Artigos de revistas sobre o tema "Homolyse"
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Wismach, Cathleen, Wolf-Walther du Mont, Peter G. Jones, Ludger Ernst, Ulrich Papke, Govindasamy Mugesh, Wolfgang Kaim, Matthias Wanner e Klaus D. Becker. "Selenol-Nitrosierung undSe-Nitrososelenol-Homolyse: ein Reaktionspfad mit möglichen biochemischen Implikationen". Angewandte Chemie 116, n.º 30 (26 de julho de 2004): 4061–64. http://dx.doi.org/10.1002/ange.200453872.
Texto completo da fonteAbderrazak, Youssef, Aditya Bhattacharyya e Oliver Reiser. "Durch sichtbares Licht induzierte Homolyse unedler, gut verfügbarer Metallsubstratkomplexe: Eine komplementäre Aktivierungsstrategie in der Photoredoxkatalyse". Angewandte Chemie 133, n.º 39 (18 de junho de 2021): 21268–84. http://dx.doi.org/10.1002/ange.202100270.
Texto completo da fonteHerberg, Clemens, Hans-;Dieter Beckhaus, Tamas Kürtvelyesi e 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, n.º 1 (janeiro de 1993): 117–27. http://dx.doi.org/10.1002/cber.19931260119.
Texto completo da fonteEmbo-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, n.º 6 (21 de março de 2024): 1397. http://dx.doi.org/10.3390/molecules29061397.
Texto completo da fonteAndrianasolo, Eric H., Douglas Goeger e William H. Gerwick. "Mitsoamide: A cytotoxic linear lipopeptide from the Madagascar marine cyanobacterium Geitlerinema sp." Pure and Applied Chemistry 79, n.º 4 (1 de janeiro de 2007): 593–602. http://dx.doi.org/10.1351/pac200779040593.
Texto completo da fonteNguyen, Thu Anh, Hui Ming Lim, Kenji Kinashi, Wataru Sakai, Naoto Tsutsumi, Satoko Okubayashi, Satoru Hosoda e Tetsu Sato. "Spin Trapping Analysis of Radical Intermediates on the Thermo-Oxidative Degradation of Polypropylene". Polymers 15, n.º 1 (30 de dezembro de 2022): 200. http://dx.doi.org/10.3390/polym15010200.
Texto completo da fonteAlbalat, Muriel, Gérard Audran, Maxence Holzritter, Sylvain R. A. Marque, Philippe Mellet, Nicolas Vanthuyne e Pierre Voisin. "An enzymatic acetal/hemiacetal conversion for the physiological temperature activation of the alkoxyamine C–ON bond homolysis". Organic Chemistry Frontiers 7, n.º 19 (2020): 2916–24. http://dx.doi.org/10.1039/d0qo00559b.
Texto completo da fonteEdeleva, Mariya, Gerard Audran, Sylvain Marque e Elena Bagryanskaya. "Smart Control of Nitroxide-Mediated Polymerization Initiators’ Reactivity by pH, Complexation with Metals, and Chemical Transformations". Materials 12, n.º 5 (26 de fevereiro de 2019): 688. http://dx.doi.org/10.3390/ma12050688.
Texto completo da fontePeuker, A., W. Hitzl, T. Jäger, B. Maier e A. Staudach. "Homologe intrauterine Insemination". Gynäkologische Endokrinologie 5, n.º 2 (maio de 2007): 97–101. http://dx.doi.org/10.1007/s10304-007-0184-y.
Texto completo da fonteDecher, H. "Radikalhöhlenverkleinerung durch homologe Knorpelchips*". Laryngo-Rhino-Otologie 64, n.º 08 (agosto de 1985): 423–26. http://dx.doi.org/10.1055/s-2007-1008172.
Texto completo da fonteKoppenol, Willem H., e Reinhard Kissner. "Can ONOOH Undergo Homolysis?" Chemical Research in Toxicology 11, n.º 2 (fevereiro de 1998): 87–90. http://dx.doi.org/10.1021/tx970200x.
Texto completo da fonteTurrà, Natascia, Ulrich Neuenschwander e Ive Hermans. "Molecule-Induced Peroxide Homolysis". ChemPhysChem 14, n.º 8 (4 de abril de 2013): 1666–69. http://dx.doi.org/10.1002/cphc.201300130.
Texto completo da fonteGuselnikova, Olga, Gérard Audran, Jean-Patrick Joly, Andrii Trelin, Evgeny V. Tretyakov, Vaclav Svorcik, Oleksiy Lyutakov, Sylvain R. A. Marque e Pavel Postnikov. "Establishing plasmon contribution to chemical reactions: alkoxyamines as a thermal probe". Chemical Science 12, n.º 11 (2021): 4154–61. http://dx.doi.org/10.1039/d0sc06470j.
Texto completo da fonteEdeleva, Mariya, Denis Morozov, Dmitriy Parkhomenko, Yulia Polienko, Anna Iurchenkova, Igor Kirilyuk e Elena Bagryanskaya. "Versatile approach to activation of alkoxyamine homolysis by 1,3-dipolar cycloaddition for efficient and safe nitroxide mediated polymerization". Chemical Communications 55, n.º 2 (2019): 190–93. http://dx.doi.org/10.1039/c8cc08541b.
Texto completo da fonteChang, Mu-Chieh, Kate A. Jesse, Alexander S. Filatov e John S. Anderson. "Reversible homolytic activation of water via metal–ligand cooperativity in a T-shaped Ni(ii) complex". Chemical Science 10, n.º 5 (2019): 1360–67. http://dx.doi.org/10.1039/c8sc03719a.
Texto completo da fonteHUHTA, Marja S., Hao-Ping CHEN, Craig HEMANN, C. Russ HILLE e E. Neil G. MARSH. "Protein–coenzyme interactions in adenosylcobalamin-dependent glutamate mutase". Biochemical Journal 355, n.º 1 (26 de fevereiro de 2001): 131–37. http://dx.doi.org/10.1042/bj3550131.
Texto completo da fonteSunada, Yusuke, Shintaro Ishida, Fumiya Hirakawa, Yoshihito Shiota, Kazunari Yoshizawa, Shinji Kanegawa, Osamu Sato, Hideo Nagashima e Takeaki Iwamoto. "Persistent four-coordinate iron-centered radical stabilized by π-donation". Chemical Science 7, n.º 1 (2016): 191–98. http://dx.doi.org/10.1039/c5sc02601f.
Texto completo da fonteAntić, Aleksandar, e Nemanja Tomić. "Geoheritage and geotourism potential of the Homolje area (eastern Serbia)". Acta Geoturistica 8, n.º 2 (20 de dezembro de 2017): 67–78. http://dx.doi.org/10.1515/agta-2017-0007.
Texto completo da fonteZhang, Sheng Jian, e Ying Xian Zhao. "Kinetics and Selectivity of Cyclohexane Pyrolysis". Advanced Materials Research 455-456 (janeiro de 2012): 540–48. http://dx.doi.org/10.4028/www.scientific.net/amr.455-456.540.
Texto completo da fonteCherkasov, Sergey, Dmitriy Parkhomenko, Alexander Genaev, Georgii Salnikov, Mariya Edeleva, Denis Morozov, Tatyana Rybalova, Igor Kirilyuk, Sylvain R. A. Marque e Elena Bagryanskaya. "NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines". Molecules 25, n.º 21 (1 de novembro de 2020): 5080. http://dx.doi.org/10.3390/molecules25215080.
Texto completo da fonteZhang, Ze Ping, Yan Lu, Min Zhi Rong e Ming Qiu Zhang. "A thermally remendable and reprocessable crosslinked methyl methacrylate polymer based on oxygen insensitive dynamic reversible C–ON bonds". RSC Advances 6, n.º 8 (2016): 6350–57. http://dx.doi.org/10.1039/c5ra22275c.
Texto completo da fonteZhao, Bo, Ju-You Lu, Yang Li, Dong-Huai Tu, Zhao-Tie Liu, Zhong-Wen Liu e Jian Lu. "Regioisomerized atom transfer radical addition (ATRA) of olefins with dichlorofluorocarbons". RSC Advances 5, n.º 123 (2015): 101412–15. http://dx.doi.org/10.1039/c5ra19244g.
Texto completo da fonteCameron, Dale R., Alison M. P. Borrajo, Gregory R. J. Thatcher e 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, n.º 10 (1 de outubro de 1995): 1627–38. http://dx.doi.org/10.1139/v95-202.
Texto completo da fonteAudran, Gérard, Raphael Bikanga, Paul Brémond, Mariya Edeleva, Jean-Patrick Joly, Sylvain R. A. Marque, Paulin Nkolo e Valérie Roubaud. "How intramolecular hydrogen bonding (IHB) controls the C–ON bond homolysis in alkoxyamines". Organic & Biomolecular Chemistry 15, n.º 39 (2017): 8425–39. http://dx.doi.org/10.1039/c7ob02223a.
Texto completo da fonteLi, Hong Zhi, Lin Li, Zi Yan Zhong, Yi Han, LiHong Hu e 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.
Texto completo da fonteZhang, Chen, Junxia Pi, Shu Chen, Ping Liu e 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, n.º 5 (2018): 793–96. http://dx.doi.org/10.1039/c7qo00926g.
Texto completo da fonteZheng, Yue, Qian-Xiong Zhou, Yang-Yang Zhang, Chao Li, Yuan-Jun Hou e 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, n.º 7 (2016): 2897–905. http://dx.doi.org/10.1039/c5dt03694a.
Texto completo da fonteRiemer, R., K. F. Bürrig, K. P. Schulitz e H. Clahsen. "Der homologe Kreuzbandersatz im Tierexperiment". Sportverletzung · Sportschaden 2, n.º 02 (junho de 1988): 72–79. http://dx.doi.org/10.1055/s-2007-993670.
Texto completo da fonteMezger, Fritz, Gerhard Simchen e Peter Fischer. "Die homologe "Silyl-Stobbe-Reaktion"". Synthesis 1991, n.º 05 (1991): 375–78. http://dx.doi.org/10.1055/s-1991-26469.
Texto completo da fonteSteffan, Carl R., James H. Espenson e Andreja Bakac. "Oxidative homolysis of organochromium macrocycles". Inorganic Chemistry 30, n.º 5 (março de 1991): 1134–37. http://dx.doi.org/10.1021/ic00005a046.
Texto completo da fonteBronz, L., C. Y. Genton, J. Kunz e W. E. Schreiner. "Reine homologe Uterussarkome 1960–1983". Archives of Gynecology 238, n.º 1-4 (setembro de 1985): 671–72. http://dx.doi.org/10.1007/bf02430163.
Texto completo da fontePrietl, G., G. Haidl e D. Krebs. "Sterilitätsbehandlung durch homologe intrauterine Insemination". Reproduktionsmedizin 16, n.º 6 (14 de dezembro de 2000): 376–83. http://dx.doi.org/10.1007/s004440000226.
Texto completo da fonteLi, Jun, Yang Yang, Ping Zhang, James R. Sounik e Malcolm E. Kenney. "Synthesis, properties and drug potential of the photosensitive alkyl- and alkylsiloxy-ligated silicon phthalocyanine Pc 227". Photochem. Photobiol. Sci. 13, n.º 12 (2014): 1690–98. http://dx.doi.org/10.1039/c4pp00321g.
Texto completo da fonteGong, Xianyun, Hongjun Kang, Yuyan Liu e Songquan Wu. "Decomposition mechanisms and kinetics of amine/anhydride-cured DGEBA epoxy resin in near-critical water". RSC Advances 5, n.º 50 (2015): 40269–82. http://dx.doi.org/10.1039/c5ra03828f.
Texto completo da fonteAudran, Gerard, Matisse Batsiandzy Ibanou, Paul Brémond, Jean-Patrick Joly e Sylvain R. A. Marque. "Part 10: chemically triggered alkoxyamine C–ON bond homolysis in ionic liquid solvents". RSC Advances 5, n.º 93 (2015): 76660–65. http://dx.doi.org/10.1039/c5ra13899j.
Texto completo da fonteKoirala, Agni Raj, Son Docao e Kyung Byung Yoon. "Photocatalytic homolysis of methyl formate to dry formaldehyde on PdO/TiO2: photocatalytic reverse Tishchenko reaction of methyl formate". RSC Adv. 4, n.º 63 (2014): 33144–48. http://dx.doi.org/10.1039/c4ra05744a.
Texto completo da fonteNkolo, Paulin, Gérard Audran, Raphael Bikanga, Paul Brémond, Sylvain R. A. Marque e Valérie Roubaud. "C–ON bond homolysis of alkoxyamines: when too high polarity is detrimental". Organic & Biomolecular Chemistry 15, n.º 29 (2017): 6167–76. http://dx.doi.org/10.1039/c7ob01312d.
Texto completo da fonteNesterova, Oksana V., Maxim L. Kuznetsov, Armando J. L. Pombeiro, Georgiy B. Shul'pin e 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, n.º 1 (2022): 282–99. http://dx.doi.org/10.1039/d1cy01991k.
Texto completo da fonteShin, Jeongcheol, Jiseon Lee, Jong-Min Suh e Kiyoung Park. "Ligand-field transition-induced C–S bond formation from nickelacycles". Chemical Science 12, n.º 48 (2021): 15908–15. http://dx.doi.org/10.1039/d1sc05113j.
Texto completo da fonteAudran, 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, n.º 21 (2019): 3663–72. http://dx.doi.org/10.1039/c9qo00899c.
Texto completo da fonteAudran, 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, n.º 44 (2019): 25776–89. http://dx.doi.org/10.1039/c9ra05334d.
Texto completo da fonteTorti, Edoardo, Gioia Della Giustina, Stefano Protti, Daniele Merli, Giovanna Brusatin e Maurizio Fagnoni. "Aryl tosylates as non-ionic photoacid generators (PAGs): photochemistry and applications in cationic photopolymerizations". RSC Advances 5, n.º 42 (2015): 33239–48. http://dx.doi.org/10.1039/c5ra03522h.
Texto completo da fonteAudran, Gérard, Elena Bagryanskaya, Irina Bagryanskaya, Paul Brémond, Mariya Edeleva, Sylvain R. A. Marque, Dmitriy Parkhomenko, Evgeny Tretyakov e Svetlana Zhivetyeva. "C–ON bond homolysis of alkoxyamines triggered by paramagnetic copper(ii) salts". Inorganic Chemistry Frontiers 3, n.º 11 (2016): 1464–72. http://dx.doi.org/10.1039/c6qi00277c.
Texto completo da fonteSchmale, Ine. "Ovarialkarzinom". Onkologische Welt 13, n.º 05 (dezembro de 2022): 292. http://dx.doi.org/10.1055/a-1939-6339.
Texto completo da fonteGoertzen, M., A. Dellmann, J. Gruber, H. Clahsen e K. Bürrig. "Die homologe Kreuzbandtransplantation als intraartikulärer Bandersatz". Zeitschrift für Orthopädie und ihre Grenzgebiete 131, n.º 02 (18 de março de 2008): 179–86. http://dx.doi.org/10.1055/s-2008-1040226.
Texto completo da fonteFokin, Andrey A., Boryslav A. Tkachenko, Oleg I. Korshunov, Pavel A. Gunchenko e Peter R. Schreiner. "Molecule-Induced Alkane Homolysis with Dioxiranes". Journal of the American Chemical Society 123, n.º 45 (novembro de 2001): 11248–52. http://dx.doi.org/10.1021/ja0158096.
Texto completo da fonteSturzbecher-Höhne, Manuel, Thomas Nauser, Reinhard Kissner e Willem H. Koppenol. "Photon-Initiated Homolysis of Peroxynitrous Acid". Inorganic Chemistry 48, n.º 15 (3 de agosto de 2009): 7307–12. http://dx.doi.org/10.1021/ic900614e.
Texto completo da fonteKreher, Richard P., Heidi Zimmermann e Christoph Sellinghoff. "Homologe Alkansäuren: Schmelzpunktalternanz Regelmäßigkeit oder Zufälligkeit?" CHEMKON 7, n.º 4 (2000): 174–79. http://dx.doi.org/10.1002/ckon.20000070403.
Texto completo da fonteGaudel-Siri, Anouk, Didier Siri e Paul Tordo. "Homolysis ofN-alkoxyamines: A Computational Study". ChemPhysChem 7, n.º 2 (6 de fevereiro de 2006): 430–38. http://dx.doi.org/10.1002/cphc.200500308.
Texto completo da fonteSong, Wenjing, e Andreja Bakac. "Oxidative Homolysis of a Nitrosylchromium Complex". Chemistry - A European Journal 14, n.º 16 (29 de maio de 2008): 4906–12. http://dx.doi.org/10.1002/chem.200701750.
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