Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60106
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dc.contributor.authorSingh, Sushma-
dc.contributor.authorDevi, Poonam-
dc.contributor.authorPundeer, Rashmi-
dc.contributor.authorChaudhri, Vishwas-
dc.date.accessioned2022-07-15T10:52:54Z-
dc.date.available2022-07-15T10:52:54Z-
dc.date.issued2022-07-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60106-
dc.description776-779en_US
dc.description.abstractIn the present study, the utility of the hypervalent iodine(III) reagent, diacetoxyiodobenzene is extended for the efficient synthesis of variously substituted aryl cyanamides. The reaction presents efficient conversion of thioureas to cyanamides under the conditions of ambient temperature while stirring. This organoiodine(III) mediated method features easy isolation of the products and represents an excellent example illustrating thiophilic property of diacetoxyiodobenzene in the desulfurization of thioureas.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.61(07) [July 2022]en_US
dc.subjectDiacetoxyiodobenzeneen_US
dc.subjectDesulfurizationen_US
dc.subjectThiophilicityen_US
dc.subjectAryl thioureaen_US
dc.subjectCyanamideen_US
dc.titleApplication of diacetoxyiodobenzene in the desulfurization of arylthioureasen_US
dc.typeArticleen_US
Appears in Collections:IJC Vol.61(07) [July 2022]

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