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Relevant bibliographies by topics / Photo-cyclization

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Journal articles

Academic literature on the topic 'Photo-cyclization'

Author: Grafiati

Published: 2 November 2024

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Journal articles on the topic "Photo-cyclization"

1

Zhao, Lishuang, Hongyue Zhang, Jianing Cui, et al. "Photo-induced synthesis and in vitro antitumor activity of Fenestin A analogs." New Journal of Chemistry 41, no. 23 (2017): 14044–48. http://dx.doi.org/10.1039/c7nj03363j.

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2

Yao, Zhuojun, Xueting Wu, Xiaocui Zhang, Qin Xiong, Shichao Jiang та Zhipeng Yu. "Synthesis and evaluation of photo-activatable β-diarylsydnone-l-alanines for fluorogenic photo-click cyclization of peptides". Organic & Biomolecular Chemistry 17, № 28 (2019): 6777–81. http://dx.doi.org/10.1039/c9ob00898e.

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3

Rajeshkumar, Venkatachalam, and Mihaiela C. Stuparu. "A photochemical approach to aromatic extension of the corannulene nucleus." Chemical Communications 52, no. 64 (2016): 9957–60. http://dx.doi.org/10.1039/c6cc04910a.

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4

Connor, Dennis A., Donald R. Arnold, Pradip K. Bakshi, and 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, no. 6 (1995): 762–71. http://dx.doi.org/10.1139/v95-096.

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The photochemical nucleophile–olefin combination, aromatic substitution (photo-NOCAS) reaction of methanol, 2,6-dimethyl-1,6-heptadiene, and 1,4-dicyanobenzene yields three distinct types of 1:1:1 adducts: an acyclic product, 4-(1-methoxymethyl-1,5-dimethyl-5-hexenyl)benzonitrile (8, 5%); a cis–trans pair of cyclohexanes, 4-(3-methoxymethyl-1,3-dimethylcyclohexyl)benzonitrile (9cis (12%) and 9trans (11%)); and a cis–trans pair of cycloheptanes, 4-(4-methoxy-1,4-dimethylcycloheptyl)benzonitrile (10cis (12%) and 10trans (10%)). Variation in the concentration of the nucleophile, methanol, and cod

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5

Chen, Ling, Yu-Ming Cui, Zheng Xu, Jian Cao, Zhan-Jiang Zheng, and 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, no. 74 (2016): 11131–34. http://dx.doi.org/10.1039/c6cc05698a.

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Polycyclic coumarin derivatives were easily prepared by carbocation initiated [4+2] cycloaddition of propargyl silyl ethers with ynamides and fluorescent analysis-oriented photo-irradiated cyclization.

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6

Kim, Kyung-su, You Kyoung Chung, Hyunwoo Kim, Chae Yeon Ha, Joonsuk Huh, and 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, no. 4 (2021): 1969–75. http://dx.doi.org/10.1039/d0ra09581h.

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7

Mizutsu, Ryo, Ryosuke Asato, Colin J. Martin та ін. "Photo-Lewis Acid Generator Based on Radical-Free 6π Photo-Cyclization Reaction". Journal of the American Chemical Society 141, № 51 (2019): 20043–47. http://dx.doi.org/10.1021/jacs.9b11821.

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8

Arnold, Donald R., Kimberly A. McManus, and 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, no. 2 (1994): 415–29. http://dx.doi.org/10.1139/v94-063.

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Irradiation, through Pyrex, of an acetonitrile–methanol (3:1) solution of 1,4-dicyanobenzene (1) and 1,5-hexadiene (9) leads to formation of ortho and meta cyclic adducts (13–16) arising from the intermediate exciplex. There was no evidence for interaction between the two double bonds of this nonconjugated diene. The oxidation potential of 9 is high enough (> 3 V vs. sce) to preclude single electron transfer (SET); no photo-NOCAS products are formed. Similar irradiation of acetonitrile–methanol solutions of 1 and 2-methyl-1,5-hexadiene (10) does yield a photo-NOCAS product (17); reaction oc

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9

Zhou, Zhao-Zhao, Jia-Hui Zhao, Xue-Ya Gou, Xi-Meng Chen, and 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, no. 10 (2019): 1649–54. http://dx.doi.org/10.1039/c9qo00240e.

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Photo-induced radical reductive dehalogenation of inactivated aryl/alkyl bromides and chlorides with a palladium complex is described. Reductive cyclization, dehalogenative deuteration, and radical addition process can be achieved smoothly.

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10

Sun, Bin, Rongcheng Shi, Kesheng Zhang та ін. "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, № 49 (2021): 6050–53. http://dx.doi.org/10.1039/d1cc02415a.

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A green and efficient strategy for the synthesis of quinazolinone derivatives via photo-induced decarboxylative cascade radical acylation/cyclization of unactivated alkenes has been developed under oxidant and photocatalyst free conditions.

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