Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1490
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dc.contributor.authorBhattacharya, Asish K.en_US
dc.contributor.authorKaur, Tanpreeten_US
dc.contributor.authorGANESH, KRISHNA N.en_US
dc.date.accessioned2019-01-21T10:29:25Z
dc.date.available2019-01-21T10:29:25Z
dc.date.issued2010-02en_US
dc.identifier.citationSynthesis, (7).en_US
dc.identifier.issn0039-7881en_US
dc.identifier.issn1437-210Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1490-
dc.identifier.urihttps://doi.org/10.1055/s-0029-1218666en_US
dc.description.abstractThe biologically active natural product, primin and its water-soluble acid analogue, primin acid are prepared in 34% and 25% overall yields, respectively, from a common intermediate using a Grignard reaction and a Johnson-Claisen rearrangement as the key steps.en_US
dc.language.isoenen_US
dc.publisherThieme Publishingen_US
dc.subject1,4-benzoquinonesen_US
dc.subjectPriminen_US
dc.subjectPrimin aciden_US
dc.subjectJohnson-Claisen rearrangementen_US
dc.subject2010en_US
dc.titleSynthesis of the Antibacterial Benzoquinone Primin and its Water-Soluble Analogue, Primin Aciden_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleSynthesisen_US
dc.publication.originofpublisherForeignen_US
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