Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21526
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dc.contributor.authorPardasani, P-
dc.contributor.authorPardasani, R T-
dc.contributor.authorChaturvedi, V-
dc.contributor.authorSaxena, A-
dc.date.accessioned2013-10-04T11:21:13Z-
dc.date.available2013-10-04T11:21:13Z-
dc.date.issued2003-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21526-
dc.description412-415en_US
dc.description.abstractThe reaction of isatin with secondary cyclic α-amino acid 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid gives rise to azomethineylide which undergoes [3+2] cycloaddition with various dipolarophiles to afford inseparable stereoisomeric mixture of spiro oxazolidinone and fused pyrrolidine derivatives. The newly synthesized compounds have been screened for their antimicrobial activities.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(02) [February 2003]en_US
dc.titleStereoisomeric synthesis of oxazolidinone and fused pyrrolidine derivatives via azomethine ylides and their antimicrobial activityen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(02) [February 2003]

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