Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/57741
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dc.contributor.authorZeraatpisheh, Fatemeh-
dc.contributor.authorAbadast, Fatemeh-
dc.contributor.authorShahmorad, Maryam-
dc.date.accessioned2021-07-20T06:56:45Z-
dc.date.available2021-07-20T06:56:45Z-
dc.date.issued2021-06-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/57741-
dc.description845-848en_US
dc.description.abstract1-n-Butyl-3-methylimidazolium cyanide ([bmim]CN), in the presence of [bmim]Br has been prepared and used for the first time as the medium as well as reagent for the synthesis of aromatic cyanodienones from the corresponding triarylpyrylium perchlorates by cyanide-halide exchange. The [bmim]CN having a reactive anion, accelerated reaction technique without external solvent renders the whole synthesis into a truly ecofriendly protocol. The products is isolated without aqueous work-up in high purity and excellent yield.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC-B Vol.60B(06) [June 2021]en_US
dc.subjectCyanodienone,en_US
dc.subjecttriarylpyrylium perchlorateen_US
dc.subject1-n-butyl-3-methylimidazolium cyanideen_US
dc.subject1-n-butyl-3-methylimidazolium cyanideen_US
dc.subjectenvironment friendly methodologyen_US
dc.subjectionic liquiden_US
dc.titleRational design and expeditious synthesis of aromatic cyanodienone derivatives assisted by cyanide-halide exchangeen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.60B(06) [June 2021]

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