Добірка наукової літератури з теми "Photoredox catalytic system"
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Статті в журналах з теми "Photoredox catalytic system"
Yang, Qiong, Fengqian Zhao, Na Zhang, Mingke Liu, Huanhuan Hu, Jingjie Zhang, and Shaolin Zhou. "Mild dynamic kinetic resolution of amines by coupled visible-light photoredox and enzyme catalysis." Chemical Communications 54, no. 100 (2018): 14065–68. http://dx.doi.org/10.1039/c8cc07990k.
Повний текст джерелаLeadbeater, Nicholas, Jyoti Nandi, and Mason Witko. "Combining Oxoammonium Cation Mediated Oxidation and Photoredox Catalysis for the Conversion of Aldehydes into Nitriles." Synlett 29, no. 16 (September 12, 2018): 2185–90. http://dx.doi.org/10.1055/s-0037-1610272.
Повний текст джерелаTlahuext-Aca, Adrian, Matthew N. Hopkinson, Basudev Sahoo, and Frank Glorius. "Dual gold/photoredox-catalyzed C(sp)–H arylation of terminal alkynes with diazonium salts." Chemical Science 7, no. 1 (2016): 89–93. http://dx.doi.org/10.1039/c5sc02583d.
Повний текст джерелаHu, Xia, Guoting Zhang, Faxiang Bu, Xu Luo, Kebing Yi, Heng Zhang, and Aiwen Lei. "Photoinduced oxidative activation of electron-rich arenes: alkenylation with H2 evolution under external oxidant-free conditions." Chemical Science 9, no. 6 (2018): 1521–26. http://dx.doi.org/10.1039/c7sc04634k.
Повний текст джерелаHossain, Asik, Aditya Bhattacharyya, and Oliver Reiser. "Copper’s rapid ascent in visible-light photoredox catalysis." Science 364, no. 6439 (May 2, 2019): eaav9713. http://dx.doi.org/10.1126/science.aav9713.
Повний текст джерелаNaumann, Robert, Christoph Kerzig, and Martin Goez. "Laboratory-scale photoredox catalysis using hydrated electrons sustainably generated with a single green laser." Chem. Sci. 8, no. 11 (2017): 7510–20. http://dx.doi.org/10.1039/c7sc03514d.
Повний текст джерелаPagire, Santosh K., Naoya Kumagai та 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, № 20 (2020): 5168–74. http://dx.doi.org/10.1039/d0sc01890b.
Повний текст джерелаKostromitin, Vladislav S., Vitalij V. Levin, and Alexander D. Dilman. "Atom Transfer Radical Addition via Dual Photoredox/Manganese Catalytic System." Catalysts 13, no. 7 (July 19, 2023): 1126. http://dx.doi.org/10.3390/catal13071126.
Повний текст джерелаLi, Heng-Hui, Shaoyu Li, Jun Kee Cheng, Shao-Hua Xiang, and Bin Tan. "Direct arylation of N-heterocycles enabled by photoredox catalysis." Chemical Communications 58, no. 27 (2022): 4392–95. http://dx.doi.org/10.1039/d2cc01212j.
Повний текст джерелаMitsunuma, Harunobu, Hiromu Fuse, Yu Irie, Masaaki Fuki, Yasuhiro Kobori, Kosaku Kato, Akira Yamakata, Masahiro Higashi, and Motomu Kanai. "(Invited) Identification of a Self-Photosensitizing Hydrogen Atom Transfer Organocatalyst System." ECS Meeting Abstracts MA2023-01, no. 14 (August 28, 2023): 1355. http://dx.doi.org/10.1149/ma2023-01141355mtgabs.
Повний текст джерелаДисертації з теми "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.
Повний текст джерелаDuring 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
Частини книг з теми "Photoredox catalytic system"
Hill, C. L., and 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.
Повний текст джерелаSubramaniann, H., and 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.
Повний текст джерелаHutskalova, V., and 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.
Повний текст джерелаLambert, 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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