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dc.contributor.authorGowda, D Channe-
dc.contributor.authorGowda, Shankare-
dc.contributor.authorAbiraj, K-
dc.date.accessioned2013-10-07T10:41:34Z-
dc.date.available2013-10-07T10:41:34Z-
dc.date.issued2003-07-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21664-
dc.description1774-1776en_US
dc.description.abstractAzo compounds, both symmetrical and unsymmetrical are cleaved to amine/s by using Raney nickel and ammonium formate or formic acid in methanol at room temperature. The reductive cleavage is very fast, clean, cost effective and high yielding as compared to earlier methods and many other functionality such as -OH, -CH3 –OCH3, -COOH, -COCH3 and halogen remained unaffected.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(07) [July 2003]en_US
dc.titleRapid cleavage of azo compounds to amine/s using Raney nickel and ammonium formate or formic aciden_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(07) [July 2003]

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