Literatura científica selecionada sobre o tema "Photo-cyclization"
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Artigos de revistas sobre o assunto "Photo-cyclization"
Zhao, Lishuang, Hongyue Zhang, Jianing Cui, Meiqi Zhao, Zhiqiang Wang, Qunfeng Yue e Yingxue Jin. "Photo-induced synthesis and in vitro antitumor activity of Fenestin A analogs". New Journal of Chemistry 41, n.º 23 (2017): 14044–48. http://dx.doi.org/10.1039/c7nj03363j.
Texto completo da fonteYao, Zhuojun, Xueting Wu, Xiaocui Zhang, Qin Xiong, Shichao Jiang e Zhipeng Yu. "Synthesis and evaluation of photo-activatable β-diarylsydnone-l-alanines for fluorogenic photo-click cyclization of peptides". Organic & Biomolecular Chemistry 17, n.º 28 (2019): 6777–81. http://dx.doi.org/10.1039/c9ob00898e.
Texto completo da fonteRajeshkumar, Venkatachalam, e Mihaiela C. Stuparu. "A photochemical approach to aromatic extension of the corannulene nucleus". Chemical Communications 52, n.º 64 (2016): 9957–60. http://dx.doi.org/10.1039/c6cc04910a.
Texto completo da fonteConnor, Dennis A., Donald R. Arnold, Pradip K. Bakshi e T. Stanley Cameron. "Photochemical nucleophile–olefin combination, aromatic substitution (photo-NOCAS) reaction. Part 9: methanol-2,6-dimethyl-1,6-heptadiene, and 1,4-dicyanobenzene". Canadian Journal of Chemistry 73, n.º 6 (1 de junho de 1995): 762–71. http://dx.doi.org/10.1139/v95-096.
Texto completo da fonteChen, Ling, Yu-Ming Cui, Zheng Xu, Jian Cao, Zhan-Jiang Zheng e Li-Wen Xu. "An efficient approach toward formation of polycyclic coumarin derivatives via carbocation-initiated [4+2] cycloaddition and atom-economical photo-irradiated cyclization". Chemical Communications 52, n.º 74 (2016): 11131–34. http://dx.doi.org/10.1039/c6cc05698a.
Texto completo da fonteKim, Kyung-su, You Kyoung Chung, Hyunwoo Kim, Chae Yeon Ha, Joonsuk Huh e Changsik Song. "Additive-free photo-mediated oxidative cyclization of pyridinium acylhydrazones to 1,3,4-oxadiazoles: solid-state conversion in a microporous organic polymer and supramolecular energy-level engineering". RSC Advances 11, n.º 4 (2021): 1969–75. http://dx.doi.org/10.1039/d0ra09581h.
Texto completo da fonteMizutsu, Ryo, Ryosuke Asato, Colin J. Martin, Mihoko Yamada, Yoshiko Nishikawa, Shohei Katao, Miku Yamada, Takuya Nakashima e Tsuyoshi Kawai. "Photo-Lewis Acid Generator Based on Radical-Free 6π Photo-Cyclization Reaction". Journal of the American Chemical Society 141, n.º 51 (8 de dezembro de 2019): 20043–47. http://dx.doi.org/10.1021/jacs.9b11821.
Texto completo da fonteArnold, Donald R., Kimberly A. McManus e Xinyao Du. "Photochemical nucleophile–olefin combination, aromatic substitution (photo-NOCAS) reaction. Part 6: methanol, nonconjugated dienes, and 1,4-dicyanobenzene". Canadian Journal of Chemistry 72, n.º 2 (1 de fevereiro de 1994): 415–29. http://dx.doi.org/10.1139/v94-063.
Texto completo da fonteZhou, Zhao-Zhao, Jia-Hui Zhao, Xue-Ya Gou, Xi-Meng Chen e Yong-Min Liang. "Visible-light-mediated hydrodehalogenation and Br/D exchange of inactivated aryl and alkyl halides with a palladium complex". Organic Chemistry Frontiers 6, n.º 10 (2019): 1649–54. http://dx.doi.org/10.1039/c9qo00240e.
Texto completo da fonteSun, Bin, Rongcheng Shi, Kesheng Zhang, Xiaoli Tang, Xiayue Shi, Jiayun Xu, Jin Yang e Can Jin. "Photoinduced homolytic decarboxylative acylation/cyclization of unactivated alkenes with α-keto acid under external oxidant and photocatalyst free conditions: access to quinazolinone derivatives". Chemical Communications 57, n.º 49 (2021): 6050–53. http://dx.doi.org/10.1039/d1cc02415a.
Texto completo da fonteTeses / dissertações sobre o assunto "Photo-cyclization"
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.
Texto completo da fonteThe aim of this thesis is to develop electron-responsive supramolecular soft-materials. The strategy for the preparation and stimulation of such materials is based on the self-assembly properties of molecular units derived from 4,4-bipyridinium salts (viologens). The thesis research work carried has been focused on the structural characterizations, the study of gelation mechanism and the stimulation (electrochemical reduction or photo-reduction) of conductive gels obtained through the self-assembly of a cholesteryl substituted viologen. A first bibliographic part will describe the principal features of supramolecular gels, the challenges related to their characterization and electric stimulation and the potential of viologen-based supramolecular gels for the development of new electron-responsive supramolecular gels. The second part of the manuscript is devoted to present the experimental work performed for the synthesis, the formulation and the characterizations that led to the design of a conductive viologen-based supramolecular gel exhibiting ideal properties for electrochemical stimulation and in situ monitoring. The stimulation of conductive viologen gels, consisting in the electrochemical reduction or photoreduction are described in a third part. This part describes in details the different strategies used to reach an efficient reduction of the viologen moieties which are entrapped in the gel supramolecular network. This work demonstrates that the studied viologen gel is one of the very first systems able to undergo reversible electrochemically induced supramolecular polymerization and de-polymerization
張文昇. "Photo-cyclization of a-iodo cycloalkanones bearing an allenic side chain". Thesis, 2001. http://ndltd.ncl.edu.tw/handle/56860367154407452025.
Texto completo da fonte國立清華大學
化學系
89
The main goal of the synthesis is to study the Photo-induced cyclization reaction of α- iodo cycloalkanones bearing an allenic side chain. We first use the α- iodo cycloalkanone compound 71a-b as starting material, introduce the side chain of allene from β-position successfully by 1,4-Michael addition and then follow with Photo-induced Electron Transfer(PET) cyclization reaction, we obtain the 5、5-fused, 6、5-fused bicycle compounds 73a-b and 74a-c. Besides, we compare the difference of reaction by using Iodide and Slow-addition radical cyclization. From the results, we conclude that the products are all the same. It is avoidable to use the reagent that generate radical because of the allenic side chain can proceed the Photo-induced Electron Transfer cyclization reaction. It is also more convenient of purification. We can construct the structure of 5、5-fused and 6、5-fused bicycle compounds efficient and take advantage of in the synthesis of natural compounds such as (+)-Axamide-4 or (+)-Axisonitrile-4.