Relevant bibliographies by topics / Acylhydrazone pyridine

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Acylhydrazone pyridine'

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

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Journal articles on the topic "Acylhydrazone pyridine"

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Nogueira, Thais Cristina Mendonça, Lucas dos Santos Cruz, Maria Cristina Lourenço, and Marcus Vinicius Nora de Souza. "Design, Synthesis and Anti-tuberculosis Activity of Hydrazones and N-acylhydrazones Containing Vitamin B6 and Different Heteroaromatic Nucleus." Letters in Drug Design & Discovery 16, no. 7 (2019): 792–98. http://dx.doi.org/10.2174/1570180815666180627122055.

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Background: The term vitamin B6 refers to a set of six compounds, pyridoxine,pyridoxal ,and pyridoxamine and their phosphorylated forms, among which pyridoxal 5´-phosphate (PLP) is the most important and active form acting as a critical cofactor. These compounds are very useful in medicinal chemistry because of their structure and functionalities and are also used in bioinorganic chemistry as ligands for complexation with metals. Methods: In this study, a series of hydrazones 1a-g and N-acylhydrazones 2a-f containing vitamin B6 have been synthesized from commercial pyridoxal hydrochloride and
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Chen, Xuyang, Hui Li, Hongjun Luo, Zhexuan Lin, and Wenhong Luo. "Synthesis and Evaluation of Pyridoxal Hydrazone and Acylhydrazone Compounds as Potential Angiogenesis Inhibitors." Pharmacology 104, no. 5-6 (2019): 244–57. http://dx.doi.org/10.1159/000501630.

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Background/Aims: Hydrazone and acylhydrazone derivatives, which are produced from aldehyde reacting with hydrazine or acylhydrazine, have been reported to exhibit antitumor activities. However, the angionenic effects of this kind of derivatives haven’t been elucidated. Here, we synthesized 12 pyridoxal hydrazone and acylhydrazone compounds and investigated their antiangiogenic effects and the underlying mechanisms. Method: 3-(4,5-Dimethylthiazol-2-yl)-2, 5-dipheyltetrazolium bromide assay was used to screen the inhibitory effects of the synthesized compounds on endothelial cells (ECs) prolifer
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Oikawa, Eizo, Satoko Tamura, Yohsuke Arai, and Toshiki Aoki. "Synthesis of pyridine-moieties-containing poly(acylhydrazone)s and solute separation through their membranes." Journal of Applied Polymer Science 58, no. 8 (1995): 1205–19. http://dx.doi.org/10.1002/app.1995.070580801.

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Peng, Huanan, Xiaoming Peng, Jiaqi Huang, et al. "Synthesis and crystal structure of a novel pyridine acylhydrazone derivative as a “turn on” fluorescent probe for Al3+." Journal of Molecular Structure 1212 (July 2020): 128138. http://dx.doi.org/10.1016/j.molstruc.2020.128138.

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Li, Xin-yang, Shuai Li, Guo-qing Lu, et al. "Design, synthesis and biological evaluation of novel (E)-N-phenyl-4-(pyridine-acylhydrazone) benzamide derivatives as potential antitumor agents for the treatment of multiple myeloma (MM)." Bioorganic Chemistry 103 (October 2020): 104189. http://dx.doi.org/10.1016/j.bioorg.2020.104189.

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Yao, Yao, Yuan Zhang, Xiang Li, and Yong-Qing Qiu. "The second-order NLO property of a photoswitchable heteroditpioc ion-pair receptor based on 2-pyridyl acylhydrazone linking with 2,6-pyridine bisamide: The impacts of metal cations and anions." Journal of Molecular Graphics and Modelling 100 (November 2020): 107652. http://dx.doi.org/10.1016/j.jmgm.2020.107652.

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Li, Jian-Ping, Ping Liu, and Yu-Lu Wang. "An Efficient and Convenient Method for the synthesis of Acyldiazenes from Acylhydrazines." Journal of Chemical Research 2003, no. 2 (2003): 109–10. http://dx.doi.org/10.3184/030823403103173138.

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Zhu, Gui-Ying, Zhenliang Liu, Jia Wang, et al. "Syntheses of four porous 3-D Cd(ii) metal–organic frameworks from a new multidentate ligand 5-(imidazol-1-yl)-N′-(pyridin-4-ylmethylene) nicotinohydrazide and their characterization and adsorption properties." RSC Advances 10, no. 51 (2020): 30650–55. http://dx.doi.org/10.1039/d0ra05131d.

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Herein, four stable 3D porous Cd(ii)-MOFs were constructed from the multidentate acylhydrazone ligand, and their CO<sub>2</sub> adsorption properties revealed that the anions have an obvious effect on the adsorption capacities of these MOFs.
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COCCO, M. T., C. CONGIU, V. ONNIS, and A. MACCIONI. "ChemInform Abstract: Heterocyclization of Acetamidrazones. Part 1. Synthesis of 1,2,4- Triazolo(4,3-a)pyridines via Ring Closure of 6-(2-Acylhydrazino) pyridine Intermediates." ChemInform 22, no. 39 (2010): no. http://dx.doi.org/10.1002/chin.199139166.

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Cocco, Maria Teresa, Cenzo Congiu, Valentina Onnis, and Antonio Maccioni. "Heterocyclization of Acetamidrazones.I.Synthesis of 1,2,4-triazolo[4,3-a]pyridinesviaring closure of 6-(2-acylhydrazino)pyridine intermediates." Journal of Heterocyclic Chemistry 28, no. 3 (1991): 797–800. http://dx.doi.org/10.1002/jhet.5570280343.

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Dissertations / Theses on the topic "Acylhydrazone pyridine"

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Marshall, Tracey. "Dynamic chemistry : nucleobase recognition by synthetic receptors and cis-trans acylhydrazone isomerism." Thesis, Bordeaux 1, 2012. http://www.theses.fr/2012BOR14477/document.

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Chimie dynamique: reconnaissance de nucléobases par des récepteurs synthétiques et isomérie cis-trans d'hydrazones acylées.Ce travail traite du développement des systèmes moléculaires qui peuvent s'adapter à l'addition de substances qui agissent comme un gabarit. Cette approche permet d'isoler une espèce majeure à partir d'un mélange de composés par le biais de la chimie combinatoire dynamique (CCD). La première partie de ma thèse de doctorat inclus l'utilisation d'un ADN simple brin (ADNsb) comme un gabarit pour le transfert d'information par auto-assemblage de récepteurs sans avoir besoin d'
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Book chapters on the topic "Acylhydrazone pyridine"

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Lindsley, C. W., and M. E. Layton. "Cyclization of 3-(Acylhydrazino)pyridin-2-amines." 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-017-00601.

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