Facile isolation of (E)-labda-8(17),12-diene-15,16-dial from Curcuma amada and its conversion to other biologically active compounds

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DC Field	Value	Language
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
Appears in Collections:	2014

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