Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/8941
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dc.contributor.authorMadhusudhan, G-
dc.contributor.authorReddy, G Om-
dc.contributor.authorRamanatham, J-
dc.contributor.authorDubey, P K-
dc.date.accessioned2010-05-14T11:15:49Z-
dc.date.available2010-05-14T11:15:49Z-
dc.date.issued2005-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/8941-
dc.description366-371en_US
dc.description.abstractNovel syn-N-arylsulfonyl-4-substituted phenyl-2-oxo-1,3-oxazolidine-5-carboxylates have been synthesized from the corresponding -azido alcohols and converted to their anti-form by epimerizing C-2 proton using DBU. Studies on the stabilization energies are done to evaluate conversion from syn-to anti-and not the vice-versa. All the compounds have been tested for their in vitro anti-bacterial activity against S. aureus, E. faecalis and E. faecium.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.7 C 07 D 263/00 // A 61 P 31/04en_US
dc.sourceIJC-B Vol.44B(02) [February 2005]en_US
dc.titleSynthesis of syn-N-aryl sulfonyl-4-substituted phenyl-2-oxo-1,3-oxazolidine-5-carboxylates and their conversion to ant-form using DBUen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.44B(02) [February 2005]

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