Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1100
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dc.contributor.authorGOSWAMI, PRITHWISH-
dc.date.accessioned2019-11-18T11:01:48Z-
dc.date.available2019-11-18T11:01:48Z-
dc.date.issued2019-11-15-
dc.identifier.urihttp://hdl.handle.net/123456789/1100-
dc.description.abstractThe research work carried out in this thesis is mainly focused on the organocatalytic and/or Lewis acid catalyzed nucleophilic addition reactions of para-quinone methides and cyclopropenones with various nucleophiles. This thesis is divided into four chapters. Chapter 1 deals with the N-heterocyclic carbene catalyzed synthesis of α-aryl nitriles. Chapter 2 demonstrates a new catalytic activity of bis(amino)cyclopropenylidene (BAC) for the cross vinylogous Rauhut-Currier reaction between enones and p-quinone methides (p-QMs). Chapter 3 involves a 100% atom-economical approach for the synthesis of unsymmetrical diaryl(2-indolyl)methanes through 1,6-conjugate addition of C3-substituted indoles to p quinone methides. Chapter 4 describes a mild organocatalytic approach for the synthesis of O-acylated phenols/alcohols and N-acylated indoles through the ring opening of cyclopropenones with phenols/alcohols and indoles, respectively.en_US
dc.language.isoen_USen_US
dc.publisherIISERMen_US
dc.subjectLewis Aciden_US
dc.subjectOrganocatalyticen_US
dc.subjectNucleophilicen_US
dc.subjectpara-Quinoneen_US
dc.subjectCyclopropenonesen_US
dc.titleOrganocatalytic and Lewis Acid Catalyzed Nucleophilic Addition Reactions of para-Quinone Methides and Cyclopropenonesen_US
dc.typeThesisen_US
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