2 NEW FLAVONES FROM EUPATORIUM-COELESTINUM

被引：28

作者：

LEVAN, N ^{[1
]}

PHAM, TVC ^{[1
]}

机构：

[1] LOUISIANA STATE UNIV,DEPT CHEM,BATON ROUGE,LA 70803

来源：

PHYTOCHEMISTRY | 1979年 / 18卷 / 11期

关键词：

Compositae; Eupatorieae; Eupatorium coelestinum; new flavones;

D O I：

10.1016/0031-9422(79)83070-8

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Besides coumarin, nobiletin, lucidin dimethyl ether and 5,6,7,3′,4′-pentamethoxyflavone, two new highly oxygenated flavones were isolated from Eupatorium coelestinum. Their structures were determined by spectroscopic methods and alkaline degradations as 5,6,7,8,3′,4′,5′ -heptamethoxyflavone and 5,6,7,8,5′-pentamethoxy-3′,4′-methylenedioxyflavone. © 1979.

引用

页码：1859 / 1861

页数：3

共 16 条

[1] Synthesis derivatives of myristicin.
Baker, W
Montgomery, LV
Smith, HA
[J]. JOURNAL OF THE CHEMICAL SOCIETY, 1932, : 1281 - 1283
[2] Derivatives of Pentahydroxybenzene, and a synthesis of pedicellin
Baker, W
[J]. JOURNAL OF THE CHEMICAL SOCIETY, 1941, : 662 - 670
[3] NOBILETIN IS MAIN FUNGISTAT IN TANGERINES RESISTANT TO MAL SECCO
BENAZIZ, A
[J]. SCIENCE, 1967, 155 (3765) : 1026 - +
[4] BORN R, 1960, CHEM IND-LONDON, P264
[5] CHOWDHURY BK, 1971, J INDIAN CHEM SOC, V48, P80
[6] DERIVATIVES OF METHYLENEDIOXY-BENZENE .24. SYNTHESIS OF O-SAFROLE AND OF MYRISTICINE
DALLACKE.F
SLUYSMAN.R
[J]. MONATSHEFTE FUR CHEMIE, 1969, 100 (02): : 560 - &
[7] DOMINGUEZ XA, 1977, BIOL CHEM COMPOSITAE, P487
[8] CHEMOTAXONOMY OF RUTACEAE .4. CONSTITUENTS OF MURRAYA PANICULATA (LINN) JACK
DREYER, DL
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1968, 33 (09) : 3574 - &
[9] HORII Z, 1940, J PHARM CHEM JAPAN, V60, P614
[10] SYNTHESES OF FLAVONES FROM LINDERA LUCIDA
LEE, HH
TAN, CH
[J]. JOURNAL OF THE CHEMICAL SOCIETY, 1965, (APR): : 2743 - &

← 1 2 →