Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/30700
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dc.contributor.authorSridhara, M B-
dc.contributor.authorSrinivasa, G R-
dc.contributor.authorGowda, D Channe-
dc.date.accessioned2015-02-27T05:25:18Z-
dc.date.available2015-02-27T05:25:18Z-
dc.date.issued2006-05-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/30700-
dc.description1304-1307en_US
dc.description.abstractA simple and efficient protocol for the chemo-selective reduction of substituted nitroarenes to corresponding anilines in good yields using inexpensive commercial zinc dust and triethylammonium formate in water at ambient temperature and pressure is established. Many other reducible functional groups like methoxy, methyl, ester, nitrile, amide, acid, phenol and halogens are unaltered with the present systems. en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.relation.ispartofseriesInt.CI.8 C 07 Cen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.45B(05) [May 2006]en_US
dc.subjectChemo-selective reductionen_US
dc.subjectNitroarenesen_US
dc.subjectZinc dusten_US
dc.subjectTriethylammonium formateen_US
dc.subjectAmbient temperatureen_US
dc.subjectFunctional groupsen_US
dc.titleFacile water mediated chemo-selective synthesis of anilines from nitroarenes using triethylammonium formateen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.45B(05) [May 2006]

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