1985
DOI: 10.1246/bcsj.58.2192
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Development and Application of Organic Reagents for Analysis. VI. Synthesis and Fluorescence Spectral Properties of 2-(4-Substituted phenyl)benzofurans

Abstract: A synthesis of fifteen kinds of 2-(4-substituted phenyl)benzofurans (4n) was carried out and their fluorescence spectral properties were investigated concerning their applicability as organic reagents for analyses.

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Cited by 26 publications
(5 citation statements)
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“…Analytical Data for the Suzuki-Miyaura Coupling Products 2-(4'-Methoxyphenyl)pyridine: [19] Colorless solid; 2-(4'-Chlorophenyl)pyridine: [19] Colorless oil; 2-(4'-Nitrophenyl)benzofuran: [22] Yellow solid; 2-(4'-Nitrophenyl)benzothiophene: [23] [25] Colorless oil; …”
Section: Experimental Section General Methodsmentioning
confidence: 99%
“…Analytical Data for the Suzuki-Miyaura Coupling Products 2-(4'-Methoxyphenyl)pyridine: [19] Colorless solid; 2-(4'-Chlorophenyl)pyridine: [19] Colorless oil; 2-(4'-Nitrophenyl)benzofuran: [22] Yellow solid; 2-(4'-Nitrophenyl)benzothiophene: [23] [25] Colorless oil; …”
Section: Experimental Section General Methodsmentioning
confidence: 99%
“…2‐(4′‐Nitrophenyl)benzofuran: 22 Yellow solid; 1 H NMR: δ =8.30 (d, J =8.8 Hz, 2 H), 7.99 (d, J =8.8 Hz, 2 H), 7.64 (d, J =8.0 Hz, 1 H), 7.55 (d, J =8.0 Hz, 1 H), 7.37 (t, J =8.0 Hz, 1 H), 7.30–7.23 (m, 2 H); 13 C NMR: δ =155.4, 153.2, 147.3, 136.3, 128.6, 125.8, 125.2, 124.3, 123.5, 121.6, 111.5, 105.1; MS (EI): m/z =239 (M + , 100%); HR‐MS (EI): m/z = 239.0588, calcd for C 14 H 9 NO 3 (M + ) 239.0583.…”
Section: Methodsmentioning
confidence: 99%
“…A group of researchers reported several kinds of intramolecular cyclization of 2-alkoxyacetophenones (10a) have been described, resulting in 2-R-3-methylbenzofurans (10b). As condensing agents, Na and K alcoholates [61][62][63] or alkalis [64][65][66][67][68] in the polar solvent/environment are being utilized [69,70] as shown in fig. 2j.…”
Section: Cholinesterase Inhibitormentioning
confidence: 99%