Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/6461
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMadhusudhan, G-
dc.contributor.authorReddy, G Om-
dc.contributor.authorRamanatham, J-
dc.contributor.authorDubey, P K-
dc.date.accessioned2009-11-05T07:04:03Z-
dc.date.available2009-11-05T07:04:03Z-
dc.date.issued2006-05-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6461-
dc.description1264-1268en_US
dc.description.abstractSynthesis of enantiomerically pure 2-((5R)-2-oxo-5-oxazolidinyl) methyl)-1H-isoindole-1,3(2H)-dione, a key precursor in the preparation of oxazolidinone class of antibacterial agents starting from (S)-epichlorohydrin has been achieved.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl.8 C 07 D // A 61 Pen_US
dc.sourceIJC-B Vol.45B(05) [May 2006]en_US
dc.subjectOxazolidinoneen_US
dc.subjectantibacterialen_US
dc.subjectepichlorohydrinen_US
dc.subjectenantiomerically pureen_US
dc.subjectphthalimideen_US
dc.titleA facile synthesis of 2-((5R)-2-oxo-5-oxazolidinyl)methyl)-1H-isoindole-1,3(2H)-dioneen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(05) [May 2006]

Files in This Item:
File Description SizeFormat 
IJCB 45B(5) 1264-1268.pdf112.96 kBAdobe PDFView/Open


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