Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/15900
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dc.contributor.authorLokhande, Pradeep D-
dc.contributor.authorWaghmare, Smita R-
dc.contributor.authorGaikwad, Harsh-
dc.contributor.authorHankare, P P-
dc.date.accessioned2013-02-05T19:21:13Z-
dc.date.available2013-02-05T19:21:13Z-
dc.date.issued2013-02-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/15900-
dc.description300-305en_US
dc.description.abstractThe oxidation of aryl methyl ketone and heteroaryl methyl ketone to arylglyoxals and heteroaryl glyoxal respectively has been carried out by using the cheap and easily available, non toxic, Lewis acid CuCl2 in DMSO solvent at 70-80°C within 1-2 hr. The reaction can be performed in air without loss of variety of oxidisable fuctional group like phenolic OH, hetroaryl ring, aryl substituted methyl, halo, nitro group, etc.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.52B(02) [February 2013]en_US
dc.subjectArylen_US
dc.subjectHeteroarylen_US
dc.subjectKetoneen_US
dc.subjectArylglyoxalen_US
dc.subjectHeteroarylglyoxalen_US
dc.subjectCuCl2en_US
dc.subjectDMSOen_US
dc.titleOxidation of aryl and heteroaryl methyl ketone to aryl and heteroarylglyoxals by using CuCl2-DMSOen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.52B(02) [February 2013]

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