Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16737
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dc.contributor.authorThapliyal, PC-
dc.contributor.authorAggarwal, L K-
dc.date.accessioned2013-03-31T14:14:21Z-
dc.date.available2013-03-31T14:14:21Z-
dc.date.issued2000-09-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/16737-
dc.description706-708en_US
dc.description.abstractA study of boron trifluoride etherate catalyzed thermal cross Fries reaction is reported in this paper. Acyl and benzoyl migrations from various aromatic diesters to phenols in dry benzene as solvent takes place selectively and in this way offers an alternative route to the preparation of different hydroxy acetophenones and benzophenones.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.39B(09) [September 2000]en_US
dc.titleThermal cross Fries acyl and benzoyl migrations from aromatic diesters to phenolsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.39B(09) [September 2000]

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