Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/835
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dc.contributor.authorSingh, Gurdeep-
dc.date.accessioned2017-07-18T07:31:20Z-
dc.date.available2017-07-18T07:31:20Z-
dc.date.issued2017-07-18-
dc.identifier.urihttp://hdl.handle.net/123456789/835-
dc.description.abstractBis-(dialkylamino)-cyclopropenylidene (BAC) has been utilized as a BrĂ˜nsted base for the conjugate addition of C-nucleophiles to para-quinone methides and chalcones. This transformation occurs at mild conditions and is tolerant to a variety of functional groups. This protocol provides an easy and straightforward access to a set of diaryl and triarylmethanes in good to excellent yieldsen_US
dc.description.sponsorshipIISER-Men_US
dc.language.isoenen_US
dc.publisherIISER-Men_US
dc.subjectChemistryen_US
dc.subjectNuleophilesen_US
dc.subjectp-quinone methidesen_US
dc.subjectBis-(dialkylamino)-cyclopropenylideneen_US
dc.subjectChalconesen_US
dc.titleBis-(dialkylamino)-cyclopropenylidene (BAC) Catalyzed Conjugate Addition of Nuleophiles to Para-Quinone Methides and Chalconesen_US
dc.typeThesisen_US
dc.guideAnand, R.V.-
Appears in Collections:MS Dissertation by MP-2014

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