Gotowa bibliografia na temat „Photoredox catalytic system”
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Artykuły w czasopismach na temat "Photoredox catalytic system"
Yang, Qiong, Fengqian Zhao, Na Zhang, Mingke Liu, Huanhuan Hu, Jingjie Zhang i 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.
Pełny tekst źródłaLeadbeater, Nicholas, Jyoti Nandi i 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.
Pełny tekst źródłaTlahuext-Aca, Adrian, Matthew N. Hopkinson, Basudev Sahoo i 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.
Pełny tekst źródłaHu, Xia, Guoting Zhang, Faxiang Bu, Xu Luo, Kebing Yi, Heng Zhang i 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.
Pełny tekst źródłaHossain, Asik, Aditya Bhattacharyya i Oliver Reiser. "Copper’s rapid ascent in visible-light photoredox catalysis". Science 364, nr 6439 (2.05.2019): eaav9713. http://dx.doi.org/10.1126/science.aav9713.
Pełny tekst źródłaNaumann, Robert, Christoph Kerzig i 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.
Pełny tekst źródłaPagire, Santosh K., Naoya Kumagai i 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.
Pełny tekst źródłaKostromitin, Vladislav S., Vitalij V. Levin i 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.
Pełny tekst źródłaLi, Heng-Hui, Shaoyu Li, Jun Kee Cheng, Shao-Hua Xiang i 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.
Pełny tekst źródłaMitsunuma, Harunobu, Hiromu Fuse, Yu Irie, Masaaki Fuki, Yasuhiro Kobori, Kosaku Kato, Akira Yamakata, Masahiro Higashi i 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.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaDuring 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
Części książek na temat "Photoredox catalytic system"
Hill, C. L., i C. M. Prosser-McCartha. "Photocatalytic and Photoredox Properties of Polyoxometalate Systems". W Catalysis by Metal Complexes, 307–30. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-017-2626-9_10.
Pełny tekst źródłaSubramaniann, H., i M. P. Sibi. "2.12 Asymmetric Catalysis of Radical Reactions". W 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.
Pełny tekst źródłaHutskalova, V., i C. Sparr. "15.9.4 Synthesis and Applications of Acridinium Salts (Update 2022)". W Knowledge Updates 2022/1. Stuttgart: Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/sos-sd-115-00850.
Pełny tekst źródłaLambert, Tristan H. "Reactions of Alkenes". W Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0031.
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