Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1615
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dc.contributor.authorKAND, DNYANESHWARen_US
dc.contributor.authorChauhan, Dinesh Pratapsinhen_US
dc.contributor.authorLAHIRI, MAYURIKAen_US
dc.contributor.authorTALUKDAR, PINAKIen_US
dc.date.accessioned2019-02-14T05:00:44Z
dc.date.available2019-02-14T05:00:44Z
dc.date.issued2013-05en_US
dc.identifier.citationChemical Communications ,49(34),en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1615-
dc.identifier.urihttps://doi.org/10.1039/C3CC40824Hen_US
dc.description.abstractSynthesis of both enantiomers of δ-unsaturated γ-amino acids via the enantiodivergent [3,3]-sigmatropic rearrangement strategy is reported. Excellent enantiomeric excess > 94% are observed in the strategy. Cell permeability of a fluorescent amino acid derivative is evaluated by live-cell imaging.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectδ-Unsaturateden_US
dc.subjectγ-amino acidsen_US
dc.subjectCell imaging studiesen_US
dc.subjectEnantiomeric pairsen_US
dc.subject2013en_US
dc.titleδ-Unsaturated γ-amino acids: enantiodivergent synthesis and cell imaging studiesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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