Constituents of the Roots of Boerhaavia diffusa L: IV: Isolation and Structure Determination of Boeravinones D, E, and F

Chemical and Pharmaceutical Bulletin

Volumn 39, Issue 7, 1991, Pages 1863-1865

  Lami, Nzunzu ^a   Kadota, Shigetoshi ^a   Kikuchi, Tohru ^a  

^a UNIVERSITY OF TOYAMA   (Japan)

Author keywords

12a dehydrorotenoid boeravinone D boeravinone E boeravinone F NMR; Boerhaavia diffusa Nyctaginaceae 6a

Indexed keywords

BENZOPYRAN DERIVATIVE; ROTENOID; UNCLASSIFIED DRUG;

ARTICLE; DRUG ISOLATION; DRUG STRUCTURE; NUCLEAR MAGNETIC RESONANCE; PLANT;

EID: 0025775944     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.39.1863     Document Type: Article

References (7)

1. N. Lami, S. Kadota, T. Kikuchi, and Y. Momose, Chem. Pharm. Bull., 39, 1551 (1991).
2. S. Kadota, N. Lami, Y. Tezuka, and T. Kikuchi, Chem. Pharm. Bull., 37, 3214 (1989); b) Idem,., 38, 1558 (1990).
3. D. Shiengthong, T. Donavanik, V. Uaprasert, S. Roengsumran, and R. A. Nassy-Westropp, Tetrahedron Lett., 1974, 2015.
4. D. G. Carlson, D. Weisleder, and W. H. Tallent, Tetrahedron, 29, 2731 (1973); M. E. Oberholzer, G. J. H. Rall, and D. G. Roux, Phytochemistry, 15, 1283 (1976).
5. J. B. Harborne and T. J. Mabry (ed.), “The Flavonoids: Advances in Research,” Chapman and Hall, London, 1982, pp. 564—576; J. B. Harborne (ed.), “The Flavonoids, Advances in Research Since 1980,” Chapman and Hall, London, 1988, pp. 152—157.
6. I. Messana, F. Ferrari, and A. E. Goulart Sant’Ana, Phytochemistry, 25, 2688 (1986).
7. Hydrochloric acid solution was used in order to separate effectively an alkaloidal component, which was reported to be contained in this plant by Indians workers. However, the content of the alkaloidal component was negligible. See: A. K. Nadkarni, “Dr. K. M. Nadkarni’s Indian Materia Medica,” Vol. 1, A. K. Nadkarni Popular Prakashan Pvt. Ltd., Bombay 1976, pp. 203—205; I. G. Uasi and U. P. Kalintha, J. Inst. Chem., Calcutta, 51, 214 (1979).