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Books on the topic 'Quinolium'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Rutherford, Mary Jean. Dimeric indole and quinoline alkaloids. The author], 1985.

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2

Neville, Charles Frederick. The synthesis and biosynthesis of quinoline alkaloids. The Author], 1989.

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3

Greer, Robert James. Studies in the synthesis of quinoline alkaloids. The Author), 1987.

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4

Giles, Janice S. In vitro efficacy of six antibiotics and plasma concentrations of two quinolines in Atlantic salmon (salmon salari). University of Prince Edward Island, 1992.

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5

Giles, Janice S. In vitro efficacy of six antibiotics and plasma concentrations of two quinolines in Atlantic salmon (salmon salari). National Library of Canada, 1992.

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6

Edlund, Charlotta. Ecological aspects of new quinolones: Impact on human oropharyngeal and gastrointestinal microflora. Kongl. Karolinska Medico Chirurgiska Institutet, 1989.

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7

Ronne, Erik. Synthesis of imidazoazaarenes. Swedish University of Agricultural Sciences, Dept. of Chemistry, 1994.

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8

Jones, Dewitt Owen. Catalysis of Hydrogen Peroxide in Quinoline Solutions. Creative Media Partners, LLC, 2023.

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9

Di, Kaiying. Interactions between substrates and starved subsurface bacteria in a dual-bacteria/dual-contaminant system. 1993.

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10

Zhang, Jinying. Effects of quinolinate and nitro-, or thio- substituted analogs of quinolinate on glutamate recepter-mediated neurotoxicity in cerebellar granule cell cultures. 1998.

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11

Mahiou, Belaid. Atom abstraction from excoyclic postitons of derivatives of methylated pyridines and quinolines: An evaluation of change separation in the transition states of these reactions. 1989.

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12

Erickson, W. Randal. Studies on advanced intermediates in the biosynthesis of streptonigrin. 1987.

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13

Hewitt, J. T. Synthetic Colouring Matters Dyestuffs Derived from Pyridine, Quinoline, Acridine and Xanthene. Creative Media Partners, LLC, 2022.

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14

Hewitt, J. T. Synthetic Colouring Matters Dyestuffs Derived from Pyridine, Quinoline, Acridine and Xanthene. Creative Media Partners, LLC, 2022.

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15

Dauble, Dennis D. Mechanisms affecting the bioaccumulation of dietary quinoline by rainbow trout (Salmo gairdneri). 1988.

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16

Hewitt, John Theodore. Synthetic Coloring Matters: Dyestuffs Derived From Pyridine, Quinoline, Acridine And Xanthene (1922). Kessinger Publishing, LLC, 2010.

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17

Eland, John H. D., and Raimund Feifel. Conjugated and aromatic molecules. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198788980.003.0006.

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In the vast majority of conjugated and aromatic molecules, the outermost occupied orbitals are either of π‎ character or non-bonding lone pairs belonging to heteroatoms. These are the orbitals from which double ionisation gives rise to most of the distinct bands that can be discerned in their spectra. Double photoionisation spectra of ethylene, butadiene, pyrrole, furan, thiophene, benzene, hexafluorobenzene, toluene, pyridine, pyrazine, pyrimidine, pyridazine, naphthalene, azulene, quinoline, biphenyl, TDME, iron pentacarbonyl, ferrocene, and TMPPD are presented with analysis where possible.

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18

Truex, Michael J. Effect of starvation on the induction of quinoline degradation for a ground water bacterium in a continuous-flow column. 1991.

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19

Singh, Rajesh Kumar, ed. Key Heterocyclic Cores for Smart Anticancer Drug–Design Part I. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/97898150400741220101.

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This book provides an update on heterocyclic compounds that serve as key components of anti-cancer agents administered in pre-clinical settings. Many of the compounds highlighted in the book are being actively investigated for the bioactive properties against a range of cancer cell lines. There is potential for heterocyclic compounds to design agents that can target specific molecules to treat different types of cancers. Chapters are contributed by experts in pharmaceutical chemistry and are written to give a general overview of the topic to readers involved in all levels of research and decis

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20

Parker, Philip M. The 2007 Import and Export Market for Heterocyclic Compounds with Nitrogen Hetero-Atom(s) Only, Containing a Quinoline or Isoquinoline Ring-System Not Further Fused in China. ICON Group International, Inc., 2006.

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21

The World Market for Heterocyclic Compounds with Nitrogen Hetero-Atom(s) Only, Containing a Quinoline or Isoquinoline Ring-System Not Further Fused: A 2004 Global Trade Perspective. Icon Group International, Inc., 2005.

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22

Parker, Philip M. The World Market for Heterocyclic Compounds with Nitrogen Hetero-Atom(s) Only, Containing a Quinoline or Isoquinoline Ring-System Not Further Fused: A 2007 Global Trade Perspective. ICON Group International, Inc., 2006.

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23

Parker, Philip M. The 2007 Import and Export Market for Heterocyclic Compounds with Nitrogen Hetero-Atom(s) Only, Containing a Quinoline or Isoquinoline Ring-System Not Further Fused in India. ICON Group International, Inc., 2006.

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24

Parker, Philip M. The 2007 Import and Export Market for Heterocyclic Compounds with Nitrogen Hetero-Atom(s) Only, Containing a Quinoline or Isoquinoline Ring-System Not Further Fused in United States. ICON Group International, Inc., 2006.

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