Relevant bibliographies by topics / Acylation of benzofurans

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  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Acylation of benzofurans'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Acylation of benzofurans"

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Camacho-Dávila, Alejandro, José Espinoza-Hicks, Gerardo Zaragoza-Galán, David Chávez-Flores, Víctor Ramos-Sánchez, and Joaquín Tamariz. "A Convergent Total Synthesis of the Biologically Active Benzo­furans Ailanthoidol, Egonol and Homoegonol from Biomass-Derived­ Eugenol." Synthesis 50, no. 17 (2018): 3493–98. http://dx.doi.org/10.1055/s-0037-1610169.

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An efficient, general synthetic protocol for the synthesis of the biologically active benzofurans ailanthoidol, egonol and homoegonol was developed. The key starting material, eugenol, is a naturally occurring and abundant precursor. The protocol, involving sequential acylation and intramolecular Wittig reaction, provides a convenient method for building the benzofuran moiety in good yield.
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2

Zheng, Xuebing, Chuanjun Song, and Yonggang Meng. "New method for the acylation of benzofurans toward the synthesis of 6H-indeno[2,1-b]benzofuran-6-ones and 2,2-bibenzofurans." Arkivoc 2022, no. 5 (2022): 60–69. http://dx.doi.org/10.24820/ark.5550190.p011.624.

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3

Liou, Yan-Cheng, Praneeth Karanam, Yeong-Jiunn Jang, and Wenwei Lin. "Synthesis of Functionalized Benzofurans from para-Quinone Methides via Phospha-1,6-Addition/O-Acylation/Wittig Pathway." Organic Letters 21, no. 19 (2019): 8008–12. http://dx.doi.org/10.1021/acs.orglett.9b03001.

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4

Zhao, Jincan, Hong Fang, Chen Xie, Jianlin Han, Guigen Li, and Yi Pan. "Palladium-Catalyzed C3 Acylation of Benzofurans and Benzothiophenes with Aromatic Aldehydes by Cross-Dehydrogenative Coupling Reactions." Asian Journal of Organic Chemistry 2, no. 12 (2013): 1044–47. http://dx.doi.org/10.1002/ajoc.201300208.

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Mattson, Anita E., та Karl A. Scheidt. "Nucleophilic Acylation ofo-Quinone Methides: An Umpolung Strategy for the Synthesis of α-Aryl Ketones and Benzofurans". Journal of the American Chemical Society 129, № 15 (2007): 4508–9. http://dx.doi.org/10.1021/ja068189n.

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Zhao, Jincan, Hong Fang, Chen Xie, Jianlin Han, Guigen Li, and Yi Pan. "ChemInform Abstract: Palladium-Catalyzed C3 Acylation of Benzofurans and Benzothiophenes with Aromatic Aldehydes by Cross-Dehydrogenative Coupling Reactions." ChemInform 45, no. 18 (2014): no. http://dx.doi.org/10.1002/chin.201418109.

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Gong, Wei-Jie, De-Xian Liu, Fei-Long Li, Jun Gao, Hong-Xi Li та Jian-Ping Lang. "Palladium-catalyzed decarboxylative C3-acylation of benzofurans and benzothiophenes with α-oxocarboxylic acids via direct sp2 C–H bond activation". Tetrahedron 71, № 8 (2015): 1269–75. http://dx.doi.org/10.1016/j.tet.2014.12.095.

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Gong, Wei-Jie, De-Xian Liu, Fei-Long Li, Jun Gao, Hong-Xi Li та Jian-Ping Lang. "ChemInform Abstract: Palladium-Catalyzed Decarboxylative C3-Acylation of Benzofurans and Benzothiophenes with α-Oxocarboxylic Acids via Direct sp2C-H Bond Activation." ChemInform 46, № 26 (2015): no. http://dx.doi.org/10.1002/chin.201526092.

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9

Nunes, Nelson, Ana P. Carvalho, Ruben Elvas-Leitão, et al. "Exploring the Effect of Hierarchical Porosity in BEA Zeolite in Friedel-Crafts Acylation of Furan and Benzofuran." Catalysts 12, no. 9 (2022): 1064. http://dx.doi.org/10.3390/catal12091064.

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Hierarchical BEA zeolite was prepared through desilication or desilication followed by acid treatment. The catalytic performance of BEA zeolite samples was evaluated using Friedel-Crafts acylations with two substrates of different molecular sizes, furan (5.7 Å) and benzofuran (6.9 Å), in the presence of acetic anhydride as acylating agent. The application of the simplified Langmuir-Hinshelwood kinetic model showed that the size of the substrate leads to different catalytic activities, with improved rate constant and turnover frequency (TOF) solely in the presence of benzofuran for both desilic
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10

Wu, Yu-Ran, Shu-Ting Ren, Lei Wang, et al. "Synthesis and AChE inhibitory activity of N-glycosyl benzofuran derivatives." Heterocyclic Communications 25, no. 1 (2019): 162–66. http://dx.doi.org/10.1515/hc-2019-0021.

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AbstractSix N-glycosyl benzofuran derivatives were synthesized by the catalysis of organic bases and condensation agents. The benzofuran derivatives were obtained by the reaction of various salicylaldehydes in acetone, and then hydrolyzed to the corresponding carboxylic acids. Finally, the target compounds were synthesized by acylation and the reaction conditions were optimized. The acetylcholinesterase (AChE) inhibitory activity of the desired compounds was tested using Ellman’s method. Most of the compounds showed acetylcholinesterase-inhibition activity; N-(2,4,5-trihydroxy-6-(hydroxymethyl
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Dissertations / Theses on the topic "Acylation of benzofurans"

1

Richard, Frédéric. "Acylation de composés benzofuraniques en présence de zéolithes." Poitiers, 1997. http://www.theses.fr/1997POIT2266.

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L'acylation du benzofurane et de deux de ses derives (2-methylbenzofurane et 2-acetylbenzofurane) par l'anhydride acetique est realisee avec une bonne selectivite a l'aide de catalyseurs zeolithiques. Dans chaque cas, le produit final peut etre isole selon une methode facile a mettre en uvre. Le catalyseur peut etre recupere, regenere selon la procedure habituelle de pretraitement sous air, et reutilise. Les reactions sont etudiees en presence de diverses zeolithes y et on reporte egalement quelques essais realises en presence d'autres zeolithes (notamment des zeolithes beta). Les reactions so
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Book chapters on the topic "Acylation of benzofurans"

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Richard, F., J. Drouillard, H. Carreyre, J. L. Lemberton, and G. Pérot. "Zeolite catalyzed acylation of heterocyclic aromatic compounds. I—Acylation of benzofuran." In Studies in Surface Science and Catalysis. Elsevier, 1993. http://dx.doi.org/10.1016/s0167-2991(08)63372-8.

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Journal articles
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