Absolute configurations of two acyclic triterpenoids from Ekebergia capensis

被引:9
作者
Nishiyama, Y
Moriyasu, M
Ichimaru, M
Kato, A
Mathenge, SG
Nganga, JN
Juma, FD
机构
[1] Kobe Pharmaceut Univ, Dept Nat Med Chem, Higashinada Ku, Kobe, Hyogo 6588558, Japan
[2] Univ Nairobi, Dept Bot, Nairobi, Kenya
[3] Univ Nairobi, Dept Med, Nairobi, Kenya
关键词
Ekebergia capensis; Meliaceae; acyclic triterpenoid; 2,3,22,23-tetrahydroxy-2,6,10,15,19,23-hexamethyl-6,10,14,18-tetracosatetraene; 1,2,3,22,23-pentahydroxy-2,6,10,15,19,23-hexamethyl-6,10,14,18-tetracosatetraene; modified Mosher's method; absolute configuration;
D O I
10.1016/S0031-9422(99)00317-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The absolute configurations of two acyclic triterpenoids 1 and 2, previously isolated from the bark of Ekebergia capensis (Meliaceae) have been determined by the modified Mosher's method. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1593 / 1596
页数:4
相关论文
共 6 条
[1]
HOREAU A, 1962, TETRAHEDRON LETT, V21, P965
[2]
HOREAU A, 1961, TETRAHEDRON LETT, V15, P506
[3]
ELUCIDATION OF THE RELATIVE AND ABSOLUTE STEREOCHEMISTRY OF LOBATRIENE, A MARINE DITERPENE, BY A MODIFIED MOSHER METHOD [J].
KUSUMI, T ;
HAMADA, T ;
ISHITSUKA, MO ;
OHTANI, I ;
KAKISAWA, H .
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (03) :1033-1035
[4]
NGNOKAM D, 1995, NAT PROD LETT, V5, P289
[5]
Acyclic triterpenoids from Ekebergia capensis [J].
Nishiyama, Y ;
Moriyasu, M ;
Ichimaru, M ;
Tachibana, Y ;
Kato, A ;
Mathenge, SG ;
Nganga, JN ;
Juma, FD .
PHYTOCHEMISTRY, 1996, 42 (03) :803-807
[6]
HIGH-FIELD FT NMR APPLICATION OF MOSHER METHOD - THE ABSOLUTE-CONFIGURATIONS OF MARINE TERPENOIDS [J].
OHTANI, I ;
KUSUMI, T ;
KASHMAN, Y ;
KAKISAWA, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (11) :4092-4096