Relevant bibliographies by topics / 2-hydroxy benzaldehyde

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

Academic literature on the topic '2-hydroxy benzaldehyde'

Author: Grafiati
Published: 7 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "2-hydroxy benzaldehyde"

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Selvarani, V., M. A. Neelakantan, V. Silambarasan, and D. Velmurugan. "2-Hydroxy-4-(prop-2-ynyloxy)benzaldehyde." Acta Crystallographica Section E Structure Reports Online 69, no. 1 (2012): o64. http://dx.doi.org/10.1107/s1600536812049598.

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Öğütçü, Hatice, Nurdan K. Yetim, Elvan H. Özkan, et al. "Nanospheres caped Pt(II) and Pt (IV): synthesis and evaluation as antimicrobial and Antifungal Agent." Polish Journal of Chemical Technology 19, no. 1 (2017): 74–80. http://dx.doi.org/10.1515/pjct-2017-0011.

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Abstract Antimicrobial and antifungal polymers are gaining the attention of pharmaceutical makers and industrial design. Nanospheres-Polymers attached Platinum(II) / (IV) complexes have been synthesized to investigate antimicrobial activities. Firstly, nanospheres involving Schiff bases were synthesized from (aminomethyl) polystyrene and four substitute salicylaldehyde (2-hydroxy benzaldehyde, 5-fluoro-2-hydroxy benzaldehyde, 5-kloro-2-hydroxy benzaldehyde, 5-bromo-2-hydroxy benzaldehyde). Secondly, polymers attached Platinum(II) / (IV) complexes have been prepared by means of template method.
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Amal S. Sadiq. "Synthesis of N-Substituted 3-Chloro- 2-azetidinones for 2, 4-diamino-6- hydroxy pyrimidin." Journal of the College of Basic Education 21, no. 88 (2023): 13–24. http://dx.doi.org/10.35950/cbej.v21i88.9949.

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This search involved synthesis of several new N-Substituted -3-chloro-
 2-azetidinones which were known as a high medicinal effectiveness for 2,
 4-Diamino-6-hydroxy pyrimidin in two steps. The first step included
 preparation Shiff bases (1-6) by condensation of 2, 4-Diamino-6-hydroxy
 pyrimidin with many substituted aldehydes(4-hydroxy benzaldehyde, 2-
 bromobenzaldehyde, 4-dimethyl amino benzaldehyde, = 4-nitro
 benzaldehyde, salicylaldehyde, 4-chlorobenzaldehyde), then the second
 step included, preparation new six azetidinones compounds (7-12) by
 r
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Peng, Wan Xi, Qiu Xue, Feng Juan Wu, Xu Zhang, and Zhong Feng Zhang. "Assessment on Environmental Friendly Characteristics of Smoked Bamboo Biomass for Building Materials." Advanced Materials Research 183-185 (January 2011): 1832–36. http://dx.doi.org/10.4028/www.scientific.net/amr.183-185.1832.

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The main constituents at 230°С were propanoic acid, 2-(aminooxy)-(16.99%) , propanamide, 2-hydroxy-n-methyl-(14.20%) , benzaldehyde, 2-methyl-(13.22%) , furfural(9.44%) , butanal, 2-methyl-(8.09%) , acetic acid(7.09%) , hydrazine, methyl-(4.14%) , etc. And the main constituents at 280°С were hydrazine, ethyl-(24.87%) , 2(3h)-furanone, dihydro-4-hydroxy-(15.24%) , phenol, 2,6-dimethoxy-(11.82%) , benzaldehyde, 2-methyl-(11.49%) , furfural(4.90%) , etc. The heat release volatiles of smoked bamboo biomass might be used as raw materials of rare biomedicines. So the smoked bamboo biomass for buildi
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Wang, Yanwei, Zhenzhen Qiu, and Hongze Liang. "5-tert-Butyl-2-hydroxy-3-(2-thienyl)benzaldehyde." Acta Crystallographica Section E Structure Reports Online 66, no. 9 (2010): o2218. http://dx.doi.org/10.1107/s1600536810030382.

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Bats, Jan W., Matthias Gerlach, Michael Reggelin, and Matthias Köck. "2-Hydroxy-4,6-dimethoxy-3-(3-methylbutanoyl)benzaldehyde." Acta Crystallographica Section C Crystal Structure Communications 63, no. 11 (2007): o664—o666. http://dx.doi.org/10.1107/s0108270107048044.

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Thejeel, Entedhar, and Athraa Hameed Mekky. "Synthesis, Absorption, Distribution, Metabolism, Excretion, Toxicology (ADMET) and molecular docking studies of some pyridin-2(1H)-one derived from a Apocynin in Thi-Qar Governorate." University of Thi-Qar Journal of Science 10, no. 2 (2023): 73–80. http://dx.doi.org/10.32792/utq/utjsci/v10i2.1089.

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The present study includes synthesized of some pyridin-2(1H)- one of 1-(4-hydroxy-3-methoxyphenyl) ethan-1-one. The [ 6-(4-hydroxy-3-methoxyphenyl) - 4 - (4-methoxyphenyl) - 2 - oxo-1,2-dihydropyridine - 3- carbonitrile, 4 - (4-bromophenyl) - 6 -(4-hydroxy-3-methoxyphenyl)-2-oxo-1,2- dihydropyridine - 3- carbonitrile, 4 - (4-bromophenyl) – 6 - (4-hydroxy-3-methoxyphenyl)-2-oxo-1, 2 - dihydropyridine - 3-carbonitrile] derivatives have been synthesized by cyclization reaction of the 1-(4-hydroxy-3-methoxyphenyl)ethan-1-one with various aldehydes (4-methoxy benzaldehyde, 4-bromo benzaldehyde ,4-d
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Odabaşoğlu, Mustafa, Orhan Büyükgüngör, B. Narayana, A. M. Vijesh, and H. S. Yathirajan. "(E)-2-Hydroxy-5-methyl-3-[(2-pyridylimino)methyl]benzaldehyde." Acta Crystallographica Section E Structure Reports Online 63, no. 4 (2007): o1916—o1918. http://dx.doi.org/10.1107/s1600536807012913.

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9

Doukeh, Rami, Maria Râpă, Ecaterina Matei, et al. "An Evaluation of Glycerol Acetalization with Benzaldehyde over a Ferromagnetic Heteropolyacid Catalyst." Catalysts 13, no. 4 (2023): 782. http://dx.doi.org/10.3390/catal13040782.

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Tungstophosphoric acid (H3PW12O40) supported on silica-coated magnetite nanoparticles has been prepared and used as a heterogeneous acid catalyst (Fe3O4@SiO2@HPW) in the condensation of benzaldehyde (B) with glycerol (Gly) for the production of cyclic acetals. Physicochemical techniques, including scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier-transform infrared spectrometry (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and N2 physisorption were used to characterize the prepared catalyst. The effect of glycerol/benzaldehyde molar ratio
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Mahdi, Huda, Azhar Hameed, Alaa Mohammed, and Issraa A. Jassem. "New Benzohydrazide Schiff Base: Synthesis, Characterization and Biological Studies." INTERNATIONAL JOURNAL OF DRUG DELIVERY TECHNOLOGY 12, no. 02 (2022): 658–61. http://dx.doi.org/10.25258/ijddt.12.2.33.

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In this study, two new Schiff bases are produced via condensation reaction of 2-hydroxy-3-methoxy benzaldehyde and 2-hydroxy benzaldehyde compounds with benzohydrazide compound. The products are investigated by fourier-transform infrared spectroscopy (FTIR), proton nuclear magnetic resonance (H-NMR), carbon-13 nuclear magnetic resonance (13C-NMR), and mass spectroscopy. Antibacterial activities of synthesized compounds are scanned versus Staphylococcus aureus (gram-positive) and Escherichia coli (gram negative) strains. The results showed that the Schiff bases compounds illustrated weak effect
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Dissertations / Theses on the topic "2-hydroxy benzaldehyde"

1

Patel, Ranjita, and Soubhagyabati Sahoo. "Effect of Solvent on Azo-Hydrazonetautomerism of 2-Hydroxy-5-(4-Nitrophenylazo) Benzaldehyde." Thesis, 2015. http://ethesis.nitrkl.ac.in/7262/1/2015_Effect_Patel_and_Sahoo.pdf.

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Azo dye has been synthesized having Donor-p-Acceptor (D-p-A) system to study the effect of solvent on the azo-hydrazone tautomerism. The relative stabilities of azo and hydrazone tautomer are examined by means of UV-Vis spectroscopic technique and are correlated with the solvent properties in neat organic solvents and in different binary solvent mixture. Due to the presence of intramolecular H-bonding, azo form predominates in most of the nonpolar and polar protic solvents. Presence of low energy CT band in basic solvents like DMF is due to the predominance of anionic hydrazone form stabilized
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Book chapters on the topic "2-hydroxy benzaldehyde"

1

Taber, Douglass. "The Betzer and Ardisson Synthesis of (+)-Discodermolide." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0085.

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( + )-Discodermolide 3, a potent anticancer agent that works synergistically with taxol, may yet prove to be clinically effective. For the synthetic material to be affordable, a highly convergent synthesis is required. Jean-François Betzer and Janick Ardisson of the Université de Cergy- Pontoise have described (Angew. Chem. Int. Ed. 2007, 46, 1917) such a synthesis, coupling 1 and 2. A central feature of their approach was the repeated application of the inherently chiral secondary organometallic reagent 5. The first use of 5 was the addition to the aldehyde 4. The product 6 was ozonized, and
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Ghosh, Joydip. "Therapeutic Efficacy of Natural Products Towards Protozoan Diseases." In Recent Trends and The Future of Antimicrobial Agents - Part I. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815079609123010009.

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The different infections caused by protozoan parasites, such as malaria, leishmaniasis, toxoplasmosis, balantidiasis, trichomoniasis, giardiasis, Chagas disease, amoebic dysentery, are responsible for considerable morbidity and mortality worldwide with desolating social and economic consequences. These protozoan diseases occur all over the world. For the treatment of these diseases, there is a lack of effective, safe, and affordable therapies. Due to the lack of vaccines in most instances and the development of resistant strains to the available synthetic therapeutics, it is important to searc
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Taber, Douglass F. "Organic Functional Group Transformation." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0007.

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Susumu Saito of Nagoya University developed (Angew. Chem. Int. Ed. 2011, 50, 3006) Fe-catalyzed conditions, compatible with alkenes, for converting an alcohol 1 to the amine 2. Corey R. J. Stephenson of Boston University took advantage (Nature Chem. 2011, 3, 140) of photoredox catalysis to convert an alcohol 3 to the iodide 4. Jing-Mei Huang of the South China University of Technology condensed (J. Org. Chem. 2011, 76, 3511) the halide 5 with benzaldehyde and aqueous ammonia to give the imine 6. Young Hoon Jung of Sungkyunkwan University used (Tetrahedron Lett. 2011, 52, 1901) chlorosulfonyl i
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Lambert, Tristan H. "Functional Group Protection." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0014.

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Alfonso Iadonisi at the University of Naples Federico II developed (Eur. J. Org. Chem. 2013, 3137) a procedure for the selective acetolysis of the perbenzylated sugar 1 to furnish 3 using isopropenyl acetate (2) instead of the more typical and high-boiling acetic anhydride. The (3,4-dimethoxylphenyl)benzyl (DMPBn) protecting group, which is removed (cf. 4 → 5) under acidic conditions in the presence of the cation scavenger 5, was developed (J. Org. Chem. 2013, 78, 5264) by David S. Larsen at the University of Otago as an alternative to the p-methoxybenzyl (PMB) group. Another new hydroxyl-prot
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