Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/9109
Full metadata record
DC FieldValueLanguage
dc.contributor.authorRauf, Abdul-
dc.contributor.authorParveen, Humaira-
dc.date.accessioned2010-05-31T09:49:12Z-
dc.date.available2010-05-31T09:49:12Z-
dc.date.issued2005-06-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/9109-
dc.description1273-1276en_US
dc.description.abstractEsterification of undec-10-enoic acid 1 with 1-(2'-hydroxy-4'-methoxyphenyl)-3-phenyl-prop-2-en-1-ol 2 by using N,N'-dicyclohexylcarbodiimide (DCC) in the presence of 4-(N,N-dimethylamino) pyridine (DMAP) at room temperature, affords 3'-(2''-hydroxy-4''-methoxyphenyl)-1'-phenyl-propenylundec-10-enoate 4. Under similar conditions, compound 1 also reacts with ethylene glycolmonostearate 3 to give the corresponding ester, 1-stearyl-2-undecenyl glycol 5. The fatty alkenoates are characterized on the basis of the elemental analysis and spectral data. All the prepared compounds 4 and 5 and some other fatty alkenoates 6,7,11-13 are tested for their antimicrobial activity.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 C // A 61 P 31/04en_US
dc.sourceIJC-B Vol.44B(06) [June 2005]en_US
dc.titlePreparation, characterization and antimicrobial activity of fatty alkenoatesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(06) [June 2005]

Files in This Item:
File Description SizeFormat 
IJCB 44B(6) 1273-1276.pdf43.6 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.