Relevant bibliographies by topics / 3-hydroxypyridines

Contents

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

Academic literature on the topic '3-hydroxypyridines'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "3-hydroxypyridines"

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Koch, Volker, and Stefan Schnatterer. "Chemistry of 3-Hydroxypyridine Part 2: Synthesis of 5,6-Dihalo-3-hydroxypyridines." Synthesis 1990, no. 06 (1990): 499–501. http://dx.doi.org/10.1055/s-1990-26919.

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Fürst, Michael C. D., Leonard R. Bock, and Markus R. Heinrich. "Regioselective Radical Arylation of 3-Hydroxypyridines." Journal of Organic Chemistry 81, no. 13 (2016): 5752–58. http://dx.doi.org/10.1021/acs.joc.6b00894.

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Ito, Kazuya, Takayuki Doi, and Hirokazu Tsukamoto. "De Novo Synthesis of Polysubstituted 3-Hydroxypyridines Via “Anti-Wacker”-Type Cyclization." Catalysts 13, no. 2 (2023): 319. http://dx.doi.org/10.3390/catal13020319.

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We report an efficient method to prepare polysubstituted 3-hydroxypyridines from amino acids, propargyl alcohols, and arylboronic acids. The process involves Pd(0)-catalyzed anti-selective arylative cyclizations of N-propargyl-N-tosyl-aminoaldehydes with arylboronic acids (“anti-Wacker”-type cyclization), oxidation of the resulting 5-substituted-3-hydroxy-1,2,3,6-tetrahydropyridines to 3-oxo derivatives, and elimination of p-toluenesulfinic acid. This method provides diverse polysubstituted 3-hydroxypyridines, whose hydroxy group can be further substituted by a cross-coupling reaction via a tr
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Fuss, Andreas, and Volker Koch. "Chemistry of 3-Hydroxypyridine Part 3: Synthesis of Substituted 3-[Fluoro(chloro)alkoxy]pyridines from Halo- or Amino-3-hydroxypyridines." Synthesis 1990, no. 07 (1990): 604–8. http://dx.doi.org/10.1055/s-1990-26956.

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Asami, Tadao, Masatoshi Baba, Hiroyuki Koike, Yorinao Inoue, and Shigeo Yoshida. "Halogenation Enhances the Photosystem II Inhibitory Activity of 4-Hydroxypyridines: Structure-Activity Relationships and Their Mode of Action." Zeitschrift für Naturforschung C 48, no. 3-4 (1993): 152–58. http://dx.doi.org/10.1515/znc-1993-3-407.

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Abstract A range of 4-hydroxypyridines were synthesized and their activity as PET inhibitors were investigated with regard to their structural resemblance to plastoquinone in photosynthetic electron transport (PET). The activity of these compounds was markedly enhanced upon modifying their structures: introduction of halogens into both the 3-and 5-positions of the pyridine ring and additional substitution at the α-position of the side chain at 6-position were effective among others in enhancing the activity. Insertion of a phenyl ring into the side chain at 6-position of the pyridine ring also
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Kuz'min, V. I., A. S. Losev, I. S. Morozov, et al. "Synthesis and biological activity of 2-phenylethyl-3-hydroxypyridines." Pharmaceutical Chemistry Journal 27, no. 8 (1993): 555–61. http://dx.doi.org/10.1007/bf00779915.

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Erhardt, Hellmuth, Kevin A. Kunz, and Stefan F. Kirsch. "Thermolysis of Geminal Diazides: Reagent-Free Synthesis of 3-Hydroxypyridines." Organic Letters 19, no. 1 (2016): 178–81. http://dx.doi.org/10.1021/acs.orglett.6b03475.

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Amat-Guerri, F., A. Pajares, J. Gianotti, et al. "Singlet molecular oxygen-mediated photooxidation of 2-substituted 3-hydroxypyridines." Journal of Photochemistry and Photobiology A: Chemistry 126, no. 1-3 (1999): 59–64. http://dx.doi.org/10.1016/s1010-6030(99)00115-x.

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Lin, Shaw-Tao, Ling-Ling Tien, Yueh-Hsiung Kuo, and Kae-Shyang Shih. "Mass spectra of 2- and/or 6-alkyl-3-hydroxypyridines." Organic Mass Spectrometry 26, no. 6 (1991): 583–86. http://dx.doi.org/10.1002/oms.1210260609.

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Nesterova, Natalia I., Olesya V. Shcheblykina, Pavel D. Kolesnichenko, Arkady V. Nesterov, Dmitry V. Shcheblykin, and Dmitry Yakovlev. "Neuroprotective effects of taurine and 3-hydroxypyridine derivatives in the intracerebral hemorrhage model in rats." Research Results in Pharmacology 5, no. (3) (2019): 87–94. https://doi.org/10.3897/rrpharmacology.5.36988.

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Introduction: At present, the problem of pharmacological correction of free radical processess emerges full-blown. The aim of the study is an experimental study of the neuroprotective effect of taurine and 3-hydroxypyridine derivatives. Materials and methods: The study was performed in Wistar rats. The neuroprotective effect of the substances was studied in the intracerebral hemorrhage model. Results and discussion: The administration of the studied substances had a positive effect on the survival of the animals within the first day (50% of rats died in the control group, 30% – in the Mexidol-
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Dissertations / Theses on the topic "3-hydroxypyridines"

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Chubb, Richard William John. "New functionalised 3-hydroxypyridines." Thesis, Durham University, 2001. http://etheses.dur.ac.uk/4214/.

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This thesis is concerned with the synthesis and reactions of functionalised 3- liydroxypyridines, in particular 2-aryl- and 2-heteroary 1-3-liydroxypyridines by non- coupling methodology, from furan precursors. Chapter 1 reviews the synthesis and reactions of 3-hydroxypyridines. Chapter 2 describes the synthesis of 2-acylfurans via differing methods, which include acylation of the furan nucleus, Grignard reactions of furaldehydes and, most notably, reaction of lithiofurans with reagents containing a nitrile component. Chapter 3 concerns reaction of acylfurans with ammonia at high pressure and
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Wolken, Jill K. "A neutralization-reionization mass spectrometry and computational analysis of 3-hydroxypyridine, 2-hydroxypyridine/2-(1H)pyridone, and uracil /." Thesis, Connect to this title online; UW restricted, 2000. http://hdl.handle.net/1773/8659.

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Karvelis, Laimonas. "Investigation of the Degradation of Carboxypyridines in Bacteria." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2012. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2012~D_20121001_092919-52075.

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The main aim of this work was the study of bacteria capable to degrade the pyridine monocarboxylic acids. Achromobacter sp. strain JS18 capable to utilize 3-hydroxypyridine- 2-carboxylic acid was selected by screening of microorganisms hydroxylating the pyridine ring at unusual positions or transforming pyridine derivatives . The strain 5HP consuming 5- hydroxypyridine-2-carboxylic acid as a sole carbon and energy source was isolated from soil. The 16S rRNA-based phylogenetic analysis showed that the isolate belongs to Pusillimonas genus. It was found that picolinic, nicotinic and dipicolinic
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Karvelis, Laimonas. "Karboksipiridinų degradacijos bakterijose tyrimas." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2012. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2012~D_20121001_092930-97592.

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Šio darbo metu buvo tiriamos bakterijos, galinčios skaidyti piridino monokarboksirūgštis. Netradicinėse vietose hidroksilinančių ir/ar hidroksilintų pikolino ir nikotino rūgščių skaidyme dalyvaujančių mikroorganizmų atranka leido identifikuoti Achromobacter sp. JS18 bakteriją, skaidančią 3-hidroksipiridino-2-karboksirūgštį, ir iš dirvožemio išskirti 5HP kamieną, galintį panaudoti 5-hidroksipiridino-2-karboksirūgštį vieninteliu anglies ir energijos šaltiniu. 16S rRNR geno analizės duomenimis 5HP kamienas priklauso Pusillimonas genčiai. Tai pirmoji žinoma bakterija, galinti skaidyti 5- hidroksip
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Ako, Ayuk M. "Kinetics and mechanisms of the aqueous bromination of 3-hydroxypyridines." Thesis, 1991. http://spectrum.library.concordia.ca/3562/1/MM73707.pdf.

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Lu, Jin-Yong [Verfasser]. "Development of a Hetero-Diels-Alder reaction to synthesize 3-hydroxypyridines and its application toward the total synthesis of nosiheptide / von Jin-Yong Lu." 2009. http://d-nb.info/996069402/34.

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Book chapters on the topic "3-hydroxypyridines"

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Bährle-Rapp, Marina. "2-Amino-3-Hydroxypyridine." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_490.

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Bährle-Rapp, Marina. "5-Amino-2,6-Dimethoxy-3-Hydroxypyridine." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_482.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) chloride complex of 3-hydroxypyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_540.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) chloride complex of 3-hydroxypyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_713.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) chloride complex of 4-chloro-3-hydroxypyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_545.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) chloride complex of 4-chloro-3-hydroxypyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_541.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper chloro complex with 2-(dimethylamino-methyl)-3-hydroxypyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_226.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper bromo complex with 2-(dimethylamino-methyl)-3-hydroxypyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_227.

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Brissette, Pierre, David P. Ballou, and Vincent Massey. "The oxidative half-reaction of 2-methyl-3-hydroxypyridine-5 - carboxylic acid oxygenase from Pseudomonas sp. MA-1." In Flavins and Flavoproteins 1987, edited by D. E. Edmondson and D. B. McCormick. De Gruyter, 1987. http://dx.doi.org/10.1515/9783110884715-098.

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Ueda, M., M. Yasuda, T. Sakamoto, and Y. Morimoto. "High level production of 3-cyano-6-hydroxypyridine from 3-cyanopyridine by Comamonas testosteroni MCI2848." In Studies in Organic Chemistry. Elsevier, 1998. http://dx.doi.org/10.1016/s0165-3253(98)80017-5.

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Conference papers on the topic "3-hydroxypyridines"

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Simakina, Ekaterina, Sofya Skachilova, Victor Yasnetsov, Alexandra Yurochkina, Tatiana Voronina, and Andrey Denisenko. "3-HYDROXYPYRIDINE DERIVATIVES, POSSESSING NEUROPROTECTIVE ACTIVITY." In XVI International interdisciplinary congress "Neuroscience for Medicine and Psychology". LLC MAKS Press, 2020. http://dx.doi.org/10.29003/m1253.sudak.ns2020-16/421-422.

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Saxena, Swasti, and Ankit K. Srivastava. "Study of vibrational modes in 3-methyl-2-hydroxypyridine: Spectroscopic analysis." In NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS: NCPCM2020. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0061174.

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Srivastava, Ankit K., and Swasti Saxena. "Ab initio study of three-fold methyl torsion in 2-methyl-3-hydroxypyridine in ground electronic state (S0)." In NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS: NCPCM2020. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0061173.

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G, Vidya V., V. Sadasivan, S. S. Meena, and Pramod Bhatt. "Synthesis and spectral study of new azo dye and its iron complexes derived from 2-naphthol and 2-amino-3-hydroxypyridine." In LIGHT AND ITS INTERACTIONS WITH MATTER. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4898308.

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You might also be interested in the extended bibliographies on the topic '3-hydroxypyridines' for particular source types:
Journal articles
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