Articoli di riviste sul 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. 30 (26 luglio 2004): 4061–64. http://dx.doi.org/10.1002/ange.200453872.
Abderrazak, 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. 39 (18 giugno 2021): 21268–84. http://dx.doi.org/10.1002/ange.202100270.
Herberg, 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. 1 (gennaio 1993): 117–27. http://dx.doi.org/10.1002/cber.19931260119.
Embo-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. 6 (21 marzo 2024): 1397. http://dx.doi.org/10.3390/molecules29061397.
Andrianasolo, 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. 4 (1 gennaio 2007): 593–602. http://dx.doi.org/10.1351/pac200779040593.
Nguyen, 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. 1 (30 dicembre 2022): 200. http://dx.doi.org/10.3390/polym15010200.
Albalat, 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. 19 (2020): 2916–24. http://dx.doi.org/10.1039/d0qo00559b.
Edeleva, 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. 5 (26 febbraio 2019): 688. http://dx.doi.org/10.3390/ma12050688.
Peuker, A., W. Hitzl, T. Jäger, B. Maier e A. Staudach. "Homologe intrauterine Insemination". Gynäkologische Endokrinologie 5, n. 2 (maggio 2007): 97–101. http://dx.doi.org/10.1007/s10304-007-0184-y.
Decher, H. "Radikalhöhlenverkleinerung durch homologe Knorpelchips*". Laryngo-Rhino-Otologie 64, n. 08 (agosto 1985): 423–26. http://dx.doi.org/10.1055/s-2007-1008172.
Koppenol, Willem H., e Reinhard Kissner. "Can ONOOH Undergo Homolysis?" Chemical Research in Toxicology 11, n. 2 (febbraio 1998): 87–90. http://dx.doi.org/10.1021/tx970200x.
Turrà, Natascia, Ulrich Neuenschwander e Ive Hermans. "Molecule-Induced Peroxide Homolysis". ChemPhysChem 14, n. 8 (4 aprile 2013): 1666–69. http://dx.doi.org/10.1002/cphc.201300130.
Guselnikova, 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. 11 (2021): 4154–61. http://dx.doi.org/10.1039/d0sc06470j.
Edeleva, 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. 2 (2019): 190–93. http://dx.doi.org/10.1039/c8cc08541b.
Chang, 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. 5 (2019): 1360–67. http://dx.doi.org/10.1039/c8sc03719a.
HUHTA, 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. 1 (26 febbraio 2001): 131–37. http://dx.doi.org/10.1042/bj3550131.
Sunada, 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. 1 (2016): 191–98. http://dx.doi.org/10.1039/c5sc02601f.
Antić, Aleksandar, e Nemanja Tomić. "Geoheritage and geotourism potential of the Homolje area (eastern Serbia)". Acta Geoturistica 8, n. 2 (20 dicembre 2017): 67–78. http://dx.doi.org/10.1515/agta-2017-0007.
Zhang, Sheng Jian, e Ying Xian Zhao. "Kinetics and Selectivity of Cyclohexane Pyrolysis". Advanced Materials Research 455-456 (gennaio 2012): 540–48. http://dx.doi.org/10.4028/www.scientific.net/amr.455-456.540.
Cherkasov, 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. 21 (1 novembre 2020): 5080. http://dx.doi.org/10.3390/molecules25215080.
Zhang, 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. 8 (2016): 6350–57. http://dx.doi.org/10.1039/c5ra22275c.
Zhao, 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. 123 (2015): 101412–15. http://dx.doi.org/10.1039/c5ra19244g.
Cameron, 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. 10 (1 ottobre 1995): 1627–38. http://dx.doi.org/10.1139/v95-202.
Audran, 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. 39 (2017): 8425–39. http://dx.doi.org/10.1039/c7ob02223a.
Li, 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.
Zhang, 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. 5 (2018): 793–96. http://dx.doi.org/10.1039/c7qo00926g.
Zheng, 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. 7 (2016): 2897–905. http://dx.doi.org/10.1039/c5dt03694a.
Riemer, R., K. F. Bürrig, K. P. Schulitz e H. Clahsen. "Der homologe Kreuzbandersatz im Tierexperiment". Sportverletzung · Sportschaden 2, n. 02 (giugno 1988): 72–79. http://dx.doi.org/10.1055/s-2007-993670.
Mezger, Fritz, Gerhard Simchen e Peter Fischer. "Die homologe "Silyl-Stobbe-Reaktion"". Synthesis 1991, n. 05 (1991): 375–78. http://dx.doi.org/10.1055/s-1991-26469.
Steffan, Carl R., James H. Espenson e Andreja Bakac. "Oxidative homolysis of organochromium macrocycles". Inorganic Chemistry 30, n. 5 (marzo 1991): 1134–37. http://dx.doi.org/10.1021/ic00005a046.
Bronz, L., C. Y. Genton, J. Kunz e W. E. Schreiner. "Reine homologe Uterussarkome 1960–1983". Archives of Gynecology 238, n. 1-4 (settembre 1985): 671–72. http://dx.doi.org/10.1007/bf02430163.
Prietl, G., G. Haidl e D. Krebs. "Sterilitätsbehandlung durch homologe intrauterine Insemination". Reproduktionsmedizin 16, n. 6 (14 dicembre 2000): 376–83. http://dx.doi.org/10.1007/s004440000226.
Li, 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. 12 (2014): 1690–98. http://dx.doi.org/10.1039/c4pp00321g.
Gong, 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. 50 (2015): 40269–82. http://dx.doi.org/10.1039/c5ra03828f.
Audran, 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. 93 (2015): 76660–65. http://dx.doi.org/10.1039/c5ra13899j.
Koirala, 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. 63 (2014): 33144–48. http://dx.doi.org/10.1039/c4ra05744a.
Nkolo, 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. 29 (2017): 6167–76. http://dx.doi.org/10.1039/c7ob01312d.
Nesterova, 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. 1 (2022): 282–99. http://dx.doi.org/10.1039/d1cy01991k.
Shin, Jeongcheol, Jiseon Lee, Jong-Min Suh e Kiyoung Park. "Ligand-field transition-induced C–S bond formation from nickelacycles". Chemical Science 12, n. 48 (2021): 15908–15. http://dx.doi.org/10.1039/d1sc05113j.
Audran, 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. 21 (2019): 3663–72. http://dx.doi.org/10.1039/c9qo00899c.
Audran, 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. 44 (2019): 25776–89. http://dx.doi.org/10.1039/c9ra05334d.
Torti, 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. 42 (2015): 33239–48. http://dx.doi.org/10.1039/c5ra03522h.
Audran, 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. 11 (2016): 1464–72. http://dx.doi.org/10.1039/c6qi00277c.
Schmale, Ine. "Ovarialkarzinom". Onkologische Welt 13, n. 05 (dicembre 2022): 292. http://dx.doi.org/10.1055/a-1939-6339.
Goertzen, M., A. Dellmann, J. Gruber, H. Clahsen e K. Bürrig. "Die homologe Kreuzbandtransplantation als intraartikulärer Bandersatz". Zeitschrift für Orthopädie und ihre Grenzgebiete 131, n. 02 (18 marzo 2008): 179–86. http://dx.doi.org/10.1055/s-2008-1040226.
Fokin, 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. 45 (novembre 2001): 11248–52. http://dx.doi.org/10.1021/ja0158096.
Sturzbecher-Höhne, Manuel, Thomas Nauser, Reinhard Kissner e Willem H. Koppenol. "Photon-Initiated Homolysis of Peroxynitrous Acid". Inorganic Chemistry 48, n. 15 (3 agosto 2009): 7307–12. http://dx.doi.org/10.1021/ic900614e.
Kreher, Richard P., Heidi Zimmermann e Christoph Sellinghoff. "Homologe Alkansäuren: Schmelzpunktalternanz Regelmäßigkeit oder Zufälligkeit?" CHEMKON 7, n. 4 (2000): 174–79. http://dx.doi.org/10.1002/ckon.20000070403.
Gaudel-Siri, Anouk, Didier Siri e Paul Tordo. "Homolysis ofN-alkoxyamines: A Computational Study". ChemPhysChem 7, n. 2 (6 febbraio 2006): 430–38. http://dx.doi.org/10.1002/cphc.200500308.
Song, Wenjing, e Andreja Bakac. "Oxidative Homolysis of a Nitrosylchromium Complex". Chemistry - A European Journal 14, n. 16 (29 maggio 2008): 4906–12. http://dx.doi.org/10.1002/chem.200701750.