Auswahl der wissenschaftlichen Literatur zum Thema „Photoredox catalytic system“
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Zeitschriftenartikel zum Thema "Photoredox catalytic system"
Yang, Qiong, Fengqian Zhao, Na Zhang, Mingke Liu, Huanhuan Hu, Jingjie Zhang und Shaolin Zhou. „Mild dynamic kinetic resolution of amines by coupled visible-light photoredox and enzyme catalysis“. Chemical Communications 54, Nr. 100 (2018): 14065–68. http://dx.doi.org/10.1039/c8cc07990k.
Der volle Inhalt der QuelleLeadbeater, Nicholas, Jyoti Nandi und Mason Witko. „Combining Oxoammonium Cation Mediated Oxidation and Photoredox Catalysis for the Conversion of Aldehydes into Nitriles“. Synlett 29, Nr. 16 (12.09.2018): 2185–90. http://dx.doi.org/10.1055/s-0037-1610272.
Der volle Inhalt der QuelleTlahuext-Aca, Adrian, Matthew N. Hopkinson, Basudev Sahoo und Frank Glorius. „Dual gold/photoredox-catalyzed C(sp)–H arylation of terminal alkynes with diazonium salts“. Chemical Science 7, Nr. 1 (2016): 89–93. http://dx.doi.org/10.1039/c5sc02583d.
Der volle Inhalt der QuelleHu, Xia, Guoting Zhang, Faxiang Bu, Xu Luo, Kebing Yi, Heng Zhang und Aiwen Lei. „Photoinduced oxidative activation of electron-rich arenes: alkenylation with H2 evolution under external oxidant-free conditions“. Chemical Science 9, Nr. 6 (2018): 1521–26. http://dx.doi.org/10.1039/c7sc04634k.
Der volle Inhalt der QuelleHossain, Asik, Aditya Bhattacharyya und Oliver Reiser. „Copper’s rapid ascent in visible-light photoredox catalysis“. Science 364, Nr. 6439 (02.05.2019): eaav9713. http://dx.doi.org/10.1126/science.aav9713.
Der volle Inhalt der QuelleNaumann, Robert, Christoph Kerzig und Martin Goez. „Laboratory-scale photoredox catalysis using hydrated electrons sustainably generated with a single green laser“. Chem. Sci. 8, Nr. 11 (2017): 7510–20. http://dx.doi.org/10.1039/c7sc03514d.
Der volle Inhalt der QuellePagire, Santosh K., Naoya Kumagai und Masakatsu Shibasaki. „Introduction of a 7-aza-6-MeO-indoline auxiliary in Lewis-acid/photoredox cooperative catalysis: highly enantioselective aminomethylation of α,β-unsaturated amides“. Chemical Science 11, Nr. 20 (2020): 5168–74. http://dx.doi.org/10.1039/d0sc01890b.
Der volle Inhalt der QuelleKostromitin, Vladislav S., Vitalij V. Levin und Alexander D. Dilman. „Atom Transfer Radical Addition via Dual Photoredox/Manganese Catalytic System“. Catalysts 13, Nr. 7 (19.07.2023): 1126. http://dx.doi.org/10.3390/catal13071126.
Der volle Inhalt der QuelleLi, Heng-Hui, Shaoyu Li, Jun Kee Cheng, Shao-Hua Xiang und Bin Tan. „Direct arylation of N-heterocycles enabled by photoredox catalysis“. Chemical Communications 58, Nr. 27 (2022): 4392–95. http://dx.doi.org/10.1039/d2cc01212j.
Der volle Inhalt der QuelleMitsunuma, Harunobu, Hiromu Fuse, Yu Irie, Masaaki Fuki, Yasuhiro Kobori, Kosaku Kato, Akira Yamakata, Masahiro Higashi und Motomu Kanai. „(Invited) Identification of a Self-Photosensitizing Hydrogen Atom Transfer Organocatalyst System“. ECS Meeting Abstracts MA2023-01, Nr. 14 (28.08.2023): 1355. http://dx.doi.org/10.1149/ma2023-01141355mtgabs.
Der volle Inhalt der QuelleDissertationen zum Thema "Photoredox catalytic system"
Fall, Arona. „Donneurs d’électrons organiques : développement d’un nouveau système catalytique photoredox“. Electronic Thesis or Diss., Aix-Marseille, 2021. http://www.theses.fr/2021AIXM0607.
Der volle Inhalt der QuelleDuring this last decade, the reactivity of enamine-based organic electron donor (OED) has been widely explored in electron transfer processes. With exceptionally negative redox potentials, OEDs spontaneously promote single (SET) or double electron transfer (DET) to an organic substrate, to form radical or anionic intermediates. However, the use of stoichiometric amount of OEDs limits their competitivity compared to their organometallic and organic catalysts. This thesis project consisted in developing a new catalytic system with OEDs. Different strategies were envisaged. In a first method a catalytic amount of OED would initiate the electron transfer to reduce the substrate. The oxidation of the generated radical intermediate would allow the regeneration of OED. Unfortunately, this strategy was unsuccessful. The second strategy would consist in regenerating the OED from its air-stable oxidized form OED2+ and a sacrificial electron donor (tertiary amine, sodium dithionite or Rongalite®) under photoactivation. Several optimizing steps allowed the development of a new efficient catalytic photoredox system with the oxidized form as photocatalyst and Rongalite® as sacrificial electron donor. This new photoredox catalytic system was applied to the reduction of various functionals groups (sulfone, aryl halide and triflate) by single electron transfer (SET) and double electron transfer (DET). The reactivity of the photocatalytic system was also explored in radical addition reactions
Buchteile zum Thema "Photoredox catalytic system"
Hill, C. L., und C. M. Prosser-McCartha. „Photocatalytic and Photoredox Properties of Polyoxometalate Systems“. In Catalysis by Metal Complexes, 307–30. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-017-2626-9_10.
Der volle Inhalt der QuelleSubramaniann, H., und M. P. Sibi. „2.12 Asymmetric Catalysis of Radical Reactions“. In Free Radicals: Fundamentals and Applications in Organic Synthesis 2. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-233-00202.
Der volle Inhalt der QuelleHutskalova, V., und C. Sparr. „15.9.4 Synthesis and Applications of Acridinium Salts (Update 2022)“. In Knowledge Updates 2022/1. Stuttgart: Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/sos-sd-115-00850.
Der volle Inhalt der QuelleLambert, Tristan H. „Reactions of Alkenes“. In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0031.
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