Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21488
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dc.contributor.authorMaheshwari, Anjana-
dc.contributor.authorGoswami, Lalit N-
dc.contributor.authorDikshit, Dinesh K-
dc.contributor.authorJoshi, B S-
dc.contributor.authorRoy, Raja-
dc.date.accessioned2013-10-04T10:23:26Z-
dc.date.available2013-10-04T10:23:26Z-
dc.date.issued2003-01-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21488-
dc.description154-158en_US
dc.description.abstractα-Bromination of the cyclically protected S-pyroglutamic acid, its subsequent reactions with nucleophillic reagents via corresponding N-acylimminium intermediate is described.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(01) [January 2003]en_US
dc.titleImminium ion chemistry at C-2 of pyroglutamates: Unexpected formation of 1,4- Methano-3-oxa-6-t-butyl-7 -azabicyc1o[7.3.0]decan-2,8-dione†en_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(01) [January 2003]

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