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Relevant bibliographies by topics / Benzo[b]furan

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Journal articles
Dissertations / Theses
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Conference papers

Academic literature on the topic 'Benzo[b]furan'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Benzo[b]furan"

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Duc, Dau Xuan. "Recent Achievement in the Synthesis of Benzo[b]furans." Current Organic Synthesis 17, no. 7 (2020): 498–517. http://dx.doi.org/10.2174/1570179417666200625212639.

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Background: Benzo[b]furan derivatives are oxygen-containing heterocyclic compounds consisting of fused benzene and furan rings and are present in a large number of natural and non-natural compounds. This class of compounds has a wide spectrum of biological activities, such as antiarrhythmic, anticancer, inflammatory, antioxidant, antimicrobial, and antiviral. Furthermore, benzo[b]furan derivatives have also been applied in various areas, such as organic electroluminescence device materials and organic dyes, photosensitizing material, organic synthesis as building blocks or intermediates. : Bec

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Li, Yibiao, Liang Cheng, Xiaohang Liu, Bin Li, and Ning Sun. "Copper-promoted hydration and annulation of 2-fluorophenylacetylene derivatives: from alkynes to benzo[b]furans and benzo[b]thiophenes." Beilstein Journal of Organic Chemistry 10 (December 4, 2014): 2886–91. http://dx.doi.org/10.3762/bjoc.10.305.

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An efficient copper-promoted hydration reaction and its application in the synthesis of benzo[b]furan and benzo[b]thiophene derivatives is presented starting from readily available 2-fluorophenylacetylene derivatives. The key annulation step involves the hydration of the C–F bond of 2-fluorophenylacetylene derivatives followed by an intramolecular annulation to afford benzo[b]furan and benzo[b]thiophene derivatives. Moreover, structurally important 2,2'-bisbenzofuran scaffolds are provided in good yields.

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Wang, Dezhi, Xi Chen, Hua Yang, et al. "The synthesis of cyclometalated platinum(ii) complexes with benzoaryl-pyridines as C^N ligands for investigating their photophysical, electrochemical and electroluminescent properties." Dalton Transactions 49, no. 44 (2020): 15633–45. http://dx.doi.org/10.1039/d0dt02224a.

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4

Ohta, Akihiro, (the late) Yasuo Akita, Teruya Ohkuwa, et al. "Palladium-catalyze Arylation of Furan, Thiophene, Benzo[b]furan and Benzo[b]thiophene." HETEROCYCLES 31, no. 11 (1990): 1951. http://dx.doi.org/10.3987/com-90-5467.

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Kraľovičová, Eva, Alžbeta Krutošíková, and Jaroslav Kováč. "Preparation and reactions of thieno[3,2-b]furan derivatives." Collection of Czechoslovak Chemical Communications 51, no. 8 (1986): 1685–91. http://dx.doi.org/10.1135/cccc19861685.

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Reactions of 3-(5-aryl-2-furyl)propenoic, 3-(2-benzo[b]furyl)propenoic and 3-(5-ethoxycarbonyl-4H-furo[3,2-b]-2-pyrrolyl)propenoic acids with thionyl chloride in the presence of triethylbenzylammonium chloride were investigated. The obtained 2-arylthieno[3,2-b]-furan-5-carboxylic acid chlorides Ia - Ic and 3-chlorothieno[3,2-b]benzo[b]furan-2-carboxylic acid chloride afforded in substitution nucleophilic reactions the corresponding esters V and carboxylic acids VI which were decarboxylated to VII. 3-Chlorothieno[3,2-b]benzo[b]furan-2-carboxylic acid chloride (Id), 6-ethoxycarbonyl-3-chlorothie

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Arce-Ramos, Lizeth, Juan-Carlos Castillo, and Diana Becerra. "Synthesis and Biological Studies of Benzo[b]furan Derivatives: A Review from 2011 to 2022." Pharmaceuticals 16, no. 9 (2023): 1265. http://dx.doi.org/10.3390/ph16091265.

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The importance of the benzo[b]furan motif becomes evident in the remarkable results of numerous biological investigations, establishing its potential as a robust therapeutic option. This review presents an overview of the synthesis of and exhaustive biological studies conducted on benzo[b]furan derivatives from 2011 to 2022, accentuating their exceptional promise as anticancer, antibacterial, and antifungal agents. Initially, the discussion focuses on chemical synthesis, molecular docking simulations, and both in vitro and in vivo studies. Additionally, we provide an analysis of the intricate

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Chen, Zhi-Cai, Yuan Xie, Yuan-Yuan Yu, Hong-Bin Wu, and Jun-Hua Wan. "A comparative study of the effects of terminal aromatic moieties in spirobifluorene core-based diketopyrrolopyrrole non-fullerene acceptors." New Journal of Chemistry 42, no. 14 (2018): 11854–61. http://dx.doi.org/10.1039/c8nj01549j.

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Fillion, Houda, and Pascal Nebois. "Diels-Alder Reactions of Benzo[b]furan-4,5-diones and Benzo[b]furan-4,7-diones." HETEROCYCLES 50, no. 2 (1999): 1137. http://dx.doi.org/10.3987/rev-98-sr(h)7.

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9

OHTA, A., Y. AKITA, T. OHKUWA, et al. "ChemInform Abstract: Palladium-Catalyzed Arylation of Furan, Thiophene, Benzo(b)furan, and Benzo(b)thiophene." ChemInform 22, no. 14 (2010): no. http://dx.doi.org/10.1002/chin.199114101.

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Váchal, Petr, Pavel Pihera, and Jiří Svoboda. "Thieno[3,2-b]benzofuran - Synthesis and Reactions." Collection of Czechoslovak Chemical Communications 62, no. 9 (1997): 1468–80. http://dx.doi.org/10.1135/cccc19971468.

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Thieno[3,2-b]benzofuran was synthesized starting from benzo[b]furan-3(2H)-one or benzo[b]furan-2-carbaldehyde. Electrophilic substitution reactions such as bromination, formylation, acetylation or nitration, take place in position 2. An electron donating group in position 2 directs further electrophilic substitution into positions 3 and 6, whereas compounds with an electron acceptor in position 2 are substituted exclusively in position 6. Metallation with butyllithium took place in position 2. The 1H and 13C NMR signals of the title compound were fully assigned.

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Dissertations / Theses on the topic "Benzo[b]furan"

1

Friedman, Mark Richard. "Novel thermotropic liquid crystals possessing a benzo[b]furan unit." Thesis, University of Hull, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.342980.

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Liao, Ying-Chi, and 廖英錡. "Pyrolytic Study of 2-(2-Vinylstyryl)furan derivatives and 2-[2-(4-Methoxyphenyl)vinyl]benzo[b]thiophene." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/32400694735627980679.

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碩士<br>國立中山大學<br>化學系研究所<br>94<br>Flash vacuum pyrolysis of 2-(2-vinylstyryl)furan derivatives via electrocyclization followed by dehydrogenation will give 2-(2-naphthalen-2-yl)furan analogues, on the other hand, FVP of 2-(2-vinylstyryl)furan derivatives via electrocyclization followed by [1,5]-H shift will give 3-(2-furyl)-1,2-dihydronaphthalene analogues. FVP of 2-[2-(4-methoxyphenyl)vinyl]benzo[b]thiophene gave three products: trans-4-(2-benzo[b]thiophen-2-ylvinyl)phenol, benzo[b]naphtha[1,2-d]thiophen-2-ol and 1H-6-thiacyclopenta[c]fluorene.

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Ling, Lin Kai, та 林凱苓. "以2,3-benzo[b]furan建構單元之藍色電激發光材料". Thesis, 2005. http://ndltd.ncl.edu.tw/handle/59109238901252549224.

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碩士<br>中國文化大學<br>應用化學研究所<br>93<br>One pot synthesis of benzo[b]furans drivatives with a 2-substituent have been achieved by Pd(0) complex catalyzed Sonogashira coupling reaction of 2-iodophenol with terminal alkynes, followed by cyclization of the internal alkynes formed. These cpompounds possess good solution fluorescence quantum yields, and the emission range from blue to yellow-green. Compound CN-4 is the most thermally stable among all and its decomposition temperature (Td) reaches 360 oC. Except for CN-2 and CN-4 which are amorphous, all other compounds were crystalline. Based on the HOMO

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Liu, Chien-Liang, and 劉健良. "The study in copper(II) chloride-mediated one pot three-step syntheses of benzo[b]furan derivatives and its application for the total synthesis of antimicrobial molecular." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/03492873832870849922.

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碩士<br>國立中興大學<br>化學系所<br>100<br>Copper(II) chloride has been successfully used as the medium to one-pot three-steps synthesis of benzo[b]furan derivatives. A palladium-free and ligand-free reaction condition for Sonogashira- type coupling has been developed, this catalytic system is cheap and easily removed, and provide a good yield. Total synthesis of antimicrobial molecule was accomplished in six steps. This novel route was starting from the 4-methylanisole 64. The iodination of compound 64 by treating with NIS in the presence of TMSCl can provide the 90% yield. After the copper(II) chloride

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Book chapters on the topic "Benzo[b]furan"

1

"4b,5-Dihydro-11H-benzo[b]fluorene (17) to 3,3a-Dihydrophenanthro[4,5-bcd]furan (15)." In Substance Index Cyclic Compounds VIII, Polycyclic Compounds I, edited by Backes, Fröhlich, and Padeken. Georg Thieme Verlag, 2001. http://dx.doi.org/10.1055/b-0035-114406.

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"Synthesis of 2-(Mannopyranosyloxy methyl) Benzo[b] furan through Sonogashira Coupling and Intramolecular Dehydrocyclization." In Carbohydrate Chemistry. CRC Press, 2015. http://dx.doi.org/10.1201/b18400-22.

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Conference papers on the topic "Benzo[b]furan"

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Sharma, Naresh. "Crystal structure analysis of 4-(3′-hydroxy-2′, 3′-dihydro-benzo[b]furan-2-yl)-7-methylcoumarin." In NATIONAL CONFERENCE ON RECENT ADVANCES IN EXPERIMENTAL AND THEORETICAL PHYSICS (RAETP-2018). Author(s), 2018. http://dx.doi.org/10.1063/1.5051291.

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