1987
DOI: 10.1021/np50052a033
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Two New Flavones in Citrus reticulata

Abstract: To compare the difference of constituents in the pericarp and in the leaf of Citrus species, polyoxygenated flavones were examined using the leaves of Citrus reticulata Blanco (Rutaceae). Two new flavones, which were not detected in the pericarps of the plant, were isolated, along with other polyoxygenated flavones (1). In this paper the structure elucidation and the syntheses of the flavones are described.Besides eight known polyoxygenated flavones (5-hydroxy-3',4',

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Cited by 12 publications
(3 citation statements)
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“…+ at m/z = 481 and 1 H NMR spectrum was compatible with that reported in literature [19]. A solution of 3-benzyloxy-29-hydroxy-39,4,49,59,69-pentamethoxylchalcone (192 mg) in ethanol (10 mL) containing 50 mg of H 3 PO 4 was heated to reflux for 16 h. Upon concentration, the resultant mixture was mixed with water and extracted twice with ethyl acetate (50 mL62).…”
Section: Lrms For C 27 H 28 O 8 (M+h)supporting
confidence: 90%
“…+ at m/z = 481 and 1 H NMR spectrum was compatible with that reported in literature [19]. A solution of 3-benzyloxy-29-hydroxy-39,4,49,59,69-pentamethoxylchalcone (192 mg) in ethanol (10 mL) containing 50 mg of H 3 PO 4 was heated to reflux for 16 h. Upon concentration, the resultant mixture was mixed with water and extracted twice with ethyl acetate (50 mL62).…”
Section: Lrms For C 27 H 28 O 8 (M+h)supporting
confidence: 90%
“…The known compounds were fully characterized as scoparone (4), scopoletin (5), nobiletin (6), 8) sinensetin (7), 8) tangeretin (8), 8) 5-hydroxy-6,7,8,4Ј-tetramethoxyflavone (9), 9) 5-hydroxy-6,7,3Ј,4Ј-tetramethoxyflavone (10), 10,11) 5-demethylnobiletin (11), 9,12) 6-demethoxynobiletin (12), 8) 6-demethoxytangeretin (13), 8) 5,6,7,4Ј-tetramethoxyflavone (14), 13,14) 3,5,6,7,3Ј,4Ј-hexamethoxyflavone (15), 15,16) 3Ј-hydroxy-5,6,7,8,4Ј-pentamethoxyflavone (16), 17) 3,5,6,7,8,3Ј,4Ј-heptamethoxyflavone (17), 8) 7-hydroxy-5,6,3Ј,4Ј-tetramethoxyflavone (18), 17) 7-hydroxy-5,6,8,3Ј,4Ј-pentamethoxyflavone (19), 18) 5,7,8,3Ј,4Ј-pentamethoxyflavanone (20), 19) 5-Odemethylcitromitin (21), 20) 3,4,3Ј,4Ј,5Ј,6Ј-hexamethoxy-2Ј-hydroxychalcone (22), 21) 2Ј-hydroxy-4,4Ј,5Ј,6Ј-tetramethoxychalcone (23) 22,23) and b-sitosterol (24) by direct comparison with authentic samples and/or spectral data reported in the literature.…”
mentioning
confidence: 99%
“…As cromatografias de coluna e de camada delgada são geralmente usados em estudos quantitativos para alguns dos compostos fenólicos em citros (Albach & Redman, 1969;Albach et al, 1981;Mizuno et al, 1987;Tomas et al, 1978).…”
Section: Compostos Fenólicos Em Citrosunclassified