المؤلفون: Donghuan Xu, Zhong Wang, Weibing Zhuang, Tao Wang, Yinfeng Xie

المصدر: Frontiers in Plant Science, Vol 14 (2023)

مصطلحات موضوعية: BAHD acyltransferase, protein structure, catalytic mechanism, phylogenetic reconstruction, acylation reactions, Plant culture, SB1-1110

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fpls.2023.1218914/fullTest; https://doaj.org/toc/1664-462XTest

الوصول الحر: https://doaj.org/article/2e05c9e8d1144b7aa98efc0d795e5324Test

المؤلفون: Kunling Liu, Mengmeng Fu, Xue Ma, Pengcheng Zhang, Shuai Zong, Wenjie Zhao

مصطلحات موضوعية: Biochemistry, Medicine, Ecology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, order dynamics model, linked microporous polymers, improve productive efficiency, causing ecological risk, aqueous solution despite, poor adsorption capacity, langmuir adsorption model, adsorption kinetics indicated, adsorption isotherms demonstrated, purpose reagent strategy, craft acylation reactions, including hydrophobic interactions, harsh synthesis conditions, rich pore structure, adsorbents commonly used, 371 mg g, efficiently removing mb, water methylene blue, 2 , methylene blue, maximum adsorption, adsorption process, adsorption performance, traditional adsorbents

العلاقة: https://figshare.com/articles/journal_contribution/One-Pot_Synthesis_of_Carboxyl-Functionalized_Hyper-Cross-Linked_Microporous_Polymer_Based_on_the_Dual-Purpose_Reagent_Strategy_for_the_Efficient_Removal_of_Methylene_Blue_from_Water/24560090Test

الإتاحة: https://doi.org/10.1021/acsapm.3c01529.s001Test
https://figshare.com/articles/journal_contribution/One-Pot_Synthesis_of_Carboxyl-Functionalized_Hyper-Cross-Linked_Microporous_Polymer_Based_on_the_Dual-Purpose_Reagent_Strategy_for_the_Efficient_Removal_of_Methylene_Blue_from_Water/24560090Test

المؤلفون: Dr. Zheng‐Wang Qu, Dr. Hui Zhu, Prof. Stefan Grimme

المصدر: ChemistryOpen, Vol 8, Iss 6, Pp 807-810 (2019)

مصطلحات موضوعية: acylphosphine, acylation reactions, reaction mechanism, norbornadienes, phosphenium, Chemistry, QD1-999

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2191-1363Test

الوصول الحر: https://doaj.org/article/1e658d9316ae4929a9f2c93a42028379Test

المؤلفون: Ivan A. Yaremenko (2030395), Yulia Yu. Belyakova (5042789), Peter S. Radulov (5042786), Roman A. Novikov (1532962), Michael G. Medvedev (3589598), Nikolai V. Krivoshchapov (9234734), Alexander A. Korlyukov (1549351), Igor V. Alabugin (1267017), Alexander O. Terent’ev (1392754)

مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Molecular Biology, Physiology, Evolutionary Biology, Immunology, Inorganic Chemistry, Infectious Diseases, Computational Biology, Chemical Sciences not elsewhere classified, ammonium salts, hydrogen peroxide, electron density, Nitrogen Heterocycles, chemical stability, NH moiety, amine alkylation, 15 p K, 1 year, bicyclic stereochemically, acylation reactions, interaction, peroxide group, Unusual Stability, Bridged Azaozonides Stable bridged ., Peroxide-Preserving Rearrangement, catalyst-free three-component conde., aminoperoxide rearrangement, gram quantities

العلاقة: https://figshare.com/articles/journal_contribution/Marriage_of_Peroxides_and_Nitrogen_Heterocycles_Selective_Three-Component_Assembly_Peroxide-Preserving_Rearrangement_and_Stereoelectronic_Source_of_Unusual_Stability_of_Bridged_Azaozonides/14456237Test

الإتاحة: https://doi.org/10.1021/jacs.1c02249.s001Test

المؤلفون: Mittersteiner, Mateus, Machado, Tayani M., Jesus, Paulo Cesar de, Brondani, Patrícia B., Scharf, Dilamara R., Wendhausen Jr., Renato

المصدر: Journal of the Brazilian Chemical Society. July 2017 28(7)

مصطلحات موضوعية: lipases, immobilization, silica gel, enzymatic resolution, acylation reactions

وصف الملف: text/html

الوصول الحر: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017000701185Test

المؤلفون: Luna-Mora,Ricardo Alfredo, Ortega-Jiménez,Fernando, Ríos-Guerra,Hulme, García-Estrada,José Guadalupe, Pérez-Flores,Francisco Javier, González-Carrillo,Jessica, Torres-Reyes,Ángeles, Moreno-González,Linda, Martínez-Zaldivar,Alejandro, Penieres-Carrillo,José Guillermo

المصدر: Journal of the Mexican Chemical Society v.63 n.2 2019

مصطلحات موضوعية: Acylation reactions, Green chemistry, simultaneous infrared-ultrasound irradiation (SIUI)

وصف الملف: text/html

الإتاحة: http://www.scielo.org.mx/scielo.php?script=sci_arttext&pid=S1870-249X2019000200071Test

المؤلفون: Mohammad I. M. Al-Zeer, Kenneth J. D. MacKenzie

المصدر: Catalysts; Volume 9; Issue 4; Pages: 372

مصطلحات موضوعية: fly ash-based geopolymer, heterogeneous catalysis, sustainability, redox catalysts, acylation reactions

وصف الملف: application/pdf

العلاقة: https://dx.doi.org/10.3390/catal9040372Test

الإتاحة: https://doi.org/10.3390/catal9040372Test

المؤلفون: Adailton J. Bortoluzzi, Damianni Sebrão, Marcus M. Sá, Cho Mr, Mo K Radiation

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/e0/44/Acta_Crystallogr_Sect_E_Struct_Rep_Online_2011_Sep_30_67(Pt_10)_o2778.tar.gz

مصطلحات موضوعية: acylation reactions, see, Díaz-Rodríguez et al. (2005, Wu et al

وصف الملف: application/zip

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.349.9539Test

المؤلفون: Бучкевич, І. Р., Хом`як, С. В., Курка, М. С., Федоришин, О. М., Марінцова, Н. Г., Buchkevych, I. R., Khomyak, S. V., Kurka, M. S., Fedoryshyn, O. M., Marintsova, N. G.

المساهمون: Національний університет “Львівська політехніка”

مصطلحات موضوعية: 4-нафтохінон, реакції алкілювання та ацилювання, сульфініл-хлорид, сульфонілхлорид, 4-naphthoquinone, alkylation and acylation reactions, sulfinyl chloride, sulfonyl chloride

جغرافية الموضوع: Lviv

الوقت: 1

وصف الملف: 88-97; application/pdf; image/png

العلاقة: Chemistry, Technology and Application of Substances, 2 (1), 2018; http://www.way2drug.com/PASSTest; 1. F. Giroud, R. Milton, B. Tan, et al. Simplifying Enzymatic Biofuel Cells: Immobilized Naphthoquinone as a Biocathodic Orientational Moiety and Bioanodic Electron Mediator // ACS Catal. – 2015, 5, P. 1240–1244.; 2. V. Tandon, D. Yadav, R. Singh, et al. Synthesis and biological evaluation of novel (L)-α-amino acid methyl ester, heteroalkyl, and aryl substituted 1,4-naphthoquinone derivatives as antifungal and antibacterial agents // Bioorg. Med. Chem. Letters – 2005. – No. 15. – P. 5324–5328.; 3. S. Sandur, H. Ichikawa, G. Sethi et al. Plumbagin (5-Hydroxy-2-methyl-1,4-naphthoquinone) Suppresses NF-B Activation and NF-kB-regulated Gene Products Through Modulation of p65 and IkBα Kinase Activation, Leading to Potentiation of Apoptosis Induced by Cytokine and Chemotherapeutic Agents // J. Biological Chemistry – 2006. – No. 25. – Vol. 281. – P. 17023–17033.; 4. Fries K., Pense W., Peters O. Uber lin Benzo-p-thiazino-chinone // Ber. – 1928. – No. 61. – P. 1395–1401.; 5. Бучкевич І. Р., Платонов М. О., Стасевич М. В., Лубенець В. І., Мусянович Р. Я. Синтез нових азотовмісних похідних 2,3,6- трихлор-1,4-нафтохінону // Вісник Національного університету „Львівська політехніка” Хімія, технологія речовин та їх застосування. – 2009. – № 644. – С. 111–114.; 6. Шишкина Р. П., Маматюк В. П., Фокин Е. И. Сульфирование и сульфохлорирование 2,3-дихлор-1,4-нафтохинона. // Изв. Сиб. Отд. АН СССР. Сер. Химия. – 1984. – № 3. – C. 855–857.; 7. Pingaew R., Prachayasittikul V., Worachartcheewan A. et al. Novel 1,4-naphthoquinone-based sulfonamides: synthesis, QSAR, anticancer and antimalarial studies / Euro. J.Med. Chem. – 2015. – No. 103. – P. 446–459.; 8. Buchkevych I., Stasevych M., Musyanovych R. et al. S- and N,S-Containing heterocycles based on sulfenyl chlorides of substituted 1,4-naphthoquinone // Chemistry of Heterocyclic Compounds. – 2010. – Vol. 46(4). – P. 502–504.; 9. Satheshkumar A., Elango K. Spectroscopic and theoretical studies on the nucleophilic substitution of 2,3-dichloronaphthoquinone with para-substituted anilines in solid state via initial charge transfer complexation // Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. – 2012. – Vol. 98. – P. 378–383.; 11. Bolibrukh K., Polovkovych S., Khoumeri O. et al. Synthesis and anti-platelet activity of thiosulfonate derivatives containing a quinone moiety // Scientia Pharmaceutica. – 2015. – Vol. 83 (2). – P. 221–231.; 12. PASS (Prediction of Activity Spectra for Substances) [електронний ресурс] / режим доступу до ресурсу: http://www.way2drug.com/PASSTest Online/.; 1. F. Giroud, R. Milton, B. Tan, et al. Simplifying Enzymatic Biofuel Cells: Immobilized Naphthoquinone as a Biocathodic Orientational Moiety and Bioanodic Electron Mediator, ACS Catal, 2015, 5, P. 1240–1244.; 2. V. Tandon, D. Yadav, R. Singh, et al. Synthesis and biological evaluation of novel (L)-α-amino acid methyl ester, heteroalkyl, and aryl substituted 1,4-naphthoquinone derivatives as antifungal and antibacterial agents, Bioorg. Med. Chem. Letters – 2005, No. 15, P. 5324–5328.; 3. S. Sandur, H. Ichikawa, G. Sethi et al. Plumbagin (5-Hydroxy-2-methyl-1,4-naphthoquinone) Suppresses NF-B Activation and NF-kB-regulated Gene Products Through Modulation of p65 and IkBα Kinase Activation, Leading to Potentiation of Apoptosis Induced by Cytokine and Chemotherapeutic Agents, J. Biological Chemistry – 2006, No. 25, Vol. 281, P. 17023–17033.; 4. Fries K., Pense W., Peters O. Uber lin Benzo-p-thiazino-chinone, Ber, 1928, No. 61, P. 1395–1401.; 5. Buchkevych I. R., Platonov M. O., Stasevych M. V., Lubenets V. I., Musianovych R. Ya. Syntez novykh azotovmisnykh pokhidnykh 2,3,6- trykhlor-1,4-naftokhinonu, Visnyk Natsionalnoho universytetu "Lvivska politekhnika" Khimiia, tekhnolohiia rechovyn ta yikh zastosuvannia, 2009, No 644, P. 111–114.; 6. Shishkina R. P., Mamatiuk V. P., Fokin E. I. Sulfirovanie i sulfokhlorirovanie 2,3-dikhlor-1,4-naftokhinona., Izv. Sib. Otd. AN SSSR. Ser. Khimiia, 1984, No 3, P. 855–857.; 7. Pingaew R., Prachayasittikul V., Worachartcheewan A. et al. Novel 1,4-naphthoquinone-based sulfonamides: synthesis, QSAR, anticancer and antimalarial studies, Euro. J.Med. Chem, 2015, No. 103, P. 446–459.; 8. Buchkevych I., Stasevych M., Musyanovych R. et al. S- and N,S-Containing heterocycles based on sulfenyl chlorides of substituted 1,4-naphthoquinone, Chemistry of Heterocyclic Compounds, 2010, Vol. 46(4), P. 502–504.; 9. Satheshkumar A., Elango K. Spectroscopic and theoretical studies on the nucleophilic substitution of 2,3-dichloronaphthoquinone with para-substituted anilines in solid state via initial charge transfer complexation, Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012, Vol. 98, P. 378–383.; 11. Bolibrukh K., Polovkovych S., Khoumeri O. et al. Synthesis and anti-platelet activity of thiosulfonate derivatives containing a quinone moiety, Scientia Pharmaceutica, 2015, Vol. 83 (2), P. 221–231.; 12. PASS (Prediction of Activity Spectra for Substances) [Electronic resource], Access mode: http://www.way2drug.com/PASSTest Online/.; Дослідження реакційної здатності аміногрупи в 2-, 6- та 7- положеннях 1,4-нафтохінону / І. Р. Бучкевич, С. В. Хом`як, М. С. Курка, О. М. Федоришин, Н. Г. Марінцова // Chemistry, Technology and Application of Substances. — Lviv : Lviv Politechnic Publishing House, 2018. — Том 1. — № 2. — С. 88–97.; https://ena.lpnu.ua/handle/ntb/46337Test; Studies of reactivity of amino group in the 2-, 6-, 7- position of 1,4-naphthoquinone / I. R. Buchkevych, S. V. Khomyak, M. S. Kurka, O. M. Fedoryshyn, N. G. Marintsova // Chemistry, Technology and Application of Substances. — Lviv : Lviv Politechnic Publishing House, 2018. — Vol 1. — No 2. — P. 88–97.

الإتاحة: https://ena.lpnu.ua/handle/ntb/46337Test

المصدر: SciTech Book News. Jun2010, Vol. 34 Issue 2, p39-43. 5p.

مصطلحات موضوعية: *NONFICTION

Reviews & Products: FORENSIC Applications of High Performance Liquid Chromatography (Book), ADVANCES in Friedel-Crafts Acylation Reactions: Catalytic & Green Processes (Book), MICROSCALE Organic Laboratory With Multistep & Multiscale Syntheses (Book)

People: BAYNE, Shirley, CARLIN, Michelle, SARTORI, Giovanni, MAGGI, Raimondo, MAYO, Dana