Log in

Relevant bibliographies by topics / 3-hydroxypyridine / Journal articles

To see the other types of publications on this topic, follow the link: 3-hydroxypyridine.

Journal articles on the topic '3-hydroxypyridine'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic '3-hydroxypyridine.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Koch, Volker, and Stefan Schnatterer. "Chemistry of 3-Hydroxypyridine Part 1: Bromination and Iodination of 3-Hydroxypyridine." Synthesis 1990, no. 06 (1990): 497–98. http://dx.doi.org/10.1055/s-1990-26918.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Gao, Shan, Xian-Fa Zhang, Li-Hua Huo, Zhen-Zhong Lu, Hui Zhao, and Jing-Gui Zhao. "Dichlorotetrakis(3-hydroxypyridine)cobalt(II)." Acta Crystallographica Section E Structure Reports Online 60, no. 8 (2004): m1128—m1130. http://dx.doi.org/10.1107/s160053680401712x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Den Hertog, H. J., F. R. Schepman, J. de Bruyn, and G. J. E. Thysse. "Bromo-derivatives of 3-hydroxypyridine." Recueil des Travaux Chimiques des Pays-Bas 69, no. 10 (2010): 1281–88. http://dx.doi.org/10.1002/recl.19500691011.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Nifant'ev, �. E., M. A. Kharshan, A. N. Khailova, V. I. Kuz'min, and E. E. Milliaresi. "Synthesis of 3-hydroxypyridine phosphates." Chemistry of Heterocyclic Compounds 24, no. 1 (1988): 112. http://dx.doi.org/10.1007/bf00475585.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Prins, D. A. "The methylation of 3-hydroxypyridine." Recueil des Travaux Chimiques des Pays-Bas 76, no. 1 (2010): 58–64. http://dx.doi.org/10.1002/recl.19570760107.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Zhang, Xian-Fa, Shan Gao, Li-Hua Huo, Zhen-Zhong Lu та Hui Zhao. "Dichlorotetrakis(3-hydroxypyridine-κN)nickel(II)". Acta Crystallographica Section E Structure Reports Online 60, № 10 (2004): m1367—m1369. http://dx.doi.org/10.1107/s1600536804021245.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Hsieh, Yih-Huang, Noham Weinberg, and Saul Wolfe. "Co-operative hydration of the carbonyl group — "Bifunctional catalysis" by 2-hydroxypyridine is achieved via a dihydrate of 2-pyridone." Canadian Journal of Chemistry 86, no. 2 (2008): 81–90. http://dx.doi.org/10.1139/v07-074.

Full text

Abstract:

Although 2-hydroxypyridine is one thousand times less acidic than its isomer 3-hydroxypyridine and ten million times less acidic than acetic acid, in the aqueous hydration of 1 mol/L acetone at 298 K the catalytic effect of added 2-hydroxypyridine is 600 000 times greater than that of 3-hydroxypyridine and 20 times greater than that of acetic acid. This experimental result is successfully reproduced by a theoretical treatment that assumes that solvent molecules participate in a cyclic cooperative mechanism that avoids the formation of charged intermediates. However, the theoretical treatment d

APA, Harvard, Vancouver, ISO, and other styles

10

Burnett, Christina L., Wilma F. Bergfeld, Donald V. Belsito, et al. "Safety Assessment of 2-Amino-3-Hydroxypyridine as Used in Cosmetics." International Journal of Toxicology 39, no. 2_suppl (2020): 91S—97S. http://dx.doi.org/10.1177/1091581820952376.

Full text

Abstract:

The Expert Panel for Cosmetic Ingredient Safety (Panel) reviewed the safety of 2-Amino-3-Hydroxypyridine, which is reported to function as an oxidative hair dye ingredient. The Panel reviewed relevant animal and human data provided in this safety assessment, and concluded that 2-Amino-3-Hydroxypyridine is safe in the present practices of use and concentration for use in oxidative hair dye formulations.

APA, Harvard, Vancouver, ISO, and other styles

11

Sabot, Cyrille, Afef Mabrouki, Patricia Le Nahenec-Martel, Abdelkader Kriaa, Ahmed Hedhli, and Pierre-Yves Renard. "Dearomatization of a 3-Hydroxypyridine Through an Unexpected Oxidative Deformylation Process: An Entry to Azacyclohexadienones." Synlett 31, no. 15 (2020): 1497–500. http://dx.doi.org/10.1055/s-0040-1706870.

Full text

Abstract:

Phenols are well-known precursors of cyclohexadienones, which have widespread applications in organic synthesis. In contrast, their hydroxypyridine counterparts have not been explored yet. An unprecedented oxidative dearomatization of a 3-hydroxypyridine involving an unexpected deformylation step is reported. The chemical reactivity of the resulting unreported azacyclohexadiene-type compound was also explored.

APA, Harvard, Vancouver, ISO, and other styles

12

Huq, Fazlul, and Jun Qing Yu. "Molecular modeling analysis: "Why is 2-hydroxypyridine soluble in water but not 3-hydroxypyridine?"." Journal of Molecular Modeling 8, no. 3 (2002): 81–86. http://dx.doi.org/10.1007/s00894-002-0073-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Yasnetsov, V. V., Yu V. Ivanov, Vik V. Yasnetsov, S. К. Karsanova, and N. А. Chelnaya. "NEUROPROTECTIVE PROPERTIES OF NEW 3-HYDROXYPYRIDINE DERIVATIVES." Aerospace and Environmental Medicine 53, no. 1 (2019): 74–78. http://dx.doi.org/10.21687/0233-528x-2019-53-1-74-78.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Zhang, Xue-Li, Yu-Juan Lu, Ji-Zhen Li, and Seik Weng Ng. "Hexaaquazinc(II) bis(6-hydroxypyridine-3-carboxylate)." Acta Crystallographica Section E Structure Reports Online 61, no. 6 (2005): m1063—m1064. http://dx.doi.org/10.1107/s1600536805013917.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Zhang, Xue-Li, and Seik Weng Ng. "Hexaaquacobalt(II) bis(6-hydroxypyridine-3-carboxylate)." Acta Crystallographica Section E Structure Reports Online 61, no. 6 (2005): m1140—m1141. http://dx.doi.org/10.1107/s1600536805014911.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Zhang, Xue-Li, and Seik Weng Ng. "Hexaaquanickel(II) bis(6-hydroxypyridine-3-carboxylate)." Acta Crystallographica Section E Structure Reports Online 61, no. 6 (2005): m1142—m1143. http://dx.doi.org/10.1107/s1600536805014923.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Tian, Guang-Ru, Ru-Fen Zhang, Chun-Lin Ma, and Seik Weng Ng. "Bis(3-hydroxypyridine-2-carboxylato)dimethyltin(IV)." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): m2276—m2277. http://dx.doi.org/10.1107/s1600536805032277.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Shi, Jing-Min, Hai-Yan Xu, and Lian-Dong Liu. "Diaquabis(3-hydroxypyridine N-oxide)dithiocyanatocobalt(II)." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (2006): m1577—m1578. http://dx.doi.org/10.1107/s1600536806022185.

Full text

Abstract:

In the title mononuclear complex, [Co(NCS)2(C5H5NO2)2(H2O)2], the six-coordinated CoII atom lies on an inversion center. In the crystal structure, intermolecular O—H...O (H...O = 1.85–2.01 Å) and O—H...S (H...S = 2.40 Å) hydrogen bonds link molecules into a three-dimensional network.

APA, Harvard, Vancouver, ISO, and other styles

19

Li, Jun-Hua, Jing-Jing Nie та Duan-Jun Xu. "Bis(3-hydroxypyridine-κN)bis(3-nitrobenzoato-κO)zinc(II)". Acta Crystallographica Section E Structure Reports Online 65, № 8 (2009): m927. http://dx.doi.org/10.1107/s1600536809027147.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Yasuda, Mari, Takeshi Sakamoto, Reiko Sashida, Makoto Ueda, Yuuki Morimoto, and Toru Nagasawa. "Microbial Hydroxylation of 3-Cyanopyridine to 3-Cyano-6-hydroxypyridine." Bioscience, Biotechnology, and Biochemistry 59, no. 4 (1995): 572–75. http://dx.doi.org/10.1271/bbb.59.572.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Staun, Selena L., and Allen G. Oliver. "4-Pyridone–terephthalic acid–water (2/1/2) and bis(3-hydroxypyridinium) terephthalate." Acta Crystallographica Section C Crystal Structure Communications 68, no. 2 (2012): o84—o87. http://dx.doi.org/10.1107/s0108270111055260.

Full text

Abstract:

4-Hydroxypyridine and terephthalic acid cocrystallize as a hydrate, 4-pyridone–terephthalic acid–water (2/1/2), 2C5H5NO·C8H6O4·2H2O, from a methanol–water solution. The molecules form a two-dimensional hydrogen-bonded network resulting in sheets of hydrogen-bonded molecules that lie parallel to the (10\overline 2) plane. In contrast, 3-hydroxypyridine and terephthalic acid form the salt bis(3-hydroxypyridinium) terephthalate, 2C5H6NO+·C8H4O42−, giving rise to two-dimensional hydrogen-bonded sheets extending through the lattice parallel to the (10\overline 2) plane.

APA, Harvard, Vancouver, ISO, and other styles

22

Farhadikoutenaei, Abbas, Kaliyaperumal Thanigaimani, Suhana Arshad, and Ibrahim Abdul Razak. "2-Amino-5-methylpyridinium 3-hydroxypyridine-2-carboxylate." Acta Crystallographica Section E Structure Reports Online 69, no. 7 (2013): o1118—o1119. http://dx.doi.org/10.1107/s1600536813016322.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Voronina, T. A., and O. A. Kutepova. "Experimentally established geropsychotropic properties of 3-hydroxypyridine antioxidant." Drug Development Research 14, no. 3-4 (1988): 353–58. http://dx.doi.org/10.1002/ddr.430140329.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Huq, Fazlul, Hasan Tayyem, Philip Beale, and Jun Qing Yu. "Studies on the activity of three palladium(II) compounds of the form: Trans-PdL2Cl2 where L=2-hydroxypyridine, 3-hydroxypyridine, and 4-hydroxypyridine." Journal of Inorganic Biochemistry 101, no. 1 (2007): 30–35. http://dx.doi.org/10.1016/j.jinorgbio.2006.08.001.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Vaitekūnas, Justas, Renata Gasparavičiūtė, Jonita Stankevičiūtė, Gintaras Urbelis, and Rolandas Meškys. "Biochemical and Genetic Analysis of 4-Hydroxypyridine Catabolism in Arthrobacter sp. Strain IN13." Microorganisms 8, no. 6 (2020): 888. http://dx.doi.org/10.3390/microorganisms8060888.

Full text

Abstract:

N-Heterocyclic compounds are widely spread in the biosphere, being constituents of alkaloids, cofactors, allelochemicals, and artificial substances. However, the fate of such compounds including a catabolism of hydroxylated pyridines is not yet fully understood. Arthrobacter sp. IN13 is capable of using 4-hydroxypyridine as a sole source of carbon and energy. Three substrate-inducible proteins were detected by comparing protein expression profiles, and peptide mass fingerprinting was performed using MS/MS. After partial sequencing of the genome, we were able to locate genes encoding 4-hydroxyp

APA, Harvard, Vancouver, ISO, and other styles

26

Bu, Junru, Huan Liu, and Chunmian Lin. "Fenton's reagent-enhanced supercritical water oxidation of wastewater released from 3-hydroxypyridine production." RSC Advances 9, no. 50 (2019): 29317–26. http://dx.doi.org/10.1039/c9ra05510j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Chen, Chang-nan, Ming-chu Wu, Andrew Yeh, and Thomas Y. R. Tsai. "4- and 3-Hydroxypyridine complexes of pentacyanoferrate(II, III)." Inorganica Chimica Acta 267, no. 1 (1998): 81–86. http://dx.doi.org/10.1016/s0020-1693(97)05557-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Lu, Zhen-Zhong, Li-Hua Huo, Shan Gao, Hui Zhao та Jing-Gui Zhao. "Bis(3-hydroxypyridine-κN)(nitrato-κ2O,O′)silver(I)". Acta Crystallographica Section E Structure Reports Online 61, № 7 (2005): m1386—m1388. http://dx.doi.org/10.1107/s1600536805019240.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Zolotov, N. N., L. D. Smirnov, V. I. Kuz'min, et al. "Derivatives of 3-hydroxypyridine as inhibitors of proteolytic enzymes." Pharmaceutical Chemistry Journal 23, no. 2 (1989): 89–91. http://dx.doi.org/10.1007/bf00764451.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Lukyanova, L. D., E. L. Germanova, T. A. Tsybina, and G. N. Chernobaeva. "Energotropic Effect of Succinate-Containing Derivatives of 3-Hydroxypyridine." Bulletin of Experimental Biology and Medicine 148, no. 4 (2009): 587–91. http://dx.doi.org/10.1007/s10517-010-0771-0.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Ji, Hong-Fang, and Liang Shen. "Mechanisms of singlet and triplet state riboflavin quenching by 3-hydroxypyridine and 4-hydroxypyridine. A quantum chemical study." Journal of Molecular Structure: THEOCHEM 865, no. 1-3 (2008): 25–27. http://dx.doi.org/10.1016/j.theochem.2008.06.012.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Wang, Ye, Hang Yin, Ying Shi, Mingxing Jin, and Dajun Ding. "Ground-state and excited-state multiple proton transfer via a hydrogen-bonded water wire for 3-hydroxypyridine." New J. Chem. 38, no. 9 (2014): 4458–64. http://dx.doi.org/10.1039/c4nj00458b.

Full text

Abstract:

The multiple proton transfer reactions of 3-hydroxypyridine-(H<sub>2</sub>O)<sub>3</sub> have been demonstrated, and a perfect proton transfer cycle has been revealed in the ground and excited states.

APA, Harvard, Vancouver, ISO, and other styles

33

Zamotaeva, M. N., V. I. Inchina, V. V. Konorev, Yu V. Kuznetsov, and N. D. Kuz’michev. "Evaluation of the Possibility of Correction of Doxorubicin-Induced Chronic Heart Failure in the Experiment with 3-Hydroxypyridine Acetylcysteinate and 3-Hydroxypyridine Succinate." Bulletin of Experimental Biology and Medicine 165, no. 3 (2018): 344–46. http://dx.doi.org/10.1007/s10517-018-4166-y.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Perdih, Franc. "Copper(II) bis(4,4,4-trifluoro-1-phenylbutane-1,3-dionate) complexes with pyridin-2-one, 3-hydroxypyridine and 3-hydroxypyridin-2-one ligands: molecular structures and hydrogen-bonded networks." Acta Crystallographica Section C Structural Chemistry 73, no. 11 (2017): 960–67. http://dx.doi.org/10.1107/s2053229617014875.

Full text

Abstract:

Copper(II) bis(4,4,4-trifluoro-1-phenylbutane-1,3-dionate) complexes with pyridin-2-one (pyon), 3-hydroxypyridine (hpy) and 3-hydroxypyridin-2-one (hpyon) were prepared and the solid-state structures of (pyridin-2-one-κO)bis(4,4,4-trifluoro-3-oxo-1-phenylbutan-1-olato-κ2 O,O′)copper(II), [Cu(C10H6F3O2)2(C5H5NO)] or [Cu(tfpb-κ2 O,O′)2(pyon-κO)], (I), bis(pyridin-3-ol-κO)bis(4,4,4-trifluoro-3-oxo-1-phenylbutan-1-olato-κ2 O,O′)copper(II), [Cu(C10H6F3O2)2(C5H5NO)2] or [Cu(tfpb-κ2 O,O′)2(hpy-κO)2], (II), and bis(3-hydroxypyridin-2-one-κO)bis(4,4,4-trifluoro-3-oxo-1-phenylbutan-1-olato-κ2 O,O′)coppe

APA, Harvard, Vancouver, ISO, and other styles

35

Wang, Pin-Liang, Hai-Su Zeng, Si-Shun Kang, and Hai-Bo Wang. "2-Chloro-3-(2,2,2-trifluoroethoxy)pyridine." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4355. http://dx.doi.org/10.1107/s1600536807050337.

Full text

Abstract:

The title compound, C7H5ClF3NO, was synthesized by the reaction of 2-chloro-3-hydroxypyridine with 2-chloro-1,1,1-trifluoroethane. The pyridine ring and the O and Cl atoms are nearly coplanar, the largest deviation from the mean plane being 0.078 (6) Å. Bioassay indicates that the title compound has a good fungicidal activity.

APA, Harvard, Vancouver, ISO, and other styles

36

Zevin, S., G. Link, RW Grady, RC Hider, HH Peter, and C. Hershko. "Origin and fate of iron mobilized by the 3-hydroxypyridin-4-one oral chelators: studies in hypertransfused rats by selective radioiron probes of reticuloendothelial and hepatocellular iron stores." Blood 79, no. 1 (1992): 248–53. http://dx.doi.org/10.1182/blood.v79.1.248.248.

Full text

Abstract:

Abstract The mechanism of in vivo iron chelation by 3-hydroxypyridin-4-ones (CP compounds) was studied in hypertransfused rats in which the major storage iron pools in hepatocytes and in the reticuloendothelial (RE) system have been labeled by selective radioiron probes. Both dimethyl-3- hydroxypyridin-4-one (CP 20 or L1) and diethyl-3-hydroxypyridine-4-one (CP 94) have an identical and very high (log beta 3 36) binding constant and selective affinity to iron(III), but the lipid solubility of CP 94 is considerably higher than that of CP 20. Both chelators induced an increase in the fecal excre

APA, Harvard, Vancouver, ISO, and other styles

37

Zevin, S., G. Link, RW Grady, RC Hider, HH Peter, and C. Hershko. "Origin and fate of iron mobilized by the 3-hydroxypyridin-4-one oral chelators: studies in hypertransfused rats by selective radioiron probes of reticuloendothelial and hepatocellular iron stores." Blood 79, no. 1 (1992): 248–53. http://dx.doi.org/10.1182/blood.v79.1.248.bloodjournal791248.

Full text

Abstract:

The mechanism of in vivo iron chelation by 3-hydroxypyridin-4-ones (CP compounds) was studied in hypertransfused rats in which the major storage iron pools in hepatocytes and in the reticuloendothelial (RE) system have been labeled by selective radioiron probes. Both dimethyl-3- hydroxypyridin-4-one (CP 20 or L1) and diethyl-3-hydroxypyridine-4-one (CP 94) have an identical and very high (log beta 3 36) binding constant and selective affinity to iron(III), but the lipid solubility of CP 94 is considerably higher than that of CP 20. Both chelators induced an increase in the fecal excretion of h

APA, Harvard, Vancouver, ISO, and other styles

38

Musser, Steven M., Martha L. Gay, Eugene P. Mazzola, and Ronald D. Plattner. "Identification of a New Series of Fumonisins Containing 3-Hydroxypyridine." Journal of Natural Products 59, no. 10 (1996): 970–72. http://dx.doi.org/10.1021/np960349t.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Huq, Fazlul, Muhammed Danish, Wojciech Starosta та Janusz Leciejewicz. "trans-Bis(3-hydroxypyridine-κN)diiodidoplatinum(II) dimethyl sulfoxide disolvate". Acta Crystallographica Section E Structure Reports Online 67, № 6 (2011): m721. http://dx.doi.org/10.1107/s1600536811015893.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Gao, Shan, Xian-Fa Zhang, Li-Hua Huo та Hui Zhao. "Tetr-μ-acetato-κ8O:O′-bis[(3-hydroxypyridine-κN)copper(II)]". Acta Crystallographica Section E Structure Reports Online 60, № 10 (2004): m1405—m1407. http://dx.doi.org/10.1107/s1600536804021993.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Albada, Gerard A. van, Ilpo Mutikainen, Urho Turpeinen та Jan Reedijk. "catena-Poly[[dicyanamidobis(3-hydroxypyridine-N)copper(II)]-μ-dicyanamido]". Acta Crystallographica Section E Structure Reports Online 57, № 10 (2001): m421—m423. http://dx.doi.org/10.1107/s160053680101460x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Blinov, D. S., L. N. Sernov, V. P. Balashov, et al. "Antiischemic Activity of New Domestic Antioxidant 3-Hydroxypyridine Etoxidol Derivative." Bulletin of Experimental Biology and Medicine 152, no. 5 (2012): 583–86. http://dx.doi.org/10.1007/s10517-012-1581-3.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Yasnetsov, Vic V., S. Ya Skachilova, L. N. Sernov, T. A. Voronina, and V. V. Yasnetsov. "Synthesis and pharmacological properties of a new 3-hydroxypyridine derivative." Pharmaceutical Chemistry Journal 46, no. 4 (2012): 199–202. http://dx.doi.org/10.1007/s11094-012-0760-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Zherdev, V. P., A. K. Sariev, A. A. Dvoryaninov, T. A. Voronina, and L. D. Smirnov. "Pharmacokinetics of a water-soluble antioxidant of 3-hydroxypyridine type." Bulletin of Experimental Biology and Medicine 101, no. 3 (1986): 333–35. http://dx.doi.org/10.1007/bf00835938.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Val'dman, A. V., T. A. Voronina, L. D. Smirnov, U. M. Tilekeeva, and K. M. Kyumaev. "Effect of 3-hydroxypyridine derivatives on the central nervous system." Bulletin of Experimental Biology and Medicine 99, no. 1 (1985): 73–75. http://dx.doi.org/10.1007/bf00806617.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Kremer, Marius, and Ulli Englert. "Zn and Ni complexes of pyridine-2,6-dicarboxylates: crystal field stabilization matters!" Acta Crystallographica Section E Crystallographic Communications 75, no. 6 (2019): 903–11. http://dx.doi.org/10.1107/s2056989019007461.

Full text

Abstract:

Six reaction products of ZnII and NiII with pyridine-2,6-dicarboxylic acid (H2Lig1), 4-chloropyridine-2,6-dicarboxylic acid (H2Lig2) and 4-hydroxypyridine-2,6-dicarboxylic acid (H2Lig3) are used to pinpoint the structural consequences of crystal field stabilization by an incomplete d shell. The pseudo-octahedral ZnII coordination sphere in bis(6-carboxypicolinato)zinc(II) trihydrate, [Zn(C7H4NO4)2]·3H2O or [Zn(HLig1)2]·3H2O, (1), is significantly less regular than that about NiII in the isostructural compound bis(6-carboxypicolinato)nickel(II) trihydrate, [Ni(C7H4NO4)2]·3H2O or [Ni(HLig1)2]·3H

APA, Harvard, Vancouver, ISO, and other styles

47

Patiño, J., M. C. Gutiérrez, D. Carriazo, et al. "DES assisted synthesis of hierarchical nitrogen-doped carbon molecular sieves for selective CO2versus N2 adsorption." J. Mater. Chem. A 2, no. 23 (2014): 8719–29. http://dx.doi.org/10.1039/c4ta00562g.

Full text

Abstract:

Deep eutectic solvents composed of resorcinol, 3-hydroxypyridine and tetraethylammonium bromide have been used for the synthesis of hierarchical nitrogen-doped carbon molecular sieves highly suitable for CO<sub>2</sub> adsorption.

APA, Harvard, Vancouver, ISO, and other styles

48

Fekete, M., C. Gibard, G. J. Dear, et al. "Utilisation of water soluble iridium catalysts for signal amplification by reversible exchange." Dalton Transactions 44, no. 17 (2015): 7870–80. http://dx.doi.org/10.1039/c5dt00311c.

Full text

Abstract:

The catalytic hyperpolarisation of pyridine, 3-hydroxypyridine and oxazol by the Signal Amplification By Reversible Exchange (SABRE) process is achieved by a series of water soluble iridium phosphine and N-heterocyclic carbene dihydride complexes.

APA, Harvard, Vancouver, ISO, and other styles

49

Melandri, Sonia, Luca Evangelisti, Sofia Canola, et al. "Chlorination and tautomerism: a computational and UPS/XPS study of 2-hydroxypyridine ⇌ 2-pyridone equilibrium." Physical Chemistry Chemical Physics 22, no. 24 (2020): 13440–55. http://dx.doi.org/10.1039/d0cp02304c.

Full text

Abstract:

Disentangling complex photoelectronic spectral features through computational studies allows to achieve a precise description of the tautomeric equilibrium in the neutral and cationic states of parent, 3-Cl, 4-Cl, 5-Cl and 6-Cl 2-hydroxypyridine.

APA, Harvard, Vancouver, ISO, and other styles

50

Sakagami, Hideki, Takashi Kamikubo, and Kunio Ogasawara. "A Facile Synthesis of (R)-4-Amino-3-hydroxybutanoic Acid (GABOB) from 3-Hydroxypyridine." Synlett 1997, no. 2 (1997): 221–22. http://dx.doi.org/10.1055/s-1997-744.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!