Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46335
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dc.contributor.authorDas, Mrinal K-
dc.contributor.authorChakraborty, Susanta-
dc.date.accessioned2019-03-22T04:39:52Z-
dc.date.available2019-03-22T04:39:52Z-
dc.date.issued1990-04-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46335-
dc.description352-355en_US
dc.description.abstractA series of boron compounds of the general formula [R'(OH)2 has been synthesised by the reaction of trimethoxyboroxine with hydroxamic acids, R'CONROH (R = H, aryl; R' = aryl), in aqueous alcoholic medium. These have been characterized by elemental analyses, UV, IR, NMR (1H and 11B) spectra and molecular weight data. The boron compounds are nonelectrolytes in DMSO and nitromethane. These heterocycles react with oxalic acid, malonic acid, catechol and ethylene glycol to give spiro compounds, which have been characterized.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-A Vol.29A(04) [April 1990]en_US
dc.titleSynthesis and reactivity of some boron heterocycles derived from hydroxamic acidsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.29A(04) [April 1990]

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