1984
DOI: 10.1016/s0031-9422(00)82610-2
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Naphthoquinones and triterpenes from african Diospyros species

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Cited by 70 publications
(27 citation statements)
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“…The plant (9.5 g) was extracted with 300 ml of chloroform by different extraction techniques: static maceration (24h), dynamic maceration (10h + 14h of static maceration), extraction with aid of ultrasonic waves (2h) and extraction in the Soxhlet apparatus at different process duration (2h, 5h, 10h). Chloroform was employed as solvent for these extractions, once it was reported in literature for nafthoquinones extraction (Sidhu and Sankaram 1971, Zhong et al 1984, Pakulski and Budzianowski 1996. All the solutions were evaporated to dryness under reduced pressure.…”
Section: Extracts Preparationmentioning
confidence: 99%
“…The plant (9.5 g) was extracted with 300 ml of chloroform by different extraction techniques: static maceration (24h), dynamic maceration (10h + 14h of static maceration), extraction with aid of ultrasonic waves (2h) and extraction in the Soxhlet apparatus at different process duration (2h, 5h, 10h). Chloroform was employed as solvent for these extractions, once it was reported in literature for nafthoquinones extraction (Sidhu and Sankaram 1971, Zhong et al 1984, Pakulski and Budzianowski 1996. All the solutions were evaporated to dryness under reduced pressure.…”
Section: Extracts Preparationmentioning
confidence: 99%
“…(9) 131.0 C (10) 134.4 C(10), and from HÀC(8) to C(1), C(6), and C(10), as well as the molecular formula of 4 established the planar structure as 3,4,5-trihydroxy-1-tetralone. A NOESY correlation of HÀC(3) with HÀC(4), together with the smaller coupling constants between HÀC(3) and HÀC(4) (2.9 Hz) suggested a cis relationship for the 3,4-diol moiety [17], implying that its absolute configuration could be assigned using the in situ dimolybdenum CD method developed by Snatzkes method [18] [19]. Upon addition of dimolybdenum tetraacetate [Mo 2 (OAc) 4 ] to a solution of 4 in DMSO, a metal complex was generated as an auxiliary chromophore.…”
mentioning
confidence: 95%
“…Naphthoquinones are biologically active naturally occurring compounds found in various plant families, including Avicenniaceae, 7) Acanthaceae, [8][9][10][11] Balsaminaceae, Bignoniaceae, 12,13) Boraginaceae, 14) Droseraceae, 15,16) Ebenaceae, 17,18) Juglandaceae, 19) Lythraceae, Nepenthaceae 20) and Plumbagnaceae. 21,22) The common naphthoquinones found in these plant families are shown in Figs.…”
Section: Naphthoquinones Containing Plants In Thailandmentioning
confidence: 99%