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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3384
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dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2021-11-11T11:01:41Z-
dc.date.available2021-11-11T11:01:41Z-
dc.date.issued2012-02-27-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/cr200076q-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3384-
dc.description.abstractN-Hydroxyamidoximes, N-aminoamidoximes, and hydrazidines belong to a class of compounds with the general formula RC═NX(NHY) where X = OH or NH2, Y = OH or NH2, and R is a linear side chain, carbocycle residue, or heterocycle residue. Their structures are similar to those of amidoximes and amidrazones, but they possess very different synthetic utility and pharmacological properties. There are several reviews published on the synthetic and biological applications of amidrazones and amidoximes. (1-8) However, a comprehensive review on the preparative methods, synthetic utility, and biological applications is missing for this class of compounds thus far. We now attempt to readdress the situation by providing a detailed compilation on the chemistry of N-hydroxyamidoximes, N-aminoamidoximes, and hydrazidines in terms of the structure, preparative methods, reactivity, and biological applications.en_US
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectSaltsen_US
dc.subjectAnionsen_US
dc.subjectReaction productsen_US
dc.titleThe Chemistry of N-Hydroxyamidoximes, N-Aminoamidoximes, and Hydrazidinesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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