Synthesis of novel antimicrobial aryl himachalene derivatives from naturally occurring himachalenes

dc.contributor.authorChaudhary, Abha
dc.contributor.authorSood, Swati
dc.contributor.authorDas, Pralay
dc.contributor.authorKaur, Pushpinder
dc.contributor.authorMahajan, Isha
dc.contributor.authorGulati, Arvind
dc.contributor.authorSingh, Bikram
dc.date.accessioned2015-04-20T12:55:43Z
dc.date.available2015-04-20T12:55:43Z
dc.date.issued2014-11-18
dc.description.abstractFive new 2,9,9-trimethyl-6,7,8,9-tetrahydro-benzocyclohepten-5-ylidene-amine derivatives (16a-16e) were synthesized from α-dehydro-ar-himachalene (11) that was originally prepared from an isomeric mixture of α, β and γ himachalenes (10), the abundant sesquiterpenes of Cedrus deodara essential oil. In addition, different aryl himachalenes derivatives (9, 12, 14 and 15) were also formed from 11. The structures of the synthesized compounds were confirmed on the basis of their NMR, IR and mass spectral data. The prepared compounds were tested against a group of sixteen organisms including gram positive and gram negative bacterial and fungal strains. The introduction of a series of substituted imine groups into aryl himachalenes at 5th position (16a-16e) enhanced antimicrobial activity as compared to the aromatized derivatives (9, 12, 14 and 15) against gram-positive bacteria Bacillus subtilis, Micrococcus luteus and Staphylococcus aureus, and mycotoxigenic fungi Aspergillus parasiticus, A. ochraceous and A. sydowii.en
dc.identifier.issn1611-2156
dc.identifier.urihttp://hdl.handle.net/2003/34004
dc.identifier.urihttp://dx.doi.org/10.17877/DE290R-7417
dc.language.isoen
dc.relation.ispartofseriesEXCLI Journal ; Vol. 13, 2014en
dc.subjecthimachalenesen
dc.subjectCedrus deodaraen
dc.subjectessential oilen
dc.subjectantimicrobial activityen
dc.subject.ddc610
dc.titleSynthesis of novel antimicrobial aryl himachalene derivatives from naturally occurring himachalenesen
dc.typeText
dc.type.publicationtypearticle
dcterms.accessRightsopen access
eldorado.dnb.zdberstkatid2132560-1

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