Relevant bibliographies by topics / Chromone derivatives

Contents

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

Academic literature on the topic 'Chromone derivatives'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Chromone derivatives"

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Talhi, Oualid, Norah Bennamane, Artur Silva, et al. "Catalyst-Free One-Pot Synthesis of Chromeno-Imidazo-Pyridinones by an Aza-Michael Addition/Rearrangement/Heterocyclization Tandem Reaction." Synlett 29, no. 11 (2018): 1437–40. http://dx.doi.org/10.1055/s-0037-1609684.

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A one-pot synthesis of a novel series of chromeno-imidazo-pyridinone derivatives from 3-[(2-hydroxyphenyl)-3-oxoprop-1-en-1-yl]chromones and ethane-1,2-diamine at room temperature under catalyst-free conditions has been successfully developed. This approach involves a tandem aza-Michael addition reaction, a chromone-to-chromanone rearrangement, and a heterocyclization sequence, leading to chromeno-imidazo-pyridinone polyheterocycles. The structure and absolute configurations of the new compounds were elucidated by a combination of 1D- and 2D-NMR analyses and single-crystal X-ray diffraction.
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Mrug, Galyna, and Mykhaylo Frasinyuk. "Advances in chemistry of chromone aminomethyl derivatives." French-Ukrainian Journal of Chemistry 3, no. 2 (2015): 21–39. http://dx.doi.org/10.17721/fujcv3i2p21-39.

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Chromones play an important role in the design and discovery of new pharmacologically active compounds. A large volume of reports dedicated to synthesis and study of properties of nitrogen-containing chromone derivatives show important role of chromone alkaloid-like compounds. The present review covers achievements in the field of synthesis of chromone aminomethyl derivatives as one of perspective scaffolds.
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Deharkar, Pravin, Shridhar Satpute, and Deepa Panhekar. "Synthetic Routes and Biological Activities of Chromone Scaffolds: An Overview." Asian Journal of Chemistry 35, no. 4 (2023): 771–93. http://dx.doi.org/10.14233/ajchem.2023.23442.

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The central backbones of natural assets and therapeutic medications are chromone and flavone. Utilizing such preferred chalcone analogs in drug research has shown a successful blueprint, yielding new hits/leads and fast optimization procedures. Chromone can create novel molecules with pharmacological promise, particularly in neurological, inflammatory, infectious diseases, cancer and diabetes. The current perspective focuses mainly on flavones and flavonoids of biological significance, such as chromon-4-one analogs, both synthetic and natural sources. Furthermore, because drug repurposing is n
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Gomes, Ligia R., John Nicolson Low, Fernando Cagide, Alexandra Gaspar, and Fernanda Borges. "A comparison of the structures of some 2- and 3-substituted chromone derivatives: a structural study on the importance of the secondary carboxamide backbone for the inhibitory activity of MAO-B." Acta Crystallographica Section E Crystallographic Communications 71, no. 11 (2015): 1270–77. http://dx.doi.org/10.1107/s2056989015017958.

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The crystal structures of the 3-substituted tertiary chromone carboxamide derivative, C17H13NO3,N-methyl-4-oxo-N-phenyl-4H-chromene-3-carboxamide (1), and the chromone carbonyl pyrrolidine derivatives, C14H13NO3, 3-(pyrrolidine-1-carbonyl)-4H-chromen-4-one (3) and 2-(pyrrolidine-1-carbonyl)-4H-chromen-4-one (4) have been determined. Their structural features are discussed and compared with similar compounds namely with respect to their MAO-B inhibitory activities. The chromone carboxamide presents a –synconformation with the aromatic rings twisted with respect to each other [the dihedral angle
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Lei, Jie, Yong Li, Liu-Jun He, et al. "Expeditious access of chromone analogues via a Michael addition-driven multicomponent reaction." Organic Chemistry Frontiers 7, no. 8 (2020): 987–92. http://dx.doi.org/10.1039/d0qo00145g.

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A Michael addition-driven four-component reaction (4-CR) with four Ugi inputs was developed and utilized for the synthesis of chromone derivatives and tetrazole substituted chromones under mild reaction conditions.
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Michalska, Marta, Wojciech Pajak, Justyna Kołodziejska, Andrzej Lazarenkow, and Jolanta Nawrot-Modranka. "Influence of phosphorohydrazone derivatives of benzopyrones on polymerization and viscosity of fibrin." Acta Biochimica Polonica 55, no. 3 (2008): 613–17. http://dx.doi.org/10.18388/abp.2008_3068.

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The synthesis and antitumour and antibacterial activity of coumarin and chromone phosphorohydrazones have been reported. This study describes influence of phosphorohydrazones derivatives of coumarin and chromone on the polymerization and viscosity of fibrin. The fibrin polymerization assay was performed by the Shen and Lorand method and the clot viscosity was measured on the basis of Shen and Lorand and Marchi and coworkers methods. Among the eight compounds tested, one coumarin derivative and two chromone derivatives showed significant activity.
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K., P. Swathi*1 Mary Mathew2 Gayathri3. "In-Silico Design, Synthesis and Antiprolifertive Evaluation of Thiazolidino-Chromone Derivatives." International Journal of Pharmaceutical Sciences 3, no. 3 (2025): 249–60. https://doi.org/10.5281/zenodo.14975982.

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Chromones are a group of naturally occurring chemical compound that being existing everywhere in nature, predominantly in plants. The word chromone is derived from the Greak word Chroma,which means colour, which bringing up that most of chromone derivatives can exhibit distinctiveness, in colour.Chromones are the oxygen containing heterocyclic compounds with a benzoannelated γ-Pyrone ring (4H-Chromone-4-one,4H-benzopyran-4-one). Now a days chromone act as a valid scaffold in medicinal chemistry. Our aim was to develop novel thizolidino- chromone derivatives which inhibiting Human Topo (I
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Sugiyama, Takuji, Yuji Narukawa, Shunsuke Shibata, Ryo Masui, and Fumiyuki Kiuchi. "New 2-(2-Phenylethyl)chromone Derivatives and Inhibitors of Phosphodiesterase (PDE) 3A from Agarwood." Natural Product Communications 11, no. 6 (2016): 1934578X1601100. http://dx.doi.org/10.1177/1934578x1601100624.

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The MeOH extract of agarwood showed inhibitory activity against phosphodiesterase (PDE) 3A. Fractionation of the extract led to the isolation of two new 2-(2-phenylethyl)chromones, 6,8-dihydroxy-2-[2-(4′-methoxyphenyl)ethyl]chromone (6), and 6,7-dihydroxy-2-(2-phenylethyl)chromone (8), together with six known compounds. All isolated compounds were tested for their PDE 3A inhibitory activity using fluorescence polarization method. Compound 7 showed PDE 3 A inhibitory activity with IC50 of 4.83 μM.
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Gomes, Ligia R., John Nicolson Low, Carlos Fernandes, Alexandra Gaspar, and Fernanda Borges. "Crystal structures of ethyl 6-(4-methylphenyl)-4-oxo-4H-chromene-2-carboxylate and ethyl 6-(4-fluorophenyl)-4-oxo-4H-chromene-2-carboxylate." Acta Crystallographica Section E Crystallographic Communications 72, no. 1 (2016): 8–13. http://dx.doi.org/10.1107/s2056989015022781.

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The crystal structures of two chromone derivatives,viz.ethyl 6-(4-methylphenyl)-4-oxo-4H-chromene-2-carboxylate, C19H16O4, (1), and ethyl 6-(4-fluorophenyl)-4-oxo-4H-chromene-2-carboxylate C18H13FO4, (2), have been determined: (1) crystallizes with two molecules in the asymmetric unit. A comparison of the dihedral angles beween the mean planes of the central chromone core with those of the substituents, an ethyl ester moiety at the 2-position and apara-substituted phenyl ring at the 6-position shows that each molecule differs significantly from the others, even the two independent molecules (a
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Tarasenko, Dmytro O., Andriy Y. Chumak, Oleksii O. Kolomoitsev, Volodymyr M. Kotliar, and Alexander D. Roshal. "Synthesis of a New Series of Chromones Based on Formylthiazoles." Journal of Organic and Pharmaceutical Chemistry 21, no. 4 (2023): 3–10. http://dx.doi.org/10.24959/ophcj.23.292844.

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A preparative approach to thiazole-containing chromone derivatives has been developed by modifying the corresponding aldehydes with their further transformation into propenone derivatives, and finally introducing them into the Algar-Flynn-Oyamada reaction. Several methods for obtaining propenones have been analyzed, and the most effective and practically convenient one has been found. The thiazole-containing analogs of chromones obtained have a great potential as probes for a wide range of studies.
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Dissertations / Theses on the topic "Chromone derivatives"

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Sabbagh, Liezel Veronica. "Chemical studies of chromone derivatives." Thesis, Rhodes University, 2001. http://hdl.handle.net/10962/d1006899.

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This study has focussed on several aspects of chromone chemistry, viz., (i) the influence of remote substituents on the basicity of 2-(N,N-dimethylamino)chromones, (ii) MoritaBaylis-Hillman reactions of substituted chromone-3-carbaldehydes and (iii) an investigation into the application of chromone chemistry in the total synthesis of the marine natural product, Rietone A. Selected 2-(N,N-dimethylamino )chromones were prepared using two different methods; firstly, via cyclisation of salicylate-derived N,N-dimethyl-3;.(2-hydroxyphenyl)-3- oxopropanamide precursors and, secondly, via 2-hydroxyace
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Nchinda, Aloysius Tchangwe. "Chemical studies of selected chromone derivatives." Thesis, Rhodes University, 2002. http://hdl.handle.net/10962/d1007442.

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This investigation has been geared towards several aspects of chromone chemistry. Selected 2-(N,N-dimethylarnino)chromones have been synthesized via 2-hydroxyacetophenone boron difluoride complex intermediates, and potentiometric analysis of these compounds in ethanolwater has been used to determine the influence of substituents on their basicity. The pKa values have been found to lie within a narrow range (1.92 - 2.52), and the observed substituent effects have been rationalized with the aid of semi-empirical and ab initio molecular orbital calculations. An efficient route has been developed
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Davidson, Deborah Nicole. "Chemical and spectroscopic studies of chromone derivatives." Thesis, Rhodes University, 1992. http://hdl.handle.net/10962/d1006857.

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Various chromone derivatives have been used in asthma therapy, and their biological activity is apparently related to certain chemical features which include conformation and acidity. In the present study, substituent effects on conformation and acidity have been explored in chromone systems with potential biological activity. A range of variously substituted symmetrical chromone-2-carboxamides (including a series of N,N-dimethylchromone-2-carboxamides) have been prepared via chromone-2-carboxylic acids, which, in turn, were prepared from the corresponding o-hydroxyacetophenones. The N,N-dimet
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Ramaite, Ipfani David Isaiah. "Chemical and spectroscopic studies of chromone derivatives." Thesis, Rhodes University, 1993. http://hdl.handle.net/10962/d1006888.

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A number of biologically active chromones occur in plants (eg. Khellin) and research in this field has eventually led to the discovery of chromoglycic acid, which is widely used as a sodium salt in asthma therapy. Since biological activity may be related to acidity, a range of chromone-2-carboxylic acids have been prepared via Claisen acylation of substituted o- hydroxyacetophenones and their acid dissociation constants determined potentiometrically to explore substituent effects. From this study it has been found that introduction of certain groups does have a marked effect on acidity. A vari
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Ramaite, Ipfani David Isaiah. "Synthetic and physical organic studies of chromone derivatives." Thesis, Rhodes University, 1997. http://hdl.handle.net/10962/d1005045.

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A range of chromone-2-carboxylic acids has been prepared by condensing suitably substituted 2-hydroxyacetophenones with diethyl oxalate. pK₂ Studies of these acids revealed that 6- or 7-methoxy substituents decreased acidity while the 6-nitro group enhanced acidity; the strongest acid was the 3-chloro derivative, the increase in acidity being attributed to steric inhibition of acid-weakening delocalisation between the carboxyl group and the chromone system. Various chromone-2-carboxamides, derived from acid chloride precursors, were converted to polysubstituted acrylamides by nucleophilic ring
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Molefe, Duduzile Mabel. "Studies directed towards the synthesis of chromone carbaldehyde-derived HIV-1 protease inhibitors." Thesis, Rhodes University, 2008. http://hdl.handle.net/10962/d1015542.

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A series of chromone-3-carbaldehydes have been prepared using Vilsmeier-Haack methodology while a corresponding series of chromone-2-carbaldeydes have been synthesized via the Kostanecki-Robinson reaction. Baylis-Hillman reactions have been conducted on both series of chromone carbaldehydes using three different catalysts, viz., 1,4-diazabicyclo(2.2.2]octane (DABCO), 1,8-diazabicyclo[5.4.0]undec- 7-ene (DBU) and 3-hydroxyquinuclidine (3HQ), and acrylonitrile, methyl acrylate and methyl vinyl ketone as the activated alkenes. These reactions have typically (but not always!) afforded both normal
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Mujahid, M. "Asymmetric syntheses of pharmaceutically important compounds employing hydrolytic kinetic resolution strategy and development of novel chromone based derivatives as potent antitubercular agents." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2013. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2196.

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Obah, kosso Anne. "Arylsélénation et sélénocyanation d'hétérocycles riches en électrons." Electronic Thesis or Diss., Aix-Marseille, 2019. http://www.theses.fr/2019AIXM0643.

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Ce travail s’inscrit dans la recherche et le développement de nouvelles méthodologies pour la synthèse de molécules portant un groupement sélénocyané ou arylsélanyle. Dans une première partie, le trisélénodicyanure (TSD) généré à partir du malononitrile et du dioxyde de sélénium a été utilisé pour la substitution électrophile d’hétérocycles riches en électrons tels que les imidazohétérocycles, les chromèn-4-ones et également pour l’ipso-sélénocyanation d’acides arylboroniques sans l’utilisation de métaux. Cette sélénocyanation permet d’accéder rapidement et de façon fiable aux dimères diséléni
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Shervington, L. A. "Studies on a new synthesis of chromans." Thesis, Bucks New University, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.380298.

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Nocanda, Xolani Wittleton. "Applications of Baylis-Idllman methodology in the synthesis of chromene derivatives." Thesis, Rhodes University, 2001. http://hdl.handle.net/10962/d1018257.

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The reaction of salicylaldehyde with various activated alkenes, viz., methyl vinyl ketone, ethyl vinyl ketone, phenyl vinyl sulfone, phenyl vinylsulfonate, acrolein and acrylonitrile, under Baylis-Hillman conditions, has been found to proceed with the chemoselective formation of chromene derivatives. The reaction conditions have been optimised and chromene derivatives have been obtained in isolated yields up to 87 %. The generality of the reaction, using 1,4-diazabicyclo[2.2.2]octane (DABCO), as the catalyst, and a heterogeneous (chloroform-water) solvent system, has been established using a r
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Book chapters on the topic "Chromone derivatives"

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Ellis, G. P. "Chromone and its Benzo Derivatives." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187012.ch10.

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Ellis, G. P. "Chromone Carbonitriles and Tetrazole Derivatives." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187012.ch18.

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Ellis, G. P. "Chromone Carboxylic Acids and Their Derivatives." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187012.ch20.

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Messere, R., A. F. Noels, P. Dournel, and J. Breulet. "Derivatives of Chromocene in Ethylene Polymerisation." In Metathesis Polymerization of Olefins and Polymerization of Alkynes. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5188-7_24.

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Ellis, G. P. "Chroman Carboxylic Acids and Their Derivatives." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187098.ch9.

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Avdović, Edina, Dušan Dimić, and Dejan Milenković. "Investigation of Coumarin Derivative 3-(1-o-toluidinoethylidene)-chromane-2,4-dione: IR Spectroscopic Characterization, NBO, and AIM Analysis and Molecular Docking Studies." In Learning and Analytics in Intelligent Systems. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-43658-2_12.

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Verma, Nitin, Parul Sood, Jitender Singh, Niraj Kumar Jha, Mahesh Rachamalla, and Kamal Dua. "Chromene and its Importance: Chemistry and Biology." In The Role of Chromenes in Drug Discovery and Development. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815124330123010003.

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Chromene (benzopyrans) is one of the privileged scaffold molecules that are widely distributed in natural products and possesses a wide variety of pharmacological activities such as anticoagulant, antioxidant, anti-inflammatory, anti-spasmolytic, antitumor, antihepatotoxic, diuretic, estrogenic, antiviral, antifungal, antimicrobial, anthelminthic, anti-HIV, antitubercular, herbicidal, anticonvulsant and analgesic. Their low toxicity combined with their broad pharmacological properties has inspired researchers to obtain new chromenes and derivatives possessing considerable pharmacological actio
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Bisht, Dheeraj, Deepak Sati, Rajeshwar Kamal Kant Arya, Amit Kumar Nigam, Monu Kumar Shukla, and Deepak Kumar. "The Implication of Chromene Derivatives in Bioactive Admixtures." In The Role of Chromenes in Drug Discovery and Development. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815124330123010013.

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Chromene is a heterocyclic scaffold and can be obtained from the natural origin (from different fractions of the plant extracts), synthetic origin as well as mineral origin. The nucleus of the scaffold possesses the ability to interact with different biological targets and thus is medicinally active. Chromene derivatives obtained from different origins are reported to possess pharmacological activities such as antitumor, antibacterial, anti-inflammatory, antithrombotic, and antipsychotic activities. Many chromene-based admixtures are reported to possess different bioactivities. Many derivative
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Bisht, Dheeraj, Aadesh Kumar, Ankit Kumar, Rajeshwar Kamal-Kant Arya, Krittika Mukherjee, and Mohmmad Rashid. "Role of Chromene in the Cure of Different Kinds of Human Disease." In The Role of Chromenes in Drug Discovery and Development. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815124330123010006.

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A variety of chemicals were being used by us for the treatment of human and animal diseases from the early beginning of civilization. These chemicals may be from a natural or synthetic source. Here the choice of discussion is being focused on the chemical name Chromene and its derivatives that have a significant effect on various health diseases of human beings. Over the past few years, various natural, as well as synthetic derivatives of chromene, have shown several fascinating features. These chromene derivatives were being used in the treatment of Alzheimer’s disease and Chagas disease. The
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Ruikar, Dipti B., Karan Joshi, Rasana Yadav, Gajanan J. Deshmukh, Snehal Manekar, and Prashant R. Murumkar. "Chromene and its Derivatives in the Treatment of SARS-COV- 2 Virus Infection." In The Role of Chromenes in Drug Discovery and Development. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815124330123010010.

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Coronavirus pandemics are characterizing the 21st century in itself. In 2002- 03, the first coronavirus SARS-CoV caused Severe Acute Respiratory Syndrome (SARS); in 2012, the Middle East Respiratory Syndrome (MERS-CoV) made its appearance, and in 2019, a new human beta coronavirus strain, the SARS-CoV-2 led to COVID-19 pandemic that took over the entire globe under its rollout. The scientific research and medical challenges to save lives have revealed the biochemistry and genetic evolution of an important cycle of the new pathogen, which has steered us to new preventive and therapeutic approac
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Conference papers on the topic "Chromone derivatives"

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Stojković, Danijela, Sandra Jovičić Milić, Dušica Simijonović, Edina Avdović, Tamara Mladenović, and Zoran Marković. "In Vitro and in Silico Binding Studies of Chromeno-Pyrimidine Derivatives With Biological Important Protein-Part III." In 2024 IEEE 24th International Conference on Bioinformatics and Bioengineering (BIBE). IEEE, 2024. https://doi.org/10.1109/bibe63649.2024.10820495.

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Dietsche, Frank, Thomas Heidenfelder, Helmut Witteler, and Keith Hirsch. "Organic Corrosion Inhibitors for Industrial Water Treatment." In CORROSION 2007. NACE International, 2007. https://doi.org/10.5006/c2007-07067.

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Abstract The use of corrosion inhibitors in formulas for boiler cleaning and for cooling water is well established but an increasing number of regulations and the abolishment of various well-tried corrosion inhibiting actives put up a new challenge. Chromate, molybdate, nitrite, phosphonate and other inhibitors are being abandoned for either ecotox or cost reasons. In this presentation, the potential of organic corrosion inhibitors for industrial water treatment is demonstrated. After a brief survey on structure and function of organic corrosion inhibitors, the function and the mechanisms of c
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Nikalje, Anna Pratima, Shailee Tiwari, Julio Seijas Vázquez, and M. Pilar Vazquez-Tato. "Ionic Liquid Mediated Synthesis Of Novel Chromone-Pyrimidine Coupled Derivatives." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04826.

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Simijonović, Dušica, Edina Avdović, Žiko Milanović, Dejan Milenković, and Zoran Marković. "Green synthesis of chromeno-pyrimidine derivatives – Part I." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.686s.

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Two different chromeno-pyrimidine derivatives were synthetized in the ionic liquid catalyzed reaction of barbituric acid and substituted salicylaldehydes. The product 5-(7-bromo-2,4-dioxo-1,3,4,5-tetrahydro-2H-chromeno[2,3-d]pyrimidin-5-yl)pyrimidine-2,4,6(1H,3H,5H)-tri-one (CP-1) was obtained in the reaction of barbiruric acid and 5-bromo-2-hydroxybenzaldehyde. The second new product 8,9-dihydroxy-2H-chromeno[2,3-d]pyrimidine-2,4(3H)-dione (CP-2) was yielded in the reaction between barbituric acid and 2,3,4-trihydroxybenzaldehyde. These products were isolated in moderate to good yield after 3
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Meshcheryakova, Anna A., Ekaterina A. Konstantinova, Karina A. Melkonyan, Alexandra A. Khrustaleva, and Vitaliy V. Sorokin. "The Synthesis of Various 2-Imino-2H-chromene-3-carbonitrile Derivatives." In ECSOC 2023. MDPI, 2023. http://dx.doi.org/10.3390/ecsoc-27-16125.

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Kobryn, Lesya, Jevgeniya Bila, Mykola Ganushchak, and Volodymyr Mizyuk. "Synthesis and Spectral Properties of Heterocycles as 2H-2-chromenone Derivatives." In The 8th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2004. http://dx.doi.org/10.3390/ecsoc-8-01940.

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Cortés, Iván, Andrea Bracca, and Teodoro Kaufman. "Short and efficient first total synthesis of the natural product chromanone A, a chromone derivative from the algicolous marine fungus <em>Penicillium</em> sp." In The 24th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08300.

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Stankovicová, Henrieta, Radoslav Flašík, Jana Donovalová, and Anton Gáplovský. "New 2H-chromen-2-one Derivatives Potentially Utilizable as Memory Media." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01210.

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Maleki, Ali, and Vahid Eskandarpour. "Cellulose@Fe2O3-SO3H: A Novel Magnetic Composite Nanomaterial for the Synthesis of Chromene Derivatives." In 1st International Electronic Conference on Materials. MDPI, 2014. http://dx.doi.org/10.3390/ecm-1-b004.

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Fiallos-Ayala, Ariana, Christian David Alcívar-León, Pablo M. Bonilla-Valladares, Juan Carlos Romero-Benavides, and Jorge Heredia-Moya. "Experimental and Theoretical Study of a New Functionalized Derivative of 3-Methyl-2-Trifluoromethyl Chromone." In ECSOC 2024. MDPI, 2024. https://doi.org/10.3390/ecsoc-28-20116.

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Reports on the topic "Chromone derivatives"

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Dumont, R., J. Potvin, and F. Kiss. First vertical derivative of the magnetic field, Jennings River aeromagnetic survey, British Columbia, Chromite Mountain 104 O/09, British Columbia. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2007. http://dx.doi.org/10.4095/223282.

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