Статті в журналах з теми "Peracid"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Peracid".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Patil, Vilas Venunath, and Ganapati Subray Shankarling. "Nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione." Beilstein Journal of Organic Chemistry 10 (April 24, 2014): 921–28. http://dx.doi.org/10.3762/bjoc.10.90.
Повний текст джерелаPikh, Zoryan. "Oxidation of unsaturated aldehydes by different oxidants." Chemistry & Chemical Technology 1, no. 2 (June 15, 2007): 61–69. http://dx.doi.org/10.23939/chcht01.02.061.
Повний текст джерелаArmstrong, Alan, Paul A. Barsanti, Paul A. Clarke, and Anthony Wood. "Ketone-directed peracid epoxidation." Tetrahedron Letters 35, no. 33 (August 1994): 6155–58. http://dx.doi.org/10.1016/0040-4039(94)88103-0.
Повний текст джерелаMinning, Stefan, Albrecht Weiss, Uwe T. Bornscheuer, and Rolf D. Schmid. "Determination of peracid and putative enzymatic peracid formation by an easy colorimetric assay." Analytica Chimica Acta 378, no. 1-3 (January 1999): 293–98. http://dx.doi.org/10.1016/s0003-2670(98)00612-6.
Повний текст джерелаBouzid, Mouna, Hassen Ben Salah, and Majed Kammoun. "Peracid Oxidation of Dihydroisoquinoline Iminium." Asian Journal of Organic and Medicinal Chemistry 3, no. 3 (2018): 121–25. http://dx.doi.org/10.14233/ajomc.2018.ajomc-p148.
Повний текст джерелаHassan, Suriaya, Abdul Ansari, Arvind Kumar, Munna Ram, Sulaxna Sharma, and Awanish Sharma. "Corrosion Resistance of Electroless Ni-P-W/ZrO<sub>2</sub> Nanocomposite Coatings in Peracid Solutions." Materials Science Forum 1048 (January 4, 2022): 72–79. http://dx.doi.org/10.4028/www.scientific.net/msf.1048.72.
Повний текст джерелаBuggle, Katherine, and Bernadette Fallon. "Peracid oxidation of benzothiopyranthiones and benzopyranthiones." Monatshefte f�r Chemie Chemical Monthly 118, no. 10 (October 1987): 1197–99. http://dx.doi.org/10.1007/bf00811293.
Повний текст джерелаARMSTRONG, A., P. A. BARSANTI, P. A. CLARKE, and A. WOOD. "ChemInform Abstract: Ketone-Directed Peracid Epoxidation." ChemInform 26, no. 1 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199501079.
Повний текст джерелаKim, Kwang-Seo, Jeffrey G. Pelton, William B. Inwood, Ulla Andersen, Sydney Kustu, and David E. Wemmer. "The Rut Pathway for Pyrimidine Degradation: Novel Chemistry and Toxicity Problems." Journal of Bacteriology 192, no. 16 (April 16, 2010): 4089–102. http://dx.doi.org/10.1128/jb.00201-10.
Повний текст джерелаParbat, Papiya, Alka Devi, and Vikas D. Ghule. "Computational assessment of nitrogen-rich peracids: a family of peroxide-based energetic materials." RSC Advances 7, no. 35 (2017): 21585–91. http://dx.doi.org/10.1039/c7ra02201h.
Повний текст джерелаArmstrong, Alan, Paul A. Barsanti, Paul A. Clarke, and Anthony Wood. "Ketone-directed peracid epoxidation of cyclic alkenes." Journal of the Chemical Society, Perkin Transactions 1, no. 12 (1996): 1373. http://dx.doi.org/10.1039/p19960001373.
Повний текст джерелаGINGERICH, S. B., and P. W. JENNINGS. "ChemInform Abstract: Peracid Oxidations of Furan Systems." ChemInform 22, no. 6 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199106328.
Повний текст джерелаBroggini, Gianluigi, and Gaetano Zecchi. "Peracid oxidation of chiral isoxazolidines: developments and perspectives." Tetrahedron: Asymmetry 8, no. 9 (May 1997): 1431–34. http://dx.doi.org/10.1016/s0957-4166(97)00098-0.
Повний текст джерелаMello, Rossella, Ana Alcalde-Aragonés, María Elena González Núñez, and Gregorio Asensio. "Epoxidation of Olefins with a Silica-Supported Peracid." Journal of Organic Chemistry 77, no. 15 (July 26, 2012): 6409–13. http://dx.doi.org/10.1021/jo300533b.
Повний текст джерелаCox, M., G. Klass, S. Morey, and P. Pigou. "Chemical markers from the peracid oxidation of isosafrole." Forensic Science International 179, no. 1 (July 2008): 44–53. http://dx.doi.org/10.1016/j.forsciint.2008.04.009.
Повний текст джерелаHsiue, Ging-Ho, Tirng-Lair Perng, and Jen-Ming Yang. "New peracid-type polymeric initiator for radical polymerization." Journal of Applied Polymer Science 42, no. 7 (April 5, 1991): 1899–904. http://dx.doi.org/10.1002/app.1991.070420712.
Повний текст джерелаAitken, R. Alan, Fiona M. Fotherby, and Alexandra M. Z. Slawin. "2,6-exo-8,10-exo-4-Butyl-9-oxa-4-azatetracyclo[5.3.1.02,6.08,10]undecane-3,5-dione." Molbank 2022, no. 1 (January 20, 2022): M1320. http://dx.doi.org/10.3390/m1320.
Повний текст джерелаZHANG, GUODONG, LI MA, VANESSA H. PHELAN, and MICHAEL P. DOYLE. "Efficacy of Antimicrobial Agents in Lettuce Leaf Processing Water for Control of Escherichia coli O157:H7." Journal of Food Protection 72, no. 7 (July 1, 2009): 1392–97. http://dx.doi.org/10.4315/0362-028x-72.7.1392.
Повний текст джерелаHaras, Alicja, and Tom Ziegler. "DFT mechanistic studies on the epoxidation of cyclohexene by non-heme tetraaza manganese complexes." Canadian Journal of Chemistry 87, no. 1 (January 1, 2009): 33–38. http://dx.doi.org/10.1139/v08-065.
Повний текст джерелаFATEMI, PAYMAN, and JOSEPH F. FRANK. "Inactivation of Listeria monocytogenes/Pseudomonas Biofilms by Peracid Sanitizers." Journal of Food Protection 62, no. 7 (July 1, 1999): 761–65. http://dx.doi.org/10.4315/0362-028x-62.7.761.
Повний текст джерелаMakitra, R. G., G. G. Midyana, and R. E. Pristanskii. "Solvent effects on the decomposition kinetics of peracid esters." Russian Journal of General Chemistry 78, no. 7 (July 2008): 1418–21. http://dx.doi.org/10.1134/s1070363208070232.
Повний текст джерелаAli, Sk Asrof, and Mohammed I. M. Wazeer. "Peracid induced ring opening of isoxazolidines. A mechanistic study." Tetrahedron Letters 33, no. 22 (May 1992): 3219–22. http://dx.doi.org/10.1016/s0040-4039(00)79856-x.
Повний текст джерелаBlack, DS, and RJ Strauch. "Nitrones and Oxaziridines. XL. Oxidation of 2H-Pyrroles and 3-Benzoyloxy-1-pyrrolines." Australian Journal of Chemistry 42, no. 5 (1989): 699. http://dx.doi.org/10.1071/ch9890699.
Повний текст джерелаBinder, W. H., and F. M. Menger. "Assay of Peracid in the Presence of Excess Hydrogen Peroxide." Analytical Letters 33, no. 3 (January 2000): 479–88. http://dx.doi.org/10.1080/00032710008543067.
Повний текст джерелаManfredi, K. P., and P. W. Jennings. "Effect of acid on the peracid oxidations of 3-methyltetrahydrobenzofuran." Journal of Organic Chemistry 54, no. 21 (October 1989): 5186–88. http://dx.doi.org/10.1021/jo00282a044.
Повний текст джерелаTokushige, N., Y. Yamaguchi, and Y. Hanada. "Bleaching detergent compositions containing hydrogen peroxide and organic peracid precursors." Zeolites 18, no. 1 (January 1997): 86. http://dx.doi.org/10.1016/s0144-2449(97)85006-3.
Повний текст джерелаBragd, P. "Selective oxidation of carbohydrates by 4-AcNH-TEMPO/peracid systems." Carbohydrate Polymers 49, no. 4 (September 1, 2002): 397–406. http://dx.doi.org/10.1016/s0144-8617(01)00344-7.
Повний текст джерелаMcElroy, Andrew B., та Stuart Warren. "Stereoselective peracid epoxidation of allylic and δ-hydroxyallylic diphenylphosphine oxides". Tetrahedron Letters 26, № 17 (1985): 2119–22. http://dx.doi.org/10.1016/s0040-4039(00)94795-6.
Повний текст джерелаWu, Shao-Yung, Robert F. Toia, and John E. Casida. "Mechanism of phosphinyloxysulfonate formation on peracid oxidation of ,,′ ,′-tetrasubstituted phosphorodiamidothiolates." Tetrahedron Letters 32, no. 35 (January 1991): 4427–30. http://dx.doi.org/10.1016/0040-4039(91)80003-o.
Повний текст джерелаFujise, Yutaka, Kenshu Fujiwara та Yukiko Ito. "Baeyer–Villiger Oxidation of β-Ionone with Surfactant Type Peracid". Chemistry Letters 17, № 9 (5 вересня 1988): 1475–76. http://dx.doi.org/10.1246/cl.1988.1475.
Повний текст джерелаBROGGINI, G., and G. ZECCHI. "ChemInform Abstract: Peracid Oxidation of Chiral Isoxazolidines: Developments and Perspectives." ChemInform 28, no. 39 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199739150.
Повний текст джерелаMello, Rossella, Ana Alcalde-Aragones, Maria Elena Gonzalez Nunez, and Gregorio Asensio. "ChemInform Abstract: Epoxidation of Olefins with a Silica-Supported Peracid." ChemInform 43, no. 51 (December 10, 2012): no. http://dx.doi.org/10.1002/chin.201251099.
Повний текст джерелаHofmann, Hans, and Herbert Fischer. "Heterocyclische Siebenring-Verbindungen, XXX Synthese und Eigenschaften von 4-Methoxy-1,5-benzothiazepin, einem einfachen Vertreter des 1,4-Thiazepin-Ringsystems/ Heterocyclic Seven-Membered Ring Compounds, XXX Synthesis and Properties of 4-Methoxy-1,5-benzothiazepine, a Simple Derivative of the 1,4-Thiazepine Ring System." Zeitschrift für Naturforschung B 42, no. 2 (February 1, 1987): 217–20. http://dx.doi.org/10.1515/znb-1987-0216.
Повний текст джерелаWigfield, Donald C., and Sherry L. Perkins. "Oxidation of elemental mercury by hydroperoxides in aqueous solution." Canadian Journal of Chemistry 63, no. 2 (February 1, 1985): 275–77. http://dx.doi.org/10.1139/v85-045.
Повний текст джерелаFossey, Jacques, Daniel Lefort, Massoud Massoudi, Jean-Yves Nedelec, and Jeanine Sorba. "Régiosélectivité et stéréosélectivité de l'hydroxylation homolytique des hydrocarbures par le peracide benzoïque." Canadian Journal of Chemistry 63, no. 3 (March 1, 1985): 678–80. http://dx.doi.org/10.1139/v85-111.
Повний текст джерелаCasida, J. E., and L. O. Ruzo. "Reactive intermediates in pesticide metabolism: Peracid oxidations as possible biomimetic models." Xenobiotica 16, no. 10-11 (January 1986): 1003–15. http://dx.doi.org/10.3109/00498258609038979.
Повний текст джерелаJumain Jalil, Mohd, Aliff Farhan Mohd Yamin, Mohd Saufi Md Zaini, Mohd Azahar Mohd Ariff, Siu Hua Chang, Norhashimah Morad, and Abdul Hadi. "Synthesis Of Epoxidized Oleic Acid- Based Palm Oil by Peracid Mechanism." IOP Conference Series: Materials Science and Engineering 551 (August 14, 2019): 012120. http://dx.doi.org/10.1088/1757-899x/551/1/012120.
Повний текст джерелаDavidson, R. Stephen, and Martin D. Walker. "Peracid and Acyl Peroxy Radical Mediated Oxidation and Rearrangement of Phosphoramides." Phosphorous and Sulfur and the Related Elements 30, no. 1-2 (March 1987): 305–10. http://dx.doi.org/10.1080/03086648708080582.
Повний текст джерелаChagonda, Lameck S., and Brian A. Marples. "Peracid oxidation of 16-arylidene- and 16-alkylidene-17-oxo-steroids." Journal of the Chemical Society, Perkin Transactions 1, no. 4 (1988): 875. http://dx.doi.org/10.1039/p19880000875.
Повний текст джерелаPeris, Gorka, and Scott J. Miller. "A Nonenzymatic Acid/Peracid Catalytic Cycle for the Baeyer−Villiger Oxidation." Organic Letters 10, no. 14 (July 2008): 3049–52. http://dx.doi.org/10.1021/ol8010248.
Повний текст джерелаWashington, Ilyas, and K. N. Houk. "Epoxidations by Peracid Anions in Water: Ambiphilic Oxenoid Reactivity and Stereoselectivity." Organic Letters 4, no. 16 (August 2002): 2661–64. http://dx.doi.org/10.1021/ol026105j.
Повний текст джерелаBenassi, Rois, Luca G. Fiandri, and Ferdinando Taddei. "Ab-Initio MO Study of the Peracid Oxidation of Dimethyl Thiosulfinate." Journal of Organic Chemistry 62, no. 23 (November 1997): 8018–23. http://dx.doi.org/10.1021/jo970758+.
Повний текст джерелаChakravarty, Ajit Kumar, Binayak Das, and Sibabrata Mukhopadhyay. "Peracid oxidation products of swertanone, the novel triterpene of Swertia chirata." Tetrahedron 47, no. 12-13 (1991): 2337–50. http://dx.doi.org/10.1016/s0040-4020(01)96141-1.
Повний текст джерелаBielawski, Jacek, and John E. Casida. "Phosphorylating intermediates in the peracid oxidation of phosphorothionates, phosphorothiolates, and phosphorodithioates." Journal of Agricultural and Food Chemistry 36, no. 3 (May 1988): 610–15. http://dx.doi.org/10.1021/jf00081a052.
Повний текст джерелаAndrus, Merritt B., and Benjamin W. Poehlein. "Epoxidation of olefins with peracid at low temperature with copper catalysis." Tetrahedron Letters 41, no. 7 (February 2000): 1013–14. http://dx.doi.org/10.1016/s0040-4039(00)00070-8.
Повний текст джерелаJacobsen, J. Steven, and M. Zafri Humayun. "Chloroperbenzoic acid induced DNA damage and peracid activation of alfatoxin B1." Carcinogenesis 7, no. 3 (1986): 491–93. http://dx.doi.org/10.1093/carcin/7.3.491.
Повний текст джерелаMalona, John A., Kevin Cariou, and Alison J. Frontier. "Nazarov Cyclization Initiated by Peracid Oxidation: The Total Synthesis of (±)-Rocaglamide." Journal of the American Chemical Society 131, no. 22 (June 10, 2009): 7560–61. http://dx.doi.org/10.1021/ja9029736.
Повний текст джерелаAzmi, Intan Suhada, Fakhrul Ariffin Md Nor Iskandar, Mohd Zulkipli Ab Kadir, and Mohd Jumain Jalil. "Sustainable Synthesis of Polyols Derived via In Situ Epoxidation Peracid Mechanism." Journal of The Institution of Engineers (India): Series E 104, no. 2 (December 2023): 269–74. http://dx.doi.org/10.1007/s40034-023-00279-3.
Повний текст джерелаHoang, Le-Thuy-Thuy-Trang, Thanh-Nha Tran, Thi-Phi-Giao Vo, Hoang-Vinh-Truong Phan, Phan-Si-Nguyen Dong, Dinh-Tri Mai, Ngoc-An Nguyen, et al. "Tinctoride A, a New Hopan-Type Triterpenoic Peracid from the Thallus of Lichen Parmotrema Tinctorum (Despr. ex Nyl.) Hale." Journal of Chemistry 2022 (April 11, 2022): 1–4. http://dx.doi.org/10.1155/2022/9092098.
Повний текст джерелаSchenk, Wolfdieter A., Johanna Leißner, and Christian Burschka. "Vier- und fünffach koordinierte Schwefelmonoxid-Komplexe des Rhodiums und Iridiums [1] / Four- and Five-Coordinated Sulfur Monoxide Complexes of Rhodium and Iridium [1 ]." Zeitschrift für Naturforschung B 40, no. 10 (October 1, 1985): 1264–73. http://dx.doi.org/10.1515/znb-1985-1007.
Повний текст джерела