Gotowa bibliografia na temat „Photo-cyclisation”

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Artykuły w czasopismach na temat "Photo-cyclisation"

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Shepherd, Nicholas D., Harrison S. Moore, Jonathon E. Beves, and Deanna M. D’Alessandro. "Electrochemical Switching of First-Generation Donor-Acceptor Stenhouse Adducts (DASAs): An Alternative Stimulus for Triene Cyclisation." Chemistry 3, no. 3 (2021): 728–33. http://dx.doi.org/10.3390/chemistry3030051.

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Donor-acceptor Stenhouse adducts (DASAs) are a photo-switch class that undergoes triene cyclisation in response to visible light. Herein, electrochemical oxidation is demonstrated as an effective alternative stimulus for the triene cyclisation commonly associated with photo-switching.
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Blanke, Meik, Jan Balszuweit, Marco Saccone, et al. "Photo-switching and -cyclisation of hydrogen bonded liquid crystals based on resveratrol." Chemical Communications 56, no. 7 (2020): 1105–8. http://dx.doi.org/10.1039/c9cc07721a.

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Leitich, Johannes, Ingeborg Heise, and Kurt Schaffner. "The photo-Nazarov cyclisation of 1-cyclohexenyl-phenyl-methanone revisited." Journal of Photochemistry and Photobiology A: Chemistry 140, no. 3 (2001): 207–13. http://dx.doi.org/10.1016/s1010-6030(01)00417-8.

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SABA, JABBAR, and GUPTA GEETA. "Study of Dissociation Constants of Stobbe Condensation and Cyclisation Products." Journal of Indian Chemical Society Vol. 68, Jan 1991 (1991): 60–61. https://doi.org/10.5281/zenodo.6100714.

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Department of Chemistry, Institute of Science, Nagpur-440 001 <em>Manuscript received 10 April 1990, revised 10 October 1990&nbsp;accepted 28 November 1990</em> In the course of studies of fulgides for their photo chemical properties<sup>1</sup>, studies of their Friedel-Crafts cyclised products<sup>2</sup>, products obtained from cyclation of the diacids (obtained from the hydrolysis of anhydrides) with various cyclisation reagents<sup>3</sup>, and the Stobbe reaction products<sup>4</sup> were studied for their dissociation constants.
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Yamato, Takehiko, Tatsunori Saisyo, Tohru Hironaka, and Shinpei Miyamoto. "Medium-size cyclophanes, 71. Synthesis, structures and photo-induced cyclisation of 1,2-diphenyl[2.n]metacyclophan-1-enes." Journal of Chemical Research 2006, no. 9 (2006): 558–60. http://dx.doi.org/10.3184/030823406778521338.

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Paudel, Arjun, Jian-Yong Hu, and Takehiko Yamato. "Synthesis and structural properties of novel polycyclic aromatic compounds using photo-induced cyclisation of 2,7-di-tert-butyl-4-(phenylethenyl)pyrenes." Journal of Chemical Research 2008, no. 8 (2008): 457–60. http://dx.doi.org/10.3184/030823408x338710.

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Maki, Yoshifumi, Kaoru Shimada, Magoichi Sako, and Kosaku Hirota. "Photo-oxidative cyclisation of 2'-hydroxychalcones leading to flavones induced by heterocycle -oxides : high efficiency of pybimido[54-]pteridine -oxide for the photochemical dehydrogenation." Tetrahedron 44, no. 11 (1988): 3187–94. http://dx.doi.org/10.1016/s0040-4020(01)85950-0.

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Ramesh, C. Kamboj, Dinesh Kumar Pratibha, Sharma Geeta, et al. "Intramolecular cyclisation of photolabile thienylchromenones : synthesis of angular tetracyclic compounds." Journal of Indian Chemical Society Vol. 90, Apr 2013 (2013): 481–87. https://doi.org/10.5281/zenodo.5770350.

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Department of Chemistry, Kurukshetra University, Kurukshetra-136 119, Haryana, India <em>E-mail</em> : rckamboj@rediffmail.com&nbsp; &nbsp; Fax: 91-1744-238277 <em>Manuscript received 12 May 2011, revised 20 March 2012, accepted 07 June 2012</em> Photo-irradiation of 3-alkoxy-2-(thiophen-2-yI)-4H-chromen-4-ones in methanol with Pyrex filtered UV-Iight lead to the formation of interesting angular tetracyclic compounds. In the present study, we demonstrate the formation and distribution of the photoproducts which depends upon the stability of <em>in&nbsp;situ</em> generated 1,4-biradicals (throu
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Gowda, Punith S., Duddu Savaraiah Sharada, and Satyanarayana Gedu. "TBADT Enabled Photo-Induced Radical Cyclization Pathway: A Concise Access to Functionalized Oxindoles." Chemical Communications, 2025. https://doi.org/10.1039/d5cc01590a.

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Herein, this work describes a mild and general protocol for photo-induced cascade cyclisation of arylalkynamides resulting in diversely functionalized oxindoles. This strategy enables the construction of two C−C bonds through...
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Pashley-Johnson, Fred, Rangika Munaweera, Sheikh I. Hossain, et al. "How molecular architecture defines quantum yields." Nature Communications 15, no. 1 (2024). http://dx.doi.org/10.1038/s41467-024-50366-1.

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AbstractUnderstanding the intricate relationship between molecular architecture and function underpins most challenges at the forefront of chemical innovation. Bond-forming reactions are particularly influenced by the topology of a chemical structure, both on small molecule scale and in larger macromolecular frameworks. Herein, we elucidate the impact that molecular architecture has on the photo-induced cyclisations of a series of monodisperse macromolecules with defined spacers between photodimerisable moieties, and examine the relationship between propensity for intramolecular cyclisation an
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Rozprawy doktorskie na temat "Photo-cyclisation"

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Lloyd, Christopher. "The Photo-initiated Bergamn Cyclisation of Z-hex-3-ene-1,5-diyne." Thesis, University of Bristol, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499954.

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Andrieux, Vivien. "Matériaux mous supramoléculaires électro-stimulables obtenus par auto-assemblage de viologènes." Electronic Thesis or Diss., Lyon, École normale supérieure, 2024. http://www.theses.fr/2024ENSL0038.

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L’objectif de cette thèse est de développer des matériaux souples supramoléculaires sensibles aux stimuli électrochimiques. La stratégie de préparation et de stimulation de tels matériaux est basée sur les propriétés d’auto-assemblage d’unités moléculaires dérivés de sels de 4,4-bipyridinium (viologènes). Ce travail de thèse développe en particulier l’étude de la structure, le mécanisme de formation et la stimulation par transfert d’électrons de gels supramoléculaires conducteurs obtenus par auto-assemblage d’un viologène substitué par des groupements cholestéryles. Dans une première partie bi
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