Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16638
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dc.contributor.authorSingh, Sundaram-
dc.contributor.authorShukla, Ajay Kumar-
dc.contributor.authorSingh, Krishna Nand-
dc.date.accessioned2013-03-29T19:58:01Z-
dc.date.available2013-03-29T19:58:01Z-
dc.date.issued1999-10-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/16638-
dc.description1184-1188en_US
dc.description.abstractTetraethylammonium  superoxide, generated in  situ  by the phase transfer reaction of potassium superoxide and tetraethylammonium bromide, brings about a clean cleavage of various anhydrides. particularly those with high molecular weight in dry dimethylformamide. As an outcome, succinic anhydride 1; glutaric anhydride 2; 3;3-dimethylglutaric anhydride 3;phthalic anhydride 4; diphenic anhydride 5; 1,2,3,4-tetrahydro-9-oxo-1 ,4-ethanonaphthalene-2,3-endo-dicarboxylic anhydride 6; 1,4,5,6,7,7-hexachloro-5-norbornene-2,3-dicarboxylic anhydride 7; endo-bicyclo [2.2.1] heptan-2-one-5,6- dicarboxylic  anhydride 8: cis-5 -norbornene-endo-2,3-dicarboxylic anhydride 9 and trans-1,2-cyclohexane dicarboxylic anhydride 10 have been transformed into their corresponding dicarboxylic acids in fairly good yields. The report demonstrates the applicability of tetraethylammonium bromide as a phase transfer catalyst for efficient superoxide studiesen_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.38B(10) [October 1999]en_US
dc.titlePhase transfer catalysis by tetraethylammonium bromide: Nucleophilic opening of anhydrides using potassium superoxide in aprotic mediumen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(10) [October 1999]

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