Relevant bibliographies by topics / Benzal Derivatives

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

Academic literature on the topic 'Benzal Derivatives'

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

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Journal articles on the topic "Benzal Derivatives"

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Dekate, Shital M., Kishor M. Hatzade, and Ajay M. Ghatole. "A Facile Synthesis of Thiazole Derivatives bearing Imidazole Moiety, Schiff Bases and their O-Glucosides." Asian Journal of Chemistry 35, no. 1 (2022): 29–38. http://dx.doi.org/10.14233/ajchem.2023.24049.

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A unique approach for the synthesis of new thiazole O-glycosides is presented in this work. 2-Amino-4-hydroxy-phenyl-1,3-thiazole-5-carboxaldehyde (3a) was reacted with phenyl glyoxal and benzil to form 4-(4-hydroxy-phenyl)-5-(4-phenyl-1H-imidazol-2-yl)-thiazol-2-amine (4a) and 4-(4-hydroxy-phenyl)-5-(4,5-diphenyl-1H-imidazol-2-yl)-thiazol-2-amine (4b), respectively. A series of substituted Schiff bases of 4a and 4b were synthesized reacting with various aryl aldehyde to form 2-(imino substituted benzal)-4-(4-hydroxy-phenyl)-5-(4-phenyl-1H-imidazol-2-yl)-thiazoles (5a-e) and 2-(imino substitut
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Zonov, Yaroslav V., Siqi Wang, Vladislav V. Komarov, Victor M. Karpov, Dmitriy A. Parkhomenko, and Tatyana V. Mezhenkova. "Carbonylation of Polyfluorinated Alkylbenzenes and Benzocycloalkenes at the Benzyl C-F and C-Cl Bonds Under the Action of CO/SbF5." Molecules 30, no. 4 (2025): 931. https://doi.org/10.3390/molecules30040931.

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The carbonylation at the benzyl C-Hal bonds (Hal = F, Cl) of a number of polyfluorinated alkylbenzenes and benzocycloalkenes using carbon monoxide in the presence of SbF5 is described. The reaction provided the corresponding α-arylcarboxylic acids or their methyl esters following aqueous or methanol treatment. The products of double carbonylation were obtained from bis(chloromethyl)tetrafluorobenzenes and benzal fluorides. For benzal chloride derivatives, the possibility of selective mono- or dicarbonylation was shown to depend on the amount of antimony pentafluoride. In the case of polyfluori
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S., M. Mohamed, Khalile M., A. Ismail A., and S. Kadh M. "Synthesis and biological activity of some new pyrazole derivatives." Journal of Indian Chemical Society Vol. 82, Sep 2005 (2005): 833–37. https://doi.org/10.5281/zenodo.5827595.

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Chemistry Department, Faculty of Science (For Girls), Al-Azhar University, Nasr City, Egypt <em>Manuscript received 21 April 2004, revised 7 January 2005, accepted 20 June 2005</em> 1-Substituted-3-(2,4-dimethoxyphenyl)-5-(3,4,5-trimethoxyphenyl)-4,5-dihydropyrazoles were prepared via condensation or 3,4,5-(trimethoxy)benzal-2,4-(dimethoxy)acetophenone with hydrazine derivatives in ethanol and/or condensation with hydrazine hydrate in acidic medium. The product with ethyl iodide, phenyl isothiocyanate, benzoyl chloride and nitrous acid yielded the corresponding 1-substituted-3-(2,4-dimethoxyph
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Salwa Abdul Sattar Jabbar, Fawzi Hameed Jumaa, and Husniya Qadri Mawlood. "Synthesis and Characterization of some bis 1,3-Oxazepine and 2,3-Dihydroquinozoline derivatives." Tikrit Journal of Pure Science 20, no. 2 (2023): 110–20. http://dx.doi.org/10.25130/tjps.v20i2.1168.

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In this study some new compounds have been synthesized including preparation of some different Schiff bases[1-6] from the reaction benzdine with substituted of benzal-dehyde in absolute ethanol and converted into derivatives of 1,3-oxazpines(by ring clo- sure reaction (2+5) of Schiff bases with maleic anhydride in dry benzene[7-12],also the 2,3 –dihyroquinozoline-4(1H) one[13-17] were prepared. The prepared compounds were characterized by color and melting point determination, FT-IR and UV-Vis spectral analysis . Some of the prepared compounds were identified by 1H- NMR and C.H.N spectra analy
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Ran, deep Kaur Sandhar, R. Sharma J., and R. Manrao M. "Synthesis and fungitoxicity of aldimines and 4-thiazolidinones derived from 4-bromoaniline." Journal of Indian Chemical Society Vol. 85, Feb 2008 (2008): 220–23. https://doi.org/10.5281/zenodo.5808967.

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Department of Biochemistry and Chemistry, Punjab Agricultural University, Ludhiana-141 004, Punjab, India <em>Manuscript received 26 October 2005, revised 1 August 2007, accepted 26 November 2007</em> Condensation of 4-bromoaniline with benzaldehyde and substituted benzaldehydes (1-8) in equimolar ratio resulted in the formation of benzal-4-bromoaniline and its C-phenyl derivatives (la-8a). Addition of thioglycolic acid to la-8a yielded the respective 4-thiazolidinone (lb-8b). The synthesized compounds were characterized on the basis of elemental analysis and spectral studies and were screened
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SHIM, S. C., C. H. DOH, D. Y. LEE, et al. "ChemInform Abstract: Cobalt-Catalyzed Carbonylation of Benzal Chloride Derivatives to Alkyl Phenylacetates. Part 2." ChemInform 23, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.199222130.

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Y., M. ISSA, M. OMAR M, M. ABDEL-FATTAH H., and A. SOLIMAN A. "Spectroscopic Investigation of some Thio Schiff Bases." Journal of Indian Chemical Society Vol. 73, Jan 1996 (1996): 55–59. https://doi.org/10.5281/zenodo.5892203.

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Chemistry Depattment. Faculty of Science, Cairo University, Cairo, Egypt <em>Manuscript received 21 May 1993, revised 18 April 1994, accepted 27 May 1994</em> Schiff bases of 2-aminothiophenol with some benzaldehyde derivatives have been prepared. The effect of substitution at the benzal ring on the band positions of <sup>ʋ</sup>C=N and <sup>𝛿</sup>CH(CH=N) is investigated; the electron-withdrawing groups lower the frequency as a result of decreased electron density on the C=N linkage while electron-donating groups exert an opposite effect. Band assignment of the proper absorption band is made
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Sabaa, M. W., N. A. Mohamed, Kh D. Khalil, and A. A. Yassin. "Organic thermal stabilizers for rigid poly(vinyl chloride) II. Benzal thiobarbituric acid and some of its derivatives." Polymer Degradation and Stability 70, no. 2 (2000): 121–33. http://dx.doi.org/10.1016/s0141-3910(00)00098-7.

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Gökçe, Mehtap, Ahmet Geciken, Engin Yıldırım, and Ali Tosun. "Synthesis and Anticonvulsant Activity of 5-Chloro-2(3H)-benzoxazolinone-3-acetyl-2-(o/p-substituted benzal) hydrazone Derivatives." Arzneimittelforschung 58, no. 11 (2011): 537–42. http://dx.doi.org/10.1055/s-0031-1296554.

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Elhady, A. N. El-Sharabasy A. S. Kassab S. R. R. Soliman A. M. F. &. Ali A. A. E. "New anticorrosion and flame retardant coating compositions based on 4-amino triazole derivatives , their Schiffs' bases and epoxy varnish." International Journal of Applied Research 6, no. 1 (2020): 60–72. https://doi.org/10.5281/zenodo.4013369.

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In this study, some recently amino triazole derivatives mainly 4-amino-5-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-thione(I),4-((furan-2-yl-methylene)amino)-5-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-thione(II), 4-((4-nitrobenzyl- idene)amino)-5-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-thione (III),4-((4-(dimethylamino)benzylidene)amino)-5-phenyl-2,4-dihydro-3H-1,2,4-triazole-3-thione (IV), 5-phenyl-4-((3-phenyl-4-((3-phenylallylidene) amino)-2,4-dihydro-3H-1,2,4-triazole-3-thione(V),4-(((3-phenyl-5-thioxo-1,5-dihydro-4H-1,2,4-triazole-4yl)imino)methyl)benzal-&nbsp; dehyde(VI),and3-(((3-phenyl-5-thio
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Dissertations / Theses on the topic "Benzal Derivatives"

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Jaafar, Amani. "Synthèse, Caractérisation et Activité biologique des complexes à base de thiosemicarbazone." Thesis, Angers, 2017. http://www.theses.fr/2017ANGE0011/document.

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Le thiosemicarbazide et le 4-méthylthiosemicarbazide réagissent par condensation avec des dérivés benzaldéhyde pour donner des produits de type thiosemicarbazone pouvant jouer le rôle de ligands.Ces derniers peuvent conduire en milieu éthanolique à la formation de divers complexes en réagissant avec des sels métalliques comme les chlorures et/ou bromures de cuivre(II), de nickel(II), de zinc(II), de cobalt(II) et de cadmium(II). La structure de ces ligands et de leurs complexes a été déterminée par spectroscopie infrarouge, par des analyses élémentaires et par cristallographie. Les ligands se
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Lenihan, Brian David. "Generation of o-quinodimethanes from derivatives of trimethyl (o- ((p-tolylsulfonyl)methyl)benzyl)silane : a synthetic equivalent for the o-quinodimethant-[alpha], [alpha]- /." The Ohio State University, 1992. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487780393267272.

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Abou-Elkhair, Reham A. I. "Synthesis of anthraquinone derivatives and their conjugates with 2'-deoxynucleosides as new probes for electron transfer studies in DNA." unrestricted, 2008. http://etd.gsu.edu/theses/available/etd-07182008-154942/.

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Thesis (Ph. D.)--Georgia State University, 2008.<br>Title from file title page. Thomas L. Netzel, Dabney W. Dixon, committee co-chairs; David Boykin, Jerry Smith, committee members. Electronic text (250 p. : ill. (some col.)) : digital, PDF file. Description based on contents viewed Nov. 20, 2008. Includes bibliographical references.
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Pham, Van Tuyet. "The synthesis and reactions of chiral 1,3,2-oxazaphospholane derivations : kinetic and mechanistic studies of polyether omega-phase catalyzed reactions of potassium cyanide with benzyl bromide in non-polar, aprotic solvent toluene." Diss., Georgia Institute of Technology, 1987. http://hdl.handle.net/1853/27416.

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Chang, Ren-Chieh, and 張仁傑. "Design and Synthesis of Benzyl Caffeate Derivatives as JAK2 Inhibitors." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/96461041056529506594.

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碩士<br>國立陽明大學<br>生物藥學研究所<br>99<br>JAK (Janus kinase) is a cytokine-induced kinase that activates STAT (Signal Transducer and Activator of Transcription) on many kinds of physiological effect such as cell proliferation, differentiation, and angiogenesis. Literature has been shown that over-activated JAK2/STAT3 pathway leads to highly transcription of oncogenes in various cancers, including solid tumor (e.g., liver, breast) as well as hematological malignancies. A series of JAK2 inhibitors have been developed and some of the inhibitors have been tested in clinical trial. Therefore, development of
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Jůza, Radomír. "Příprava benzoylovaných derivátů cyklodextrinů." Master's thesis, 2017. http://www.nusl.cz/ntk/nusl-365317.

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This master thesis deals with the preparation of the cyclodextrin (CD) derivatives that are suitable for complexation of the electron-rich aromatic compounds such as helicenes. The basic skeleton of native CD was perbenzoylated in all positions 2, 3 and 6 in the first place. Then the nucleophilic attack of carboxylates of benzoic acids with electron- withdrawing groups (NO2) or electron-donating group (NH2) to per(6-deoxy-6-iodo)-CD derivatives were used to prepare the perbenzoylated CD derivatives in the postition 6. Binding constant was determined for the prepared benzoylated derivatives of
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Lo, mei ting, and 羅美婷. "Apoptosis induced by 1-benzyl carbazole-4-carboxaldehyde derivatives in human leukemia cell lines." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/90007866802222515218.

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碩士<br>中國醫藥學院<br>藥物化學研究所<br>89<br>Abstract Synthesized 1-benzyl carbazole-4-carboxaldehyde derivatives ( LCY ) examined for their growth inhibition effects in human leukemia cell lines. HL60, U937, and K562 cells were treated with these compounds for 24 hours and their proliferation was determined by the propidium iodide DNA staining method. A dose-dependent decrease in the cell proliferation rate was observed for all compounds. LCY-12 had the highest growth inhibitory, and its IC50 were 2.58, 0.77, and 19.49 μM for HL60, U937, and K562 cells, respectively. DAPI-stained cells revea
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Huang, Chun-Lung, and 黃俊龍. "Synthesis and biological activity of 1-benzyl-4-hydroxy-3-phenylquinolin-2(1H)-one derivatives." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/37426286995940238871.

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碩士<br>中國醫藥大學<br>藥物化學研究所碩士班<br>94<br>The dissertation is based on the structure of 4-hydroxy- quinolin-2-(1H)-ones. In order to synthesize a series of derivatives of 1-benzyl-4-hydroxy-3-phenylquinolin-2(1H)-one (26a-g, 27a-g, 28, 29), Using the Bheemashankar′s solution-phase combinatorial synthetic method. The starting material is methyl anthranilate (16) that is condensated with 4-substituted-benzaldehydes 17a-h to obtain the 19a-h. On the other hand, 4-cyanophenyl acetic acids 20a-d were acylated with thionyl chloride to afford acid chlorides 21a-d. Then, 21a-d and 19a-h are combined by Scho
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Yang, Ju-Ying, and 楊如盈. "Transformation of D-(-)-quinic acid into 3,4,6-trihydroxyazepanes and their N-benzyl derivatives for potential glycosidase inhibitors." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/00627216705643635736.

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碩士<br>淡江大學<br>化學學系碩士班<br>93<br>The naturally occurring five- and six-membered azasugars are considered as glycosidase inhibitors. Most recently, the seven-membered azasugars(poly-hydroxyazepanes) were reported to have potential in treatment of diabetes, cancers and AIDS. These heterocycles are more flexible in conformation than the corresponding six- and five-membered counterparts and may bind in the minor groove of DNA. Little attention has been given to trihydroxyazepanes. We wish to describe herein a new approach to the synthesis of diastereomeric azasugars (3,4,6-trihydroxyazepanes) in
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Tsai, Shang-Cheng, and 蔡尚宬. "I. Synthesis of D-amino acid derivatives from camphorII . Preparation of 1-benzyl indenones from 1-indanone." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/79a39r.

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碩士<br>國立暨南國際大學<br>應用化學系<br>107<br>I、Most of the natural amino acids are mainly L-amino acids, and the D-amino acids are the enantiomers of L-amino acids, which can be incorporated into the peptides to adjust their biological activities. In this laboratory, we used the camphor as the starting material for the Witting reaction, the oxidation reaction, the ring expansion reaction and the reduction reaction to obtain the organic catalyst based on camphor. On this basis, we used palladium metal as the catalyst after the hydrogenation expansion product. The hydrogenated product is obtained, and then
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Books on the topic "Benzal Derivatives"

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Dasgupta, Aparupa. A derivative generator: Bānglā morph computing : based on a morphological generator for Bangla : a study on Banglagen.vbp. Today & Tomorrow's Printers and Publishers, 2016.

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Book chapters on the topic "Benzal Derivatives"

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Delmau, Lætitia H., Jeffrey C. Bryan, Benjamin P. Hay, Nancy L. Engle, Richard A. Sachleben, and Bruce A. Moyer. "Benzyl Phenol Derivatives: Extraction Properties of Calixarene Fragments." In ACS Symposium Series. American Chemical Society, 2000. http://dx.doi.org/10.1021/bk-2000-0757.ch007.

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Yoshida, Masahito, Koya Saito, and Takayuki Doi. "Total Synthesis of (+)-Siladenoserinol A." In Modern Natural Product Synthesis. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-1619-7_4.

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AbstractThe total synthesis of (+)-siladenoserinol A (1) was accomplished. The bicyclic acetal core, a 6,8-dioxabicyclo[3.2.1]octane skeleton, was constructed by Au(III)-catalyzed cycloisomerization of 6,7-dihydroxy-2-alkynoate. A serinol side chain was introduced by the Julia–Kocienski olefination and the other side chain was efficiently introduced by the Horner–Wadsworth–Emmons reaction with glycerophosphocholine-containing phosphonoacetate, and selective sulfamation of the serinol moiety yielded (+)-1. The synthetic (+)-1 exhibited potent inhibitory activity against p53–Hdm2 interaction com
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Krause, Eberhard, Michael Beyermann, Rüdiger Winter, R. Haseloff, Ingolf E. Blasig, and Michael Bienert. "Studies on thioether modifications: S-oxidation, S-oxide reduction and regeneration of methionine peptides from their S-benzyl-sulfonium derivatives." In Peptides. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2264-1_184.

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Lv, Jian, Lei Lv, Xiaomin Zhang, et al. "Design, Synthesis and Biological Evaluation of the Novel Antitumor Agent 2-benzyl-3, 4-dihydroisoquinolin-1(2H)-one and Its Derivatives." In Proceedings of the 2012 International Conference on Applied Biotechnology (ICAB 2012). Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-37922-2_83.

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D. Adesina, Adebimpe. "The Chemistry of Benzo and Carbocyclic Derivatives of Pyridine." In Exploring Chemistry with Pyridine Derivatives [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.108127.

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The chemistry of pyridine and its derivatives is of considerable importance in the synthesis of intermediates leading to biologically active compounds and novel materials. Generally, derivatives of pyridine are stable and relatively unreactive but can be attacked by electrophiles at ring nitrogen and certain carbon atoms. Pyridines undergo radical substitution reactions preferentially at the 2-position. Simple pyridines and their benzo derivatives are weak bases that form salts with strong acids. Various Lewis acids form complexes with pyridine and its benzo derivatives. The quaternization of
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Ihmels, H. "Cyclization of 1-Benzyl-2-formylpyridinium Derivatives." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01589.

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Vashchenko, B. V., and O. O. Grygorenko. "37.9 Product Class 9: 1,4-Dioxanes." In Science of Synthesis: Knowledge Updates 2021/3. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-137-00104.

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AbstractIn this chapter, the synthesis of substituted 1,4-dioxanes and their saturated bridged, fused, and spirocyclic derivatives is discussed for the first time in Science of Synthesis. Partially unsaturated compounds, in particular benzo, 2-oxo, and related derivatives, are excluded from this review. Methods based on the construction of the 1,4-dioxane core, as well as on functionalization of the parent 1,4-dioxane and 2,3-dihydro-1,4-dioxine are presented.
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Jilal, Issam, Soufian El Barkany, Zahra Bahari, et al. "New Ethylenediamine Crosslinked 2D-Cellulose Adsorbent for Nanoencapsulation Removal of Pb (II) and Cu (II) Heavy Metal Ions: Synthesis, Characterization Application, and RSM-Modeling." In Cellulose Science and Derivatives. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.98709.

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The main objective of the present work is to elaborate on a new eco-friendly and efficient adsorbent designated for aquatic micropollutants removal. However, the synthesis of the Ethylenediamine Crosslinked 2D-Cellulose green adsorbent was carried out successfully, by partial grafting of benzyl entities onto hydroxyl groups of HEC, and crosslinking with ethylenediamine ED. Further, the new ethylenediamine crosslinked 2D-Cellulose was used as a biosorbent for nanoencapsulation removal of copper and lead heavy metal ions from aqueous solutions. The proposal chemical structures of unmodified and
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Aitken, R. A. "10.17 Benzo[b]phospholes." In Knowledge Updates 2022/2. Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/sos-sd-110-02138.

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AbstractThis chapter is a complete revision and update of the earlier Science of Synthesis contribution from 2000 describing methods for the synthesis of benzo[b]phospholes. About half of the references cited describe newer methods reported between 2000 and 2021 and, as well as extensions to the previously described approaches, several completely new approaches are included. Among the strategies covered are reactions of metalated phenylalkyne derivatives with phosphorus halides, cyclizations of (2-alkynylphenyl)phosphorus compounds, direct reactions of phenylphosphorus compounds with alkynes,
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Steriade, Donca, and Igor Yanovich. "Accentual Allomorphs in East Slavic: An Argument for Inflection Dependence." In Understanding Allomorphy: Perspectives from Optimality Theory. Equinox Publishing Ltd., 2015. http://dx.doi.org/10.1558/equinox.25220.

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This study analyzes a pattern of inflection dependence (Steriade 2008) in the distribution of accentual stem allomorphs in East Slavic, and it explores the significance of this pattern for the analysis of the phonological cycle. Inflected forms in Ukrainian and Russian surface with accented or unaccented stems as a predictable function of their inflectional class, the underlying accent of their root and further phonological factors. The result is that some lexemes possess multiple accentual stem allomorphs, others have invariably accented or invariably unaccented stems in inflection. We show t
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Conference papers on the topic "Benzal Derivatives"

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Yang, Zhen, Yefei Wang, Fengtao Zhan, et al. "Investigation of High-efficient Acidizing Inhibitors: Structure and Anti-corrosion Performance of Novel Indolizine Derivatives." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-12744.

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Abstract The novel indolizine derivative inhibitor for acidizing shows an effective corrosion inhibition without the synergism of propargyl alcohol. The inhibitive indolizine derivatives were generated from BQC (Benzyl Quinolinium Chloride, a commonly used key compound in acidizing inhibitor) via a moderate 1,3-dipolar cycloaddition mechanism. High Resolution Mass Spectrometry (HRMS) and NMR were used to confirm the detailed chemical structure. The inhibition of two indolizine derivatives in 15 wt.% HCl for N80 steel were studied by weight loss measurement and electrochemical analysis. Without
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Kopecky, Sarah E. "Investigation of Substituent Effects on the Corrosion Inhibition of Pyridine Derivatives with Acetylenic Alcohols on Steel in Acid Media." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05569.

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Abstract The corrosion inhibition of substituted pyridine derivatives and quaternized pyridines in the presence and absence of acetylenic alcohol synergists is reported. Electrochemical Frequency Modulation (EFM) was used as a method of monitoring corrosion rates of steel in acidic environments. Early stage pitting was evaluated via scanning electron microscope (SEM) for comparison of measured corrosion rates to observed pit formation. EFM was found to be a reliable and accurate method of monitoring general corrosion rates over time, and causality factor data was found to depend heavily on the
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Singh, Ambrish. "Corrosion Mitigation Properties of Xanthone Derivatives as Novel and Efficient Corrosion Inhibitors for P110 Steel in Acidizing Fluid: Experimental and Theoretical Studies." In LatinCORR 2023. AMPP, 2023. https://doi.org/10.5006/lac23-19928.

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Abstract Corrosion of metal during the acidizing process is destructive. The past research reveals the development of corrosion inhibitors that are effective only in lower acidic conditions. The present study aimed to fill the gap by the development of two xanthone derivatives, namely 12-(4-chlorophenyl)-9,9-dimethyl-8,9,10,12-tetrahydro-11H-benzo[a]xanthen-11-one (BX-Cl) and 9,9-dimethyl-12-(4-nitrophenyl)-8,9,10,12-tetrahydro-11H-benzo[a]xanthen-11-one (BX-NO2) using microwave irradiation techniques and well-characterized via IR, NMR, and MS for the corrosion inhibition of P110 steel in 15%
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May, Roger C., Longchun Cheng, and Feng Shao. "Second Generation, Halogen Resistant Copper Corrosion Inhibitors." In CORROSION 2002. NACE International, 2002. https://doi.org/10.5006/c2002-02413.

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Abstract Copper alloys are utilized in industrial cooling systems because of their excellent heat transfer properties. However, a corrosion inhibitor is needed to prevent equipment failures and, very importantly, to reduce the discharge of toxic copper compounds into the environment. Azoles, such as benzotriazole (BZT) and tolyltriazole (TTA), have been used for this purpose but they do not protect copper in the presence of oxidizing halogens which are commonly added to cooling systems to control microbiological activity. The halogens react with BZT and TTA and destroy their corrosion inhibiti
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Warsito, Warsito, Masruri Masruri, Sinta Murlistyarini, Dwika Putri Pangesti, and Asyfariatus Zulfa Azhar. "Screening Multitarget Anticancer Compounds from Salicylic Acid Derivatives: (Without and with Amino Acid Linkage) by <i>In Silico</i> Docking." In International Conference on Chemistry and Material Sciences 2023 (IC2MS). Trans Tech Publications Ltd, 2024. http://dx.doi.org/10.4028/p-svkm5p.

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This research aims to design anticancer molecules using the hybridization concept based on molecular derivatives of salicylic acid. The investigation explores structures with and without linked amino acid alanine through an in-silico docking approach. The research conducts screenings of the designed salicylic acid derivative molecules against receptors, including MMP9, MMP2, CDK2, P53, BAK EGFR, and ADP Ribose Polymerase. The most promising docking results for multitarget cancer compounds were observed in salicylic acid derivatives with amino acid linkages, specifically salicylic acid-curcumin
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Miller, Terry A. "Laser spectroscopy of aromatic and organometallic radicals." In OSA Annual Meeting. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/oam.1992.thi1.

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Laser induced fluorescence techniques can be used to obtain rotationally resolved electronic spectra of moderately large aromatic and organometallic radicals cooled to &lt;2 K in a supersonic free jet expansion. Aromatic organic radicals studied include cyclopentadienyl, benzyl, triphenyl methyl, and substituted derivatives thereof. Organometallic radicals studied include Cd and Zn monomethyl as well as group IIA and IIB derivatives of cyclopentadienyl, methylcyclopentadienyl, and pyrrolyl radicals.
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Hatem, Khalid Jamal, and Moayd N. Mohammed. "Synthesis of some new thioimidazolidine compound derivatives from benzil." In 2ND INTERNATIONAL CONFERENCE OF MATHEMATICS, APPLIED SCIENCES, INFORMATION AND COMMUNICATION TECHNOLOGY. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0164892.

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8

Zbancioc, Gheorghita, Costel Moldoveanu, and Ionel I. Mangalagiu. "Syntheses of new benzoquinoline derivatives with anticancer activity." In Conferința științifică națională cu participare internațională "Integrare prin cercetare și inovare", dedicată Zilei Internaționale a Științei pentru Pace și Dezvoltare. Moldova State University, 2025. https://doi.org/10.59295/spd2024n.92.

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This work synthesized various novel benzo[c]quinoline compounds, detailed their structural features, and examined their anticancer activity in vitro. First, the nitrogen atom in benzo[c]quinoline is quaternized, and the in situ-formed ylide is then subjected to a [3+2] dipolar cycloaddition reaction. A detailed investigation was conducted to determine how successful traditional thermal heating (TH) synthesis was in comparison to microwave (MW) and ultrasonic (US) irradiation. FTIR, HRMS, and NMR were the three spectral techniques that were used to prove the structure of all the obtained compou
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Nayak, Sudhanshu Kumar, Md Soif Ahmed, Someshwar Pola, et al. "Ultrafast Nonlinear Optical Studies of Polycyclic Aromatic Hydrocarbon (PAHs) based Benzo[b]naphtho[1,2,3,4-pqr] Perylene using Femtosecond Z-scan." In Frontiers in Optics. Optica Publishing Group, 2022. http://dx.doi.org/10.1364/fio.2022.jtu4b.15.

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The ultrafast nonlinear optical properties of Polycyclic aromatic hydrocarbon (PAHs) based benzo[b]perylene derivative named as benzo[b]naphtho[1,2,3,4-pqr]perylene (BNP) are studied using femtosecond Z-scan at 800 nm. A strong three-photon absorption coefficient of 0.56×10-5 cm3/GW2 was observed.
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Salimova, E. V., E. V. Tretyakova, and L. V. Parfenova. "Fischer reaction in the synthesis of indole derivatives of fusidic acid benzyl ester." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069131.

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