2022
DOI: 10.1016/j.arabjc.2022.104227
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Design, synthesis and biological activity against estrogen receptor-dependent breast cancer of furo[1]benzofuran derivatives

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Cited by 2 publications
(3 citation statements)
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“…52 Earlier methods also involved the treatment of hydroxy-substituted acetophenones/halogen-substituted acetophenones with ketones to attain the synthesis of benzofuran heterocycles. 53,54 Many review articles covering the versatile synthetic approaches for benzofuran synthesis have been published by different research groups. 55, 56 Bhargava et al in 2017 and later Miao et al in 2019 presented reviews on the synthetic pathways toward the synthesis of medicinally important benzofurans and their derivatives.…”
Section: Introductionmentioning
confidence: 99%
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“…52 Earlier methods also involved the treatment of hydroxy-substituted acetophenones/halogen-substituted acetophenones with ketones to attain the synthesis of benzofuran heterocycles. 53,54 Many review articles covering the versatile synthetic approaches for benzofuran synthesis have been published by different research groups. 55, 56 Bhargava et al in 2017 and later Miao et al in 2019 presented reviews on the synthetic pathways toward the synthesis of medicinally important benzofurans and their derivatives.…”
Section: Introductionmentioning
confidence: 99%
“…Considering the medicinal applications of benzofuran derivatives, several methods are reported each year contributing toward their synthesis. Most common methods include the reaction of salicylaldehyde with ethylchloroacetate/ethylbromoacetate or with α-haloketone/acetone . Earlier methods also involved the treatment of hydroxy-substituted acetophenones/halogen-substituted acetophenones with ketones to attain the synthesis of benzofuran heterocycles. , …”
Section: Introductionmentioning
confidence: 99%
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