dc.contributor.author |
Alan Sheeja, D B |
|
dc.contributor.author |
Mangalam S Nair |
|
dc.date.accessioned |
2014-06-26T05:38:17Z |
|
dc.date.available |
2014-06-26T05:38:17Z |
|
dc.date.issued |
2014 |
|
dc.identifier.citation |
Indian Journal of Chemistry Section B-Organic Chemistry including Medicinal Chemistry 53(3):319-324;Mar 2014 |
en_US |
dc.identifier.issn |
0376-4699 |
|
dc.identifier.uri |
http://ir.niist.res.in:8080/jspui/handle/123456789/1555 |
|
dc.description.abstract |
Curcuma amada Roxb. (Zingiberaceae) rhizomes have been found to be a good source of (E)-labda-8(17),12-diene15,16-dial. This has been chemically transformed to other biologically active compounds like aframodial, zerumin A as well as other natural products like (E)-labda-8(17),12-diene-15,16-olide, 15,16-epoxy-8(17),13(16),14-labdatriene and (-)marginatone. The antimicrobial activity of zerumin A sodium salt as well as other derivatives of the dialdehyde has been established. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
NISCAIR,CSIR |
en_US |
dc.subject |
Curcuma amada |
en_US |
dc.subject |
Zerumin A |
en_US |
dc.subject |
(E)-labda-8(17),12-diene-15,16-dial |
en_US |
dc.subject |
Aframodial |
en_US |
dc.subject |
Antimicrobial |
en_US |
dc.subject |
Chemical transformation |
en_US |
dc.title |
Facile isolation of (E)-labda-8(17),12-diene-15,16-dial from Curcuma amada and its conversion to other biologically active compounds |
en_US |
dc.type |
Article |
en_US |