1956
DOI: 10.1039/jr9560002176
|View full text |Cite
|
Sign up to set email alerts
|

426. Demethoxykanugin: a new crystalline compound from Pongamia glabra

Abstract: Besides kanugin a second crystalline compound has now been isolated from the root as well as the stem bark of Pongamia glabra. By degradation and synthesis i t has been shown to be 3 : 7-dimethoxy-3' : 4'-methylenedioxyflavone and so is demethoxykanugin.THE roots of Poizgamia glabra were examined earlier by Rangaswami, Rao, and Seshadri,l who found therein kanugin ( I a ) and a closely related substance, the latter occurring especially in the thicker roots. Though they obtained kanugin free from the second com… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

1959
1959
2024
2024

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 9 publications
(1 citation statement)
references
References 0 publications
0
1
0
Order By: Relevance
“…On this basis, compound 4 was established as 3,7-dimethoxy-3´4´methylenedioxyflavones and its spectral data were matched with those reported for demethoxykanugin. 15 Compound 5, showed two ortho-coupled aromatic proton doublets at δ 8.17 (1H, d, J = 8.7 Hz) and 7.54 (1H, d, J = 8.7 Hz) in the 1 H NMR spectrum, and were assigned as H-5 and H-6 respectively. Two proton doublets appeared at δ 7.16 (1H, br.…”
Section: Resultsmentioning
confidence: 99%
“…On this basis, compound 4 was established as 3,7-dimethoxy-3´4´methylenedioxyflavones and its spectral data were matched with those reported for demethoxykanugin. 15 Compound 5, showed two ortho-coupled aromatic proton doublets at δ 8.17 (1H, d, J = 8.7 Hz) and 7.54 (1H, d, J = 8.7 Hz) in the 1 H NMR spectrum, and were assigned as H-5 and H-6 respectively. Two proton doublets appeared at δ 7.16 (1H, br.…”
Section: Resultsmentioning
confidence: 99%