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Journal articles on the topic 'Substituted benzophenone'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Cox, Philip J., Dimitrios Kechagias, and Orla Kelly. "Conformations of substituted benzophenones." Acta Crystallographica Section B Structural Science 64, no. 2 (2008): 206–16. http://dx.doi.org/10.1107/s0108768108000232.

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The inclination of the two aryl rings (ring twists) in a series of benzophenone molecules has been examined. For each structure the dihedral angle (between the planes of the two sets of six aromatic C atoms) relates to both the steric considerations of the single molecule and the packing forces related to the crystal structure. Six new benzophenone structures are incorporated into the study including 2,2′-dihydroxy-4,4′-dimethoxybenzophenone (I), C15H14O5, that appears to have the smallest reported twist angle, 37.85 (5)°, of any substituted benzophenone reported to date. Three further benzoph

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2

Samarov, Artemiy A., Stanislav O. Kondratev, and Sergey P. Verevkin. "Nearest-Neighbour and Non-Nearest-Neighbour Non-Covalent Interactions between Substituents in the Aromatic Systems: Experimental and Theoretical Investigation of Functionally Substituted Benzophenones." Molecules 27, no. 23 (2022): 8477. http://dx.doi.org/10.3390/molecules27238477.

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Benzophenone derivatives exhibit not only biological activity but also act as photo initiator and UV blocker. We carried out experimental and theoretical thermochemical studies of hydroxy- and methoxy-substituted benzophenones. Standard molar enthalpies of vaporisation were obtained from the temperature dependence of vapour pressures measured by the transpiration method. The thermodynamic data on phase transitions available in the literature (crystal–gas, crystal–liquid, and liquid–gas) were also collected and evaluated. High-level quantum chemical methods G3MP2 and G4 were used to estimate th

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3

VIDYA, JOSHI, та K. SHARMA R. "Diazotisation Rearrangement of Tosylhydrazones of ortho- and meta-Substituted-benzophenones and α-Substituted-acetophenones (Synthesis of Anilides)". Journal of Indian Chemical Society Vol. 65, Aug 1988 (1988): 564–66. https://doi.org/10.5281/zenodo.6042085.

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Institute of Science, 15, Madam Cama Road, Bombay-400 032 <em>Manuscript received 25 January 1988, accepted 28 May 2988</em> <em>Ortho</em>- and <em>meta</em>-substituted-benzophenones (1a —g) and substituted-acetophenones (1h — i) were converted into tosylhydrazones (2a— i) by reacting with<em> p</em>-toluenesulphonylhydrazide. Conversion of 2a — i to the anilides (3a —i) was effected with the reagents H<sub>2</sub>SO<sub>4</sub> and NaNO<sub>2</sub>, and was found to be as facile as In case of the <em>para</em>-substitutedbenzophenone hydrazones.

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4

Chung, Mee-Kyung, Paul Fancy, and Jeffrey M. Stryker. "Bis(ether) derivatives of tetrakis(2-hydroxyphenyl)ethene — Direct synthesis of (E)- and (Z)-bis(2-hydroxyphenyl)-bis(2-methoxyphenyl)ethene via the McMurry olefination reaction." Canadian Journal of Chemistry 84, no. 10 (2006): 1250–53. http://dx.doi.org/10.1139/v06-087.

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The direct synthesis of sterically hindered, partially etherified derivatives of tetrakis(2-hydroxyphenyl)ethene is reported by using the McMurry reductive olefination reaction on a range of differentially substituted 2,2′-dialkoxy benzophenone substrates. Three orthogonal protection strategies are demonstrated, incorporating β-silylethyl, 3-butenyl, and tert-butyl protecting groups, respectively, into the starting benzophenones. The latter proved most efficient, with both the McMurry coupling and deprotection steps occurring concomitantly under the McMurry conditions to directly yield the des

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5

Liu, Zhaoming, Haibo Tan, Kai Chen, et al. "Rhizophols A and B, antioxidant and axially chiral benzophenones from the endophytic fungus Cytospora rhizophorae." Organic & Biomolecular Chemistry 17, no. 47 (2019): 10009–12. http://dx.doi.org/10.1039/c9ob02282a.

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6

Bushra Begum, A., Noor Fatima Khanum, V. Lakshmi Ranganatha, T. Prashanth, Mohammed Al-Ghorbani, and Shaukath Ara Khanum. "Evaluation of Benzophenone-N-ethyl Morpholine Ethers as Antibacterial and Antifungal Activities." Journal of Chemistry 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/941074.

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Microorganisms are closely associated with the health and welfare of human beings. Whereas some microorganisms are beneficial, others are detrimental. Bacterial infections often produce inflammation and pains and in some instances, infections result in high mortality. Any subtle change in the drug molecule, which may not be detected by chemical methods, can be revealed by a change in the antimicrobial activity and hence microbiological assays are very useful. A series of substituted hydroxy benzophenones and benzophenone-N-ethyl morpholine ethers were screened for their antibacterial and antif

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7

Lange, Margaret J., Anna R. Oller, and Somnath Sarkar. "Antimicrobial Activity of Mono- and Di-Methyl Substituted Benzhydrols and Benzophenones In Vitro." Transactions of the Missouri Academy of Science 41, no. 2007 (2007): 14–19. http://dx.doi.org/10.30956/0544-540x-41.2007.14.

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Twelve compounds of mono methyl and symmetrical dimethyl substituted benzhydrol and benzophenone were synthesized using standard synthetic procedures and screened for possible antimicrobial activity against thirteen known Gram-positive and Gram-negative bacteria, as well as two yeasts. Most benzhydrol and benzophenone derivatives under investigation demonstrated some antimicrobial activity, with ortho-methylbenzophenone, dapsone, meta-dimethylbenzophenone, and para-dimethylbenzyhydrol showing the greatest inhibition. Only four compounds, ortho-methylbenzhydrol, para-methylbenzhydrol, para-meth

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8

R., A. KULKARNI, and R. THAKER S. "2-Benzoyl-4-substituted-phenyl-5-phenylthiazoles." Journal of Indian Chemical Society Vol. 65, Jun 1988 (1988): 427–28. https://doi.org/10.5281/zenodo.6298979.

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C. C. Shroff  Research Institute, Goregaon (W), Bombay-400 062 <em>Manuscript  received 7 January 1987, accepted 12 April 1988</em> Preparations of some 2-benzoyl-4-substituted-phenyl-5-phenylthiazoles are described.

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9

Jirman, Josef, та Alexander Popkov. "1H, 13C, and 15N NMR Spectra of Ni(II) Complexes of Schiff Bases of (S)-2-(N-Benzylprolyl)aminobenzophenone and α-Monosubstituted Glycine and Determination of Configuration of the Complexes by 2D NOESY Spectra". Collection of Czechoslovak Chemical Communications 60, № 6 (1995): 990–98. http://dx.doi.org/10.1135/cccc19950990.

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1H, 13C, and 15N NMR spectra have been measured of substituted Ni(II) complexes of Schiff bases of (S)-2-(N-benzylprolyl)aminobenzophenone and glycine. The absolute configuration at C19 of the substituted glycine can be determined from 2D NOESY spectra using the NOESY interactions with the proton of the second chiral centre of the complex. It is possible to determine the rate of rotation of phenyl group of benzophenone unless its rotation is prevented by requatorialr orientation of dimethylamino group as it is the case with the Ni(II) complex of Schiff base of (S)-2-(N-benzylprolyl)aminobenzop

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10

Rusanov, Alexander L., Ludmila G. Komarova, Marina P. Prigozhina, Roman S. Begunov, and Yulia S. Yakovleva. "Benzophenone-Type Unsymmetrical Substituted Aromatic Diamines and Organosoluble Polyimides Therefrom." High Performance Polymers 21, no. 6 (2008): 729–43. http://dx.doi.org/10.1177/0954008308099187.

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11

Khadilkar, Bhushan M., and Dharita J. Upadhyaya. "STUDIES IN BECKMANN REARRANGEMENT OF SUBSTITUTED BENZOPHENONE AND ACETOPHENONE OXIMES." Synthetic Communications 32, no. 12 (2002): 1867–73. http://dx.doi.org/10.1081/scc-120004081.

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12

Basarić, Nikola, Devin Mitchell, and Peter Wan. "Substituent effects in the intramolecular photoredox reactions of benzophenones in aqueous solution." Canadian Journal of Chemistry 85, no. 9 (2007): 561–71. http://dx.doi.org/10.1139/v07-081.

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A number of α-hydroxy-3-benzylbenzophenones 7–11 have been synthesized for the purpose of studying the effect of a phenyl substituent on the intramolecular photoredox reaction of 3-(hydroxymethyl)benzophenone (5) discovered in our laboratory. This latter compound was found to undergo a unimolecular (formal) intramolecular redox reaction upon photolysis in aqueous acid that results in clean reduction of the benzophenone ketone (to secondary alcohol) and oxidation of the alcohol to aldehyde. Three of the phenyl-substituted compounds with simple phenyl (7), p-methylphenyl (8), and p-methoxyphenyl

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13

Ghosh, Chandra Kanta, Sumit Kumar Karak та Amarendra Patra. "Benzopyrans. Part 43.1 Reactions of Some Simple Condensates of 4-oxo-4H-1-Benzopyran-3-Carboxaldehyde with Ethyl β-Aminocrotonate". Journal of Chemical Research 2002, № 7 (2002): 311–13. http://dx.doi.org/10.3184/030823402103172275.

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With ethyl β-aminocrotonate, the chromone 2A (X = H(A), Me(B), Cl(C)) gives a mixture of the dihydropyridine 4A and pyranopyridine 15A, 2B gives 4B, and 2C gives varying amounts of the substituted enamine 3C, pyridone 4C and benzophenone 8. 5-Hydroxy-5H-[1]benzopyrano-[4,3-b]pyridine 11 (< 3%) was obtained in each case. Palladised charcoal dehydrogenates dihydropyridines 4A and 4B to respectively 12A and 12B and ammonia converts 12A into the diazanaphthalene 13.

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14

Ahad, Faiza, Nida Ghouri, Khalid Mohammed Khan, Shahnaz Perveen, and M. Iqbal Choudhary. "Synthesis of 4-substituted ethers of benzophenone and their antileishmanial activities." Royal Society Open Science 5, no. 5 (2018): 171771. http://dx.doi.org/10.1098/rsos.171771.

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Leishmaniasis is a vector-borne protozoan disease; it mainly originates from the bite of sandfly and initiated when parasite is transmitted to human at metacyclic flagellated promastigote form. In the current study, a synthesis of a series of 4-substituted benzophenone ethers 1–20 was carried out in good yields and their in vitro antileishmanial activities were also screened. Among synthetic derivatives, 15 compounds 1 , 3 , 5–12 , 15 and 17 – 20 showed antileishmanial activities against promastigotes of Leishmania major with IC 50 values in the range of 1.19–82.30 µg ml −1 , and the values we

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15

Keruckiene, Rasa, Jonas Keruckas, Eglė Jatautiene, Jurate Simokaitiene, Dmytro Volyniuk, and Juozas Vidas Grazulevicius. "Synthesis and properties of tetrahidrocarbazolyl- and 2-phenylindolyl-substituted benzophenone derivatives." Journal of Photochemistry and Photobiology A: Chemistry 359 (May 2018): 157–63. http://dx.doi.org/10.1016/j.jphotochem.2018.04.010.

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16

García, C. Murcia, A. Espinosa Ferao, G. Schnakenburg, and R. Streubel. "CPh3 as a functional group in P-heterocyclic chemistry: elimination of HCPh3 in the reaction of P-CPh3 substituted Li/Cl phosphinidenoid complexes with Ph2CO." Dalton Transactions 45, no. 6 (2016): 2378–85. http://dx.doi.org/10.1039/c5dt04595a.

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17

Hu, Qintao, Pu Zhang, Yunpeng Zhang, and Jingwei Sun. "Polarity- and Pressure-Induced Emission from a Benzophenone-Based Luminophore." Molecules 27, no. 24 (2022): 8748. http://dx.doi.org/10.3390/molecules27248748.

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Since strong polarity usually causes emission quenching, materials with polarity-induced emission (PIE) are rarely reported despite their important applications in polar environments. Herein, an N-phenylcarbazole-substituted benzophenone derivative (BP-3-Cz) with a twisted electron donor–acceptor (D–A) structure is synthesized. The incorporation of heteroatoms into the twisted π-conjugated D–A backbone simultaneously endows BP-3-Cz with obvious polarity- and pressure-induced emission. Spectral analysis, X-ray diffraction, differential scanning calorimetry, and quantum chemical calculation resu

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18

Kim, Duck-Hyun, and A.-Young Sung. "Application of hydroxy-substituted benzophenone group for UV-block soft contact lens." Korean Journal of Vision Science 17, no. 1 (2015): 57–68. http://dx.doi.org/10.17337/jmbi.2015.17.1.57.

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19

Hou, Guohua, Ran Tao, Yongkui Sun, Xumu Zhang, and Francis Gosselin. "Iridium−Monodentate Phosphoramidite-Catalyzed Asymmetric Hydrogenation of Substituted Benzophenone N−H Imines." Journal of the American Chemical Society 132, no. 7 (2010): 2124–25. http://dx.doi.org/10.1021/ja909583s.

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20

Toyota, Shinji, Mitsuhiro Asakura, and Tatsuya Sakaue. "Intramolecular C=O···B Interactions ino-Boron Substituted Benzaldehyde, Acetophenone, and Benzophenone." Bulletin of the Chemical Society of Japan 75, no. 12 (2002): 2667–71. http://dx.doi.org/10.1246/bcsj.75.2667.

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21

Khadilkar, Bhushan M., and Dharita J. Upadhyaya. "ChemInform Abstract: Studies in Beckmann Rearrangement of Substituted Benzophenone and Acetophenone Oximes." ChemInform 33, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.200244054.

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22

M., M. Patel, A. Kapadia M., and D. Joshi J. "Applications of polychelates of 4-substituted benzophenone based resins with 'd' and 'f block elements." Journal of Indian Chemical Society Vol. 85, Dec 2008 (2008): 1239–47. https://doi.org/10.5281/zenodo.5819414.

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Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar-388 120, Gujarat, India <em>E-mail</em> : jdjoshi314@gmail.com <em>Manuscript received 8 September 2008, accepted I October 2008</em>  

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23

Xu, Jian-Lin, Hong-Xin Liu, Yu-Chan Chen, et al. "Highly Substituted Benzophenone Aldehydes and Eremophilane Derivatives from the Deep-Sea Derived Fungus Phomopsis lithocarpus FS508." Marine Drugs 16, no. 9 (2018): 329. http://dx.doi.org/10.3390/md16090329.

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Five new benzophenone derivatives named tenellones D–H (1–5), sharing a rare naturally occurring aldehyde functionality in this family, and a new eremophilane derivative named lithocarin A (7), together with two known compounds (6 and 8), were isolated from the deep marine sediment-derived fungus Phomopsis lithocarpus FS508. All of the structures for these new compounds were fully characterized and established on the basis of extensive spectroscopic interpretation and X-ray crystallographic analysis. Compound 5 exhibited cytotoxic activity against HepG-2 and A549 cell lines with IC50 values of

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24

Journal, Baghdad Science. "Synthesis of substituted (oxazepine, Diazepine, tetrazde) via Schiff Bases for 2- Aminobenzo Thaizole Derivatives." Baghdad Science Journal 10, no. 3 (2013): 736–48. http://dx.doi.org/10.21123/bsj.10.3.736-748.

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This work includs synthesis of several Schiff bases by condensation of 6- methoxy – 2- amino benzothiazole with some aldehydes and ketones (2- hydroxyl benzaldehyde, 4- hydroxyl benzaldehyde, 4- N,N –dimethy amino acetophenone, benzophenone) to abtain schiff bases (1-5). These schiff bases were found to react with phthalate anhydride to give oxazepine derivatives (6-10) that were reacted with primary aromatic amines to give Diazepine derivatives (11-15). Besides, we prepared new tetrazole derivatives (16-20) from the reaction of the prepared Schiff bases with sodium azide in the prepared compo

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25

Scott Sawyer, J., Ronald F. Baldwin, Larry L. Froelich, David L. Saussy, and William T. Jackson. "Synthesis and pharmacologic activity of hydroxyacetophenone-substituted benzophenone/xanthone leukotriene B4 receptor antagonists." Bioorganic & Medicinal Chemistry Letters 3, no. 10 (1993): 1981–84. http://dx.doi.org/10.1016/s0960-894x(01)80999-9.

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26

Lehmann, Thomas E., and Albrecht Berkessel. "Stereoselective Synthesis of 4‘-Benzophenone-Substituted Nucleoside Analogs: Photoactive Models for Ribonucleotide Reductases†." Journal of Organic Chemistry 62, no. 2 (1997): 302–9. http://dx.doi.org/10.1021/jo961372m.

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27

Hishmat, O. H., O. A. El-Shabrawy, S. S. Nakkady, and S. S. Mahmoud. "Synthesis and biological effects of 2,3-diphenyl-5-methoxyindole and substituted benzophenone derivatives." Archives of Pharmacal Research 12, no. 3 (1989): 149–53. http://dx.doi.org/10.1007/bf02855546.

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28

Nguyen, Thao P., and Richard Horn. "Movement and Crevices Around a Sodium Channel S3 Segment." Journal of General Physiology 120, no. 3 (2002): 419–36. http://dx.doi.org/10.1085/jgp.20028636.

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Voltage sensing is due mainly to the movement of positively charged S4 segments through the membrane electric field during changes of membrane potential. The roles of other transmembrane segments are under study. The S3 segment of domain 4 (D4/S3) in the sodium channel Nav1.4 carries two negatively charged residues and has been implicated in voltage-dependent gating. We substituted cysteines into nine putative “high impact” sites along the complete length of D4/S3 and evaluated their accessibilities to extracellular sulfhydryl reagents. Only the four outermost substituted cysteines (L1433C, L1

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29

Wu, Ze-Ling, Xin Lv, Ling-Yi Meng, Xu-Lin Chen, and Can-Zhong Lu. "Tröger’s Base-Derived Thermally Activated Delayed Fluorescence Dopant for Efficient Deep-Blue Organic Light-Emitting Diodes." Molecules 28, no. 12 (2023): 4832. http://dx.doi.org/10.3390/molecules28124832.

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The development of efficient deep-blue emitters with thermally activated delayed fluorescence (TADF) properties is a highly significant but challenging task in the field of organic light-emitting diode (OLED) applications. Herein, we report the design and synthesis of two new 4,10-dimethyl-6H,12H-5,11-methanodibenzo[b,f][1,5]diazocine (TB)-derived TADF emitters, TB-BP-DMAC and TB-DMAC, which feature distinct benzophenone (BP)-derived acceptors but share the same dimethylacridin (DMAC) donors. Our comparative study reveals that the amide acceptor in TB-DMAC exhibits a significantly weaker elect

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30

Güveli, Şükriye. "Nickel(II)-PPh3 complexes of substituted benzophenone thiosemicarbazones: Electrochemistry, structural analysis, and antioxidant properties." Journal of Coordination Chemistry 73, no. 1 (2020): 137–53. http://dx.doi.org/10.1080/00958972.2020.1711888.

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31

Nakatani, Kazuhiko, Chikara Dohno, Takashi Nakamura, and Isao Saito. "p -Cyano substituted benzophenone as an excellent photophore for one-electron oxidation of DNA." Tetrahedron Letters 39, no. 18 (1998): 2779–82. http://dx.doi.org/10.1016/s0040-4039(98)00337-2.

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32

Hou, Guohua, Ran Tao, Yongkui Sun, Xumu Zhang, and Francis Gosselin. "ChemInform Abstract: Iridium-Monodentate Phosphoramidite-Catalyzed Asymmetric Hydrogenation of Substituted Benzophenone N-H Imines." ChemInform 41, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.201029102.

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33

Andronati, S. A., Yu A. Simonov, V. I. Pavlovskii, O. V. Kulikov, M. Gdanec, and A. V. Mazepa. "Reaction of 5-Substituted 2-(3-Chloropropanoylamino)benzophenone syn- and anti-Oximes with Sodium Hydroxide." Russian Journal of General Chemistry 75, no. 6 (2005): 915–22. http://dx.doi.org/10.1007/s11176-005-0345-4.

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34

LEHMANN, T. E., and A. BERKESSEL. "ChemInform Abstract: Stereoselective Synthesis of 4′-Benzophenone-Substituted Nucleoside Analogues: Photoactive Models for Ribonucleotide Reductases." ChemInform 28, no. 20 (2010): no. http://dx.doi.org/10.1002/chin.199720201.

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35

Ito, Yoshikatsu, Yoshitaka Kusunaga, Kenichi Tabata, Hitoshi Arai, Ji-Ben Meng, and Teruo Matsuura. "Oxetane formation by addition of N-substituted imidazoles to benzophenone and poly(4-vinylbenzophenone)s." Journal of Applied Polymer Science 50, no. 11 (1993): 1989–98. http://dx.doi.org/10.1002/app.1993.070501117.

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36

Dwivedi, Bhavna, and Dinabandhu Das. "Polymorphism in some new bis-hydrazone compounds." Acta Crystallographica Section C Structural Chemistry 74, no. 12 (2018): 1656–66. http://dx.doi.org/10.1107/s2053229618014286.

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We describe the polymorphism of four new bis-hydrazone compounds, namely butane-2,3-dione 2,3-bis{[bis(4-fluorophenyl)methylidene]hydrazone}, C30H22F4N4 (1), butane-2,3-dione 2,3-bis{[bis(4-chlorophenyl)methylidene]hydrazone}, C30H22Cl4N4 (2), butane-2,3-dione 2,3-bis{[bis(4-methylphenyl)methylidene]hydrazone}, C34H34N4 (3), and butane-2,3-dione 2,3-bis({bis[4-(dimethylamino)phenyl]methylidene}hydrazone), C38H46N8 (4), derived by the condensation reaction between substituted benzophenone hydrazone and butane-2,3-dione. Concomitant polymorphism has been observed in 1, 2 and 3. Overlays of molec

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37

Smith, Keith, Gamal A. El-Hiti, Mohamed F. Abdel-Megeed, and Mohamed A. Abdo. "Convenient Synthesis of More Complex 2-Substituted 4(3H)-Quinazolinones via Lithiation of 2-Alkyl-4(3H)-quinazolinones." Collection of Czechoslovak Chemical Communications 64, no. 3 (1999): 515–26. http://dx.doi.org/10.1135/cccc19990515.

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2-Methylquinazolin-4(3H)-one has been doubly lithiated, at nitrogen and in the 2-methyl group, with n-butylithium. The lithium reagent thus obtained reacts with a variety of electrophiles (iodomethane, D2O, phenyl isocyanate, benzaldehyde, benzophenone, cyclopentanone, 2-butanone, carvone) to give the corresponding 2-substituted derivatives in very good yields. Reaction of the dilithio reagent with acetonitrile gives an α,β-unsaturated imine by tautomerization of the initial addition product. Double lithiation of 2-ethyl- and 2-propyl-4(3H)-quinazolinones can be achieved using lithium diisopro

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38

Zou, Ge, Taobo Li, Wencong Yang, et al. "Antioxidative Indenone and Benzophenone Derivatives from the Mangrove-Derived Fungus Cytospora heveae NSHSJ-2." Marine Drugs 21, no. 3 (2023): 181. http://dx.doi.org/10.3390/md21030181.

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Seven new polyketides, including four indenone derivatives, cytoindenones A–C (1, 3–4), 3′-methoxycytoindenone A (2), a benzophenone derivative, cytorhizophin J (6), and a pair of tetralone enantiomers, (±)-4,6-dihydroxy-5-methoxy-α-tetralone (7), together with a known compound (5) were obtained from the endophytic fungus Cytospora heveae NSHSJ-2 isolated from the fresh stem of the mangrove plant Sonneratia caseolaris. Compound 3 represented the first natural indenone monomer substituted by two benzene moieties at C-2 and C-3. Their structures were determined by the analysis of 1D and 2D NMR,

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39

Ibeji, C. U., J. Adegboyega, O. D. Okagu, and B. B. Adeleke. "Nature of Ground State of Benzophenone and some of its Substituted Derivatives: Experimental and DFT Study." Journal of Applied Sciences 16, no. 11 (2016): 504–16. http://dx.doi.org/10.3923/jas.2016.504.516.

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40

Subbaraj, P., A. Ramu, N. Raman, and J. Dharmaraja. "Synthesis, characterization, DNA interaction and pharmacological studies of substituted benzophenone derived Schiff base metal(II) complexes." Journal of Saudi Chemical Society 19, no. 2 (2015): 207–16. http://dx.doi.org/10.1016/j.jscs.2014.05.002.

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41

Kaiser, Florian, Lothar Schwink, Janna Velder, and Hans-Günther Schmalz. "Studies towards the total synthesis of mumbaistatin: synthesis of highly substituted benzophenone and anthraquinone building blocks." Tetrahedron 59, no. 18 (2003): 3201–17. http://dx.doi.org/10.1016/s0040-4020(03)00427-7.

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42

El-Asmy, A. A., and G. A. A. Al-Hazmi. "Synthesis and spectral feature of benzophenone-substituted thiosemicarbazones and their Ni(II) and Cu(II) complexes." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 71, no. 5 (2009): 1885–90. http://dx.doi.org/10.1016/j.saa.2008.07.005.

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43

Allen, N. S., W. Chen, F. Catalina, P. N. Green, and A. Green. "Photochemistry of novel water-soluble para-substituted benzophenone photoinitiators: A polymerization, spectroscopic and flash photolysis study." Journal of Photochemistry and Photobiology A: Chemistry 44, no. 3 (1988): 349–60. http://dx.doi.org/10.1016/1010-6030(88)80105-9.

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Kpoviessi, Bénédicta Kpadonou, Bardieu Atchadé, Basile Goueti, et al. "Synthesis, Spectrometrical Characterization and Pharmacological Properties of Six Substituted Hydrazones with Carbonyl Compounds." Chemical Science International Journal 34, no. 2 (2025): 11–24. https://doi.org/10.9734/csji/2025/v34i2953.

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Hydrazones are molecules that prevent the growth of several microbial and parasitic strains by inhibited the replication of DNA sequences due to their chelating properties of metal ions. They are well recognized for Antiparasitic, Antimicrobial, Antibacterial, Antiviral, Antitumoral, Antimalarial and Anticonvulsive activities. The aim of the current study is to synthesized novel substituted hydrazones of ketones and aromatic aldehydes and to study their antiparasitic activities against Trypanosoma brucei brucei parasite. Synthesized hydrazone derivatives have been confirmed by elemental analys

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Lathioor, Edward C., та William J. Leigh. "Geometric and solvent effects on intramolecular phenolic hydrogen abstraction by carbonyl n,π* and π,π* triplets". Canadian Journal of Chemistry 79, № 12 (2001): 1851–63. http://dx.doi.org/10.1139/v01-167.

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The photochemistry of a series of alkoxyacetophenone, -benzophenone, and -indanone derivatives, which contain a remote phenolic group linked to the ketone by a para,para'- or meta,meta'-oxyethyl spacer, has been studied in acetonitrile and dichloromethane solutions using laser flash photolysis techniques. The corresponding methoxy-substituted compounds and, in the case of the alkoxyindanones, derivatives bearing just a remote phenyl substituent, have also been examined. The triplet lifetimes of the phenolic compounds are determined by the rates of intramolecular abstraction of the remote pheno

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Tanaka, Chiho, Yoko Nambu, and Takeshi Endo. "Charge-transfer complexation and photoreduction of viologen derivatives bearing the para-substituted benzophenone group in dimethyl sulfoxide." Journal of Physical Chemistry 96, no. 17 (1992): 7018–21. http://dx.doi.org/10.1021/j100196a032.

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Yamada, Koji, Masaru Sato, Kenta Tanaka, Azusa Wakabayashi, Tetsutaro Igarashi, and Tadamitsu Sakurai. "Nitrile-forming radical elimination reactions of 1-naphthaldehyde O-(4-substituted benzoyl)oximes activated by triplet benzophenone." Journal of Photochemistry and Photobiology A: Chemistry 183, no. 1-2 (2006): 205–11. http://dx.doi.org/10.1016/j.jphotochem.2006.03.019.

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Blassan, Samuel, Pathak Madhvesh, and Jin Kim Kap. "Synthesis and characterization of new heteroleptic derivatives of titanium(IV) derived from 2-hydroxy-4-methoxy-benzophenone : A new precursors for the synthesis of nano sized titania." Journal of Indian Chemical Society Vol. 92, May 2015 (2015): 780–83. https://doi.org/10.5281/zenodo.5704112.

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Materials Chemistry Division, School of Advanced Sciences, VIT University, Vellore-632 014, Tamilnadu, India <em>E-mail</em> : madhveshpathak@vit.ac.in Department of Advanced Materials Engineering for Information and Electronics, College of Engineering, Kyung Hee University, 1732, Deogyeong-daero, Giheung-gu, Yongin-si, Gyeonggi-do 446-701, South Korea <em>E-mail</em> : kjkim@khu.ac.kr A few new titanium(IV) complexes have been synthesized by the reaction among precursor (Bp)<sub>2</sub>Ti(OPr<sup>i</sup>)<sub>2</sub> with different alkoxyalkanols and phenols/substituted phenols in 1 : 1 : 1 m

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Cai, Xichen, Masanori Sakamoto, Minoru Yamaji, Mamoru Fujitsuka, and Tetsuro Majima. "C−O Bond Cleavage of Benzophenone Substituted by 4-CH2OR (R= C6H5and CH3) with Stepwise Two-Photon Excitation." Journal of Physical Chemistry A 109, no. 27 (2005): 5989–94. http://dx.doi.org/10.1021/jp051703b.

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Vinaya, Mallappanahally, Hanuma Raja Naika, Channapille Ananda Kumar, et al. "Synthesis of Medicinally Important N-Trimethylene Dipiperidine Sulfonamides and Carboxamides Containing a Substituted Benzophenone Moiety - An Antibacterial Agents." Letters in Drug Design & Discovery 5, no. 4 (2008): 250–60. http://dx.doi.org/10.2174/157018008784619951.

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