Статті в журналах з теми "Homolyse"
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Wismach, Cathleen, Wolf-Walther du Mont, Peter G. Jones, Ludger Ernst, Ulrich Papke, Govindasamy Mugesh, Wolfgang Kaim, Matthias Wanner, and Klaus D. Becker. "Selenol-Nitrosierung undSe-Nitrososelenol-Homolyse: ein Reaktionspfad mit möglichen biochemischen Implikationen." Angewandte Chemie 116, no. 30 (July 26, 2004): 4061–64. http://dx.doi.org/10.1002/ange.200453872.
Повний текст джерелаAbderrazak, Youssef, Aditya Bhattacharyya, and Oliver Reiser. "Durch sichtbares Licht induzierte Homolyse unedler, gut verfügbarer Metallsubstratkomplexe: Eine komplementäre Aktivierungsstrategie in der Photoredoxkatalyse." Angewandte Chemie 133, no. 39 (June 18, 2021): 21268–84. http://dx.doi.org/10.1002/ange.202100270.
Повний текст джерелаHerberg, Clemens, Hans-;Dieter Beckhaus, Tamas Kürtvelyesi, and Christoph Rüchardt. "Thermolabile Kohlenwasserstoffe, 32. Konkurrierende Cope-;Umlagerung und Homolyse vonmeso- undDL-3,4-Di(1-cyclohexen-1-yl)-2,2,5,5-tetramethylhexan." Chemische Berichte 126, no. 1 (January 1993): 117–27. http://dx.doi.org/10.1002/cber.19931260119.
Повний текст джерелаEmbo-Ibouanga, Ange W., Michel Nguyen, Lucie Paloque, Mathilde Coustets, Jean-Patrick Joly, Jean-Michel Augereau, Nicolas Vanthuyne, et al. "Hybrid Peptide-Alkoxyamine Drugs: A Strategy for the Development of a New Family of Antiplasmodial Drugs." Molecules 29, no. 6 (March 21, 2024): 1397. http://dx.doi.org/10.3390/molecules29061397.
Повний текст джерелаAndrianasolo, Eric H., Douglas Goeger, and William H. Gerwick. "Mitsoamide: A cytotoxic linear lipopeptide from the Madagascar marine cyanobacterium Geitlerinema sp." Pure and Applied Chemistry 79, no. 4 (January 1, 2007): 593–602. http://dx.doi.org/10.1351/pac200779040593.
Повний текст джерелаNguyen, Thu Anh, Hui Ming Lim, Kenji Kinashi, Wataru Sakai, Naoto Tsutsumi, Satoko Okubayashi, Satoru Hosoda, and Tetsu Sato. "Spin Trapping Analysis of Radical Intermediates on the Thermo-Oxidative Degradation of Polypropylene." Polymers 15, no. 1 (December 30, 2022): 200. http://dx.doi.org/10.3390/polym15010200.
Повний текст джерелаAlbalat, Muriel, Gérard Audran, Maxence Holzritter, Sylvain R. A. Marque, Philippe Mellet, Nicolas Vanthuyne, and Pierre Voisin. "An enzymatic acetal/hemiacetal conversion for the physiological temperature activation of the alkoxyamine C–ON bond homolysis." Organic Chemistry Frontiers 7, no. 19 (2020): 2916–24. http://dx.doi.org/10.1039/d0qo00559b.
Повний текст джерелаEdeleva, Mariya, Gerard Audran, Sylvain Marque, and Elena Bagryanskaya. "Smart Control of Nitroxide-Mediated Polymerization Initiators’ Reactivity by pH, Complexation with Metals, and Chemical Transformations." Materials 12, no. 5 (February 26, 2019): 688. http://dx.doi.org/10.3390/ma12050688.
Повний текст джерелаPeuker, A., W. Hitzl, T. Jäger, B. Maier, and A. Staudach. "Homologe intrauterine Insemination." Gynäkologische Endokrinologie 5, no. 2 (May 2007): 97–101. http://dx.doi.org/10.1007/s10304-007-0184-y.
Повний текст джерелаDecher, H. "Radikalhöhlenverkleinerung durch homologe Knorpelchips*." Laryngo-Rhino-Otologie 64, no. 08 (August 1985): 423–26. http://dx.doi.org/10.1055/s-2007-1008172.
Повний текст джерелаKoppenol, Willem H., and Reinhard Kissner. "Can ONOOH Undergo Homolysis?" Chemical Research in Toxicology 11, no. 2 (February 1998): 87–90. http://dx.doi.org/10.1021/tx970200x.
Повний текст джерелаTurrà, Natascia, Ulrich Neuenschwander, and Ive Hermans. "Molecule-Induced Peroxide Homolysis." ChemPhysChem 14, no. 8 (April 4, 2013): 1666–69. http://dx.doi.org/10.1002/cphc.201300130.
Повний текст джерелаGuselnikova, Olga, Gérard Audran, Jean-Patrick Joly, Andrii Trelin, Evgeny V. Tretyakov, Vaclav Svorcik, Oleksiy Lyutakov, Sylvain R. A. Marque, and Pavel Postnikov. "Establishing plasmon contribution to chemical reactions: alkoxyamines as a thermal probe." Chemical Science 12, no. 11 (2021): 4154–61. http://dx.doi.org/10.1039/d0sc06470j.
Повний текст джерелаEdeleva, Mariya, Denis Morozov, Dmitriy Parkhomenko, Yulia Polienko, Anna Iurchenkova, Igor Kirilyuk, and Elena Bagryanskaya. "Versatile approach to activation of alkoxyamine homolysis by 1,3-dipolar cycloaddition for efficient and safe nitroxide mediated polymerization." Chemical Communications 55, no. 2 (2019): 190–93. http://dx.doi.org/10.1039/c8cc08541b.
Повний текст джерелаChang, Mu-Chieh, Kate A. Jesse, Alexander S. Filatov, and John S. Anderson. "Reversible homolytic activation of water via metal–ligand cooperativity in a T-shaped Ni(ii) complex." Chemical Science 10, no. 5 (2019): 1360–67. http://dx.doi.org/10.1039/c8sc03719a.
Повний текст джерелаHUHTA, Marja S., Hao-Ping CHEN, Craig HEMANN, C. Russ HILLE, and E. Neil G. MARSH. "Protein–coenzyme interactions in adenosylcobalamin-dependent glutamate mutase." Biochemical Journal 355, no. 1 (February 26, 2001): 131–37. http://dx.doi.org/10.1042/bj3550131.
Повний текст джерелаSunada, Yusuke, Shintaro Ishida, Fumiya Hirakawa, Yoshihito Shiota, Kazunari Yoshizawa, Shinji Kanegawa, Osamu Sato, Hideo Nagashima та Takeaki Iwamoto. "Persistent four-coordinate iron-centered radical stabilized by π-donation". Chemical Science 7, № 1 (2016): 191–98. http://dx.doi.org/10.1039/c5sc02601f.
Повний текст джерелаAntić, Aleksandar, and Nemanja Tomić. "Geoheritage and geotourism potential of the Homolje area (eastern Serbia)." Acta Geoturistica 8, no. 2 (December 20, 2017): 67–78. http://dx.doi.org/10.1515/agta-2017-0007.
Повний текст джерелаZhang, Sheng Jian, and Ying Xian Zhao. "Kinetics and Selectivity of Cyclohexane Pyrolysis." Advanced Materials Research 455-456 (January 2012): 540–48. http://dx.doi.org/10.4028/www.scientific.net/amr.455-456.540.
Повний текст джерелаCherkasov, Sergey, Dmitriy Parkhomenko, Alexander Genaev, Georgii Salnikov, Mariya Edeleva, Denis Morozov, Tatyana Rybalova, Igor Kirilyuk, Sylvain R. A. Marque, and Elena Bagryanskaya. "NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines." Molecules 25, no. 21 (November 1, 2020): 5080. http://dx.doi.org/10.3390/molecules25215080.
Повний текст джерелаZhang, Ze Ping, Yan Lu, Min Zhi Rong, and Ming Qiu Zhang. "A thermally remendable and reprocessable crosslinked methyl methacrylate polymer based on oxygen insensitive dynamic reversible C–ON bonds." RSC Advances 6, no. 8 (2016): 6350–57. http://dx.doi.org/10.1039/c5ra22275c.
Повний текст джерелаZhao, Bo, Ju-You Lu, Yang Li, Dong-Huai Tu, Zhao-Tie Liu, Zhong-Wen Liu, and Jian Lu. "Regioisomerized atom transfer radical addition (ATRA) of olefins with dichlorofluorocarbons." RSC Advances 5, no. 123 (2015): 101412–15. http://dx.doi.org/10.1039/c5ra19244g.
Повний текст джерелаCameron, Dale R., Alison M. P. Borrajo, Gregory R. J. Thatcher, and Brian M. Bennett. "Organic nitrates, thionitrates, peroxynitrites, and nitric oxide: a molecular orbital study of the (X = O, S) rearrangement, a reaction of potential biological significance." Canadian Journal of Chemistry 73, no. 10 (October 1, 1995): 1627–38. http://dx.doi.org/10.1139/v95-202.
Повний текст джерелаAudran, Gérard, Raphael Bikanga, Paul Brémond, Mariya Edeleva, Jean-Patrick Joly, Sylvain R. A. Marque, Paulin Nkolo, and Valérie Roubaud. "How intramolecular hydrogen bonding (IHB) controls the C–ON bond homolysis in alkoxyamines." Organic & Biomolecular Chemistry 15, no. 39 (2017): 8425–39. http://dx.doi.org/10.1039/c7ob02223a.
Повний текст джерелаLi, Hong Zhi, Lin Li, Zi Yan Zhong, Yi Han, LiHong Hu, and Ying Hua Lu. "An Accurate and Efficient Method to Predict Y-NO Bond Homolysis Bond Dissociation Energies." Mathematical Problems in Engineering 2013 (2013): 1–10. http://dx.doi.org/10.1155/2013/860357.
Повний текст джерелаZhang, Chen, Junxia Pi, Shu Chen, Ping Liu, and Peipei Sun. "Construction of a 4H-pyrido[4,3,2-gh]phenanthridin-5(6H)-one skeleton via a catalyst-free radical cascade addition/cyclization using azo compounds as radical sources." Organic Chemistry Frontiers 5, no. 5 (2018): 793–96. http://dx.doi.org/10.1039/c7qo00926g.
Повний текст джерелаZheng, Yue, Qian-Xiong Zhou, Yang-Yang Zhang, Chao Li, Yuan-Jun Hou, and Xue-Song Wang. "Substituent effect and wavelength dependence of the photoinduced Ru–O homolysis in the [Ru(bpy)2(py-SO3)]+-type complexes." Dalton Transactions 45, no. 7 (2016): 2897–905. http://dx.doi.org/10.1039/c5dt03694a.
Повний текст джерелаRiemer, R., K. F. Bürrig, K. P. Schulitz, and H. Clahsen. "Der homologe Kreuzbandersatz im Tierexperiment." Sportverletzung · Sportschaden 2, no. 02 (June 1988): 72–79. http://dx.doi.org/10.1055/s-2007-993670.
Повний текст джерелаMezger, Fritz, Gerhard Simchen, and Peter Fischer. "Die homologe "Silyl-Stobbe-Reaktion"." Synthesis 1991, no. 05 (1991): 375–78. http://dx.doi.org/10.1055/s-1991-26469.
Повний текст джерелаSteffan, Carl R., James H. Espenson, and Andreja Bakac. "Oxidative homolysis of organochromium macrocycles." Inorganic Chemistry 30, no. 5 (March 1991): 1134–37. http://dx.doi.org/10.1021/ic00005a046.
Повний текст джерелаBronz, L., C. Y. Genton, J. Kunz, and W. E. Schreiner. "Reine homologe Uterussarkome 1960–1983." Archives of Gynecology 238, no. 1-4 (September 1985): 671–72. http://dx.doi.org/10.1007/bf02430163.
Повний текст джерелаPrietl, G., G. Haidl, and D. Krebs. "Sterilitätsbehandlung durch homologe intrauterine Insemination." Reproduktionsmedizin 16, no. 6 (December 14, 2000): 376–83. http://dx.doi.org/10.1007/s004440000226.
Повний текст джерелаLi, Jun, Yang Yang, Ping Zhang, James R. Sounik, and Malcolm E. Kenney. "Synthesis, properties and drug potential of the photosensitive alkyl- and alkylsiloxy-ligated silicon phthalocyanine Pc 227." Photochem. Photobiol. Sci. 13, no. 12 (2014): 1690–98. http://dx.doi.org/10.1039/c4pp00321g.
Повний текст джерелаGong, Xianyun, Hongjun Kang, Yuyan Liu, and Songquan Wu. "Decomposition mechanisms and kinetics of amine/anhydride-cured DGEBA epoxy resin in near-critical water." RSC Advances 5, no. 50 (2015): 40269–82. http://dx.doi.org/10.1039/c5ra03828f.
Повний текст джерелаAudran, Gerard, Matisse Batsiandzy Ibanou, Paul Brémond, Jean-Patrick Joly, and Sylvain R. A. Marque. "Part 10: chemically triggered alkoxyamine C–ON bond homolysis in ionic liquid solvents." RSC Advances 5, no. 93 (2015): 76660–65. http://dx.doi.org/10.1039/c5ra13899j.
Повний текст джерелаKoirala, Agni Raj, Son Docao, and Kyung Byung Yoon. "Photocatalytic homolysis of methyl formate to dry formaldehyde on PdO/TiO2: photocatalytic reverse Tishchenko reaction of methyl formate." RSC Adv. 4, no. 63 (2014): 33144–48. http://dx.doi.org/10.1039/c4ra05744a.
Повний текст джерелаNkolo, Paulin, Gérard Audran, Raphael Bikanga, Paul Brémond, Sylvain R. A. Marque, and Valérie Roubaud. "C–ON bond homolysis of alkoxyamines: when too high polarity is detrimental." Organic & Biomolecular Chemistry 15, no. 29 (2017): 6167–76. http://dx.doi.org/10.1039/c7ob01312d.
Повний текст джерелаNesterova, Oksana V., Maxim L. Kuznetsov, Armando J. L. Pombeiro, Georgiy B. Shul'pin, and Dmytro S. Nesterov. "Homogeneous oxidation of C–H bonds with m-CPBA catalysed by a Co/Fe system: mechanistic insights from the point of view of the oxidant." Catalysis Science & Technology 12, no. 1 (2022): 282–99. http://dx.doi.org/10.1039/d1cy01991k.
Повний текст джерелаShin, Jeongcheol, Jiseon Lee, Jong-Min Suh, and Kiyoung Park. "Ligand-field transition-induced C–S bond formation from nickelacycles." Chemical Science 12, no. 48 (2021): 15908–15. http://dx.doi.org/10.1039/d1sc05113j.
Повний текст джерелаAudran, Gérard, Lionel Bosco, Paul Brémond, Natacha Jugniot, Sylvain R. A. Marque, Philippe Massot, Philippe Mellet, et al. "Enzymatic triggering of C–ON bond homolysis of alkoxyamines." Organic Chemistry Frontiers 6, no. 21 (2019): 3663–72. http://dx.doi.org/10.1039/c9qo00899c.
Повний текст джерелаAudran, Gérard, Elena Bagryanskaya, Irina Bagryanskaya, Mariya Edeleva, Jean-Patrick Joly, Sylvain R. A. Marque, Anna Iurchenkova, et al. "How intramolecular coordination bonding (ICB) controls the homolysis of the C–ON bond in alkoxyamines." RSC Advances 9, no. 44 (2019): 25776–89. http://dx.doi.org/10.1039/c9ra05334d.
Повний текст джерелаTorti, Edoardo, Gioia Della Giustina, Stefano Protti, Daniele Merli, Giovanna Brusatin, and Maurizio Fagnoni. "Aryl tosylates as non-ionic photoacid generators (PAGs): photochemistry and applications in cationic photopolymerizations." RSC Advances 5, no. 42 (2015): 33239–48. http://dx.doi.org/10.1039/c5ra03522h.
Повний текст джерелаAudran, Gérard, Elena Bagryanskaya, Irina Bagryanskaya, Paul Brémond, Mariya Edeleva, Sylvain R. A. Marque, Dmitriy Parkhomenko, Evgeny Tretyakov, and Svetlana Zhivetyeva. "C–ON bond homolysis of alkoxyamines triggered by paramagnetic copper(ii) salts." Inorganic Chemistry Frontiers 3, no. 11 (2016): 1464–72. http://dx.doi.org/10.1039/c6qi00277c.
Повний текст джерелаSchmale, Ine. "Ovarialkarzinom." Onkologische Welt 13, no. 05 (December 2022): 292. http://dx.doi.org/10.1055/a-1939-6339.
Повний текст джерелаGoertzen, M., A. Dellmann, J. Gruber, H. Clahsen, and K. Bürrig. "Die homologe Kreuzbandtransplantation als intraartikulärer Bandersatz." Zeitschrift für Orthopädie und ihre Grenzgebiete 131, no. 02 (March 18, 2008): 179–86. http://dx.doi.org/10.1055/s-2008-1040226.
Повний текст джерелаFokin, Andrey A., Boryslav A. Tkachenko, Oleg I. Korshunov, Pavel A. Gunchenko, and Peter R. Schreiner. "Molecule-Induced Alkane Homolysis with Dioxiranes." Journal of the American Chemical Society 123, no. 45 (November 2001): 11248–52. http://dx.doi.org/10.1021/ja0158096.
Повний текст джерелаSturzbecher-Höhne, Manuel, Thomas Nauser, Reinhard Kissner, and Willem H. Koppenol. "Photon-Initiated Homolysis of Peroxynitrous Acid." Inorganic Chemistry 48, no. 15 (August 3, 2009): 7307–12. http://dx.doi.org/10.1021/ic900614e.
Повний текст джерелаKreher, Richard P., Heidi Zimmermann, and Christoph Sellinghoff. "Homologe Alkansäuren: Schmelzpunktalternanz Regelmäßigkeit oder Zufälligkeit?" CHEMKON 7, no. 4 (2000): 174–79. http://dx.doi.org/10.1002/ckon.20000070403.
Повний текст джерелаGaudel-Siri, Anouk, Didier Siri, and Paul Tordo. "Homolysis ofN-alkoxyamines: A Computational Study." ChemPhysChem 7, no. 2 (February 6, 2006): 430–38. http://dx.doi.org/10.1002/cphc.200500308.
Повний текст джерелаSong, Wenjing, and Andreja Bakac. "Oxidative Homolysis of a Nitrosylchromium Complex." Chemistry - A European Journal 14, no. 16 (May 29, 2008): 4906–12. http://dx.doi.org/10.1002/chem.200701750.
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