.handle.net/10803/97241.

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Esta Tesis Doctoral se presenta como Compendio de publicaciones. Los capítulos en los que se ha dividido la presente Tesis son los siguientes: Capítulo 1 – parte A: Enantioselective, Protecting Group-Free Synthesis of 1S-Ethyl-4-Substituted Quinolizidines Se ha descrito una síntesis enantioselectiva que no implica grupos protectores para acceder a la quinolizidina clave 6 a partir de la lactama bicíclica derivada de fenilglicinol 1. La adición de un reactivo organometálico a 6 ocurre de manera estereoselectiva para conducir a las quinolizidinas 1S-etil-4-sustituidas 4-epi-207I y 7-9. Sigu
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Memetzidis, Georgios. "Pharmacochimie de la tétrahydro-5, 6, 13, 13a 8H-dibenzo [a, g] quinolizine ou berbine." Grenoble 2 : ANRT, 1988. http://catalogue.bnf.fr/ark:/12148/cb37616245j.

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MONTHILLER, SOPHIE. "Synthese de 9-oxa-quinolizidines, inhibiteurs potentiels de glycosidases a visee anti-vih." Université Louis Pasteur (Strasbourg) (1971-2008), 1994. http://www.theses.fr/1994STR13138.

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Ce travail traite de la synthese et de l'evaluation biologique de 9-oxaquinolizidines, inhibiteurs potentiels de glycosidases a visee anti-sida. La conception de ces nouveaux inhibiteurs de glycosidases possedant une fonction perhydro-oxazine, a ete realisee en se basant sur le mecanisme d'hydrolyse des glycosides. Le principe des syntheses repose sur l'utilisation d'hexopyranoses comme produit de depart, de meme stereochimie que les composes souhaites. Cette derniere a ete conservee via des reactions d'amination reductrice stereoselectives. Les reactivites observees en serie glucose, mannose
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Murphy, Elliot Anthony. "Very strongly σ-donating carbenes and pseudo-amides based on benzo[c]quinolizine : synthesis, properties and use as ligands". Thesis, University of Bristol, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.653076.

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Following DFT calculations, the structure of a new, remotely stabilised, N-heterocyclic carbene, thought to be very strongly a-donating, was proposed. This structure was benzo[c]quinolizin-6-ylidene. Synthesis of the basic scaffold of the benzo[c]quinolizine ring system was performed, giving benzo[c]quinolizin-6-one (2.3a). Several novel 5 and 7 substituted varieties (2.3b-e) were also synthesised, requiring the development of a new route, due to the failure of the initial coupling step when using substituted substrates.
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Maloney, Kevin M. (Kevin Matthew). "[4+2] cycloadditions of iminoacetonitriles : a general strategy for the synthesis of quinolizidines, indolizidines, and piperidines." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/39739.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2007.<br>Vita.<br>Includes bibliographical references.<br>Iminoacetonitriles participate as reactive dienophiles in intermolecular and intramolecular Diels-Alder cycloadditions leading to quinolizidines, indolizidines, and piperidines. The resultant a-amino nitrile cycloadducts are versatile synthetic intermediates which can be further elaborated by stereoselective alkylation, reduction, reductive cyclization, and Bruylants reactions. The first part of this thesis describes the full details of our studies on the synthe
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Evano, Gwilherm. "Nouvelles utilisations de beta-aminoalcools pour la synthèse d'hétérocycles azotés." Paris 6, 2002. http://www.theses.fr/2002PA066128.

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Book chapters on the topic "Quinolizines"

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Shipman, M. "Ring Contraction of 4-Quinolizines." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-01036.

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Tominaga, Y. "[3.3.3]Cyclazines (Pyrido[2,1,6-]quinolizines) and Related Compounds." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01701.

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Tominaga, Y. "[2.3.3]Cyclazines (Pyrrolo[2,1,5-]quinolizines) and Related Compounds." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01661.

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Garnett, Ian. "The quinolizine alkaloids." In Second Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds. Elsevier, 1991. http://dx.doi.org/10.1016/b978-044453347-0.50207-x.

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Hartmann, Thomas. "Quinolizidines and Pyrrolizidines." In Phytochemicals in Plant Cell Cultures. Elsevier, 1988. http://dx.doi.org/10.1016/b978-0-12-715005-5.50023-6.

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Tominaga, Y. "[3.3.3]Cyclazine (Pyrido[2,1,6-]quinolizine)." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01702.

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Ihmels, H. "Of 2-Quinolizin-2-one." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01560.

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Ihmels, H. "Of 6-Benzo[]quinolizine-6-carbonitrile Derivatives." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01593.

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Tominaga, Y. "Reaction of Cyclopenta[]quinolizine with Dimethyl Acetylenedicarboxylate." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01706.

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Tominaga, Y. "Thermolysis of a Pyrido[2,1,6-]quinolizine-4,5-dicarboxylate." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-01714.

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Conference papers on the topic "Quinolizines"

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Cely-Veloza, W., and E. Coy-Barrera. "Identification of antifungal quinolizidines using GC/MS-based metabolomics." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399830.

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Gonçalves, M. Sameiro, Maria Inês Leitão, B. Rama Raju, and Maria João Sousa. "Antiproliferative Activity of 2,3,6,7-Tetrahydro-1H-Benzo[a]Quinolizino[1,9-hi]Phenoxazin-14(5H)-Iminium Chloride Derivatives." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-b027.

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