1999
DOI: 10.3987/com-99-8679
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Four New Styryllactones form Goniothalamus leiocarpus

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Cited by 45 publications
(37 citation statements)
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“…5) Literature surveys indicated that two major types of bioactive compounds, styryllactones and acetogenins, have been found from Goniothalamus species. In this study, we report herein the isolation and structure elucidation of two new compounds, goniothalesacetate (1) and goniothaesdiol A (2), together with eight known compounds, include three styryllactones, goniodiol-7-monoacetate, 4) goniodiol-8-monoacetate, 4) leiocarpin C, 6) and five alkaloids, liriodenine, 3) griffithazanone A, 7) 4-methyl-2,9,10-(2H)-1-azaanthracencetrione, 7) velutinam 8) and aristolactam BII. 8) Compound 1 was isolated as yellow oil.…”
mentioning
confidence: 99%
“…5) Literature surveys indicated that two major types of bioactive compounds, styryllactones and acetogenins, have been found from Goniothalamus species. In this study, we report herein the isolation and structure elucidation of two new compounds, goniothalesacetate (1) and goniothaesdiol A (2), together with eight known compounds, include three styryllactones, goniodiol-7-monoacetate, 4) goniodiol-8-monoacetate, 4) leiocarpin C, 6) and five alkaloids, liriodenine, 3) griffithazanone A, 7) 4-methyl-2,9,10-(2H)-1-azaanthracencetrione, 7) velutinam 8) and aristolactam BII. 8) Compound 1 was isolated as yellow oil.…”
mentioning
confidence: 99%
“…The similarity of 1 H-and 13 C-NMR spectra of 1 to those of known pyrano-pyrones leiocapin A (3), deoxygoniopypyrone A (4), and (Ϫ)-8-epi-9-deoxygoniopypyrone (5) (Tables 1, 2) showed that 1 had a pyrano-pyrone type skeleton. 12,[16][17][18] The presence of a saturated pyrone ring in 1 was suggested by an IR carbonyl absorption band at 1737 cm Ϫ1 and a slight upfield-shifted carbonyl signal at d C 169.1 ppm (C-3) in the 13 C-NMR spectrum. The heteronuclear single quantum coherence (HSQC) spectrum of 1 showed the direct 1 H- 13 Tables 1 and 2 showed that compound 1 has 1 H-and 13 C-NMR parameters similar to those of compound 5.…”
mentioning
confidence: 99%
“…of NaClO 2 (0.3 g, 3.3 mmol) and NaH 2 PO 4 (0.51 g, 3.3 mmol) in H 2 O (1 ml), was added, and the mixture was stirred at r.t. for 3 h. The solvent was evaporated, the residue was dissolved in AcOEt (5 ml) and washed with H 2 O (5 ml) and brine (5 ml), and dried (Na 2 SO 4 ). Evaporation of the solvent under reduced pressure and purification of the residue by CC (SiO 2 ; 12% AcOEt/hexane) gave 11 (0.34 g, 86% over two steps 2 Cl 2 (3.5 ml), 1H-imidazole (0.25 g, 3.67 mmol) was added at 08, and the mixture was stirred for 5 min; then, TBS-Cl (0.30 g, 2.04 mmol) was added, and the mixture was stirred for 0.5 h at r.t. The mixture was diluted with CH 2 Cl 2 (4 ml), and the org.…”
Section: Experimental Partmentioning
confidence: 99%
“…Styryl lactones are natural products that exhibit significant biological activities such as antitumor, antifungal, and antibiotic properties [1]. Compound 1 was isolated from the stem bark of the tropical plant Goniothalamus leiocarpus [2]. Recently, two syntheses of 1 were reported [3].…”
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confidence: 99%
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