Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1230
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dc.contributor.authorTung, Pinku-
dc.contributor.authorRamasastry, S. S. V.-
dc.date.accessioned2019-11-22T12:52:34Z-
dc.date.available2019-11-22T12:52:34Z-
dc.date.issued2019-11-22-
dc.identifier.urihttp://hdl.handle.net/123456789/1230-
dc.description.abstractHere we present an organophosphine catalyzed intramolecular Morita-Baylis-Hillman (IMBH) reaction of biaryl enone-aldehyde. The reaction leads to the formation of cyclohepta- fused biaryls bearing arenes and heteroarenes. The reaction occurs at a mild condition, and the substrates are tolerant of a variety of functional groups. An atroposelective Suzuki reaction can be carried out during the starting material synthesis which can deliver an asymmetric IMBH product of various synthetic utility. Towards this different methods have been employed. However, the methods remain quite ineffective in affording either yield or enantioselectivity. Further study on this aspect is underway.en_US
dc.publisherIISERMen_US
dc.subjectChemistryen_US
dc.subjectOrganophosphine Catalyzeden_US
dc.subjectPlausible Mechanismen_US
dc.subjectOrganophosphine ligandsen_US
dc.subjectAcetonitrileen_US
dc.titleOrganophosphine Catalyzed Intramolecular Morita- Baylis-Hillman Reactionen_US
dc.typeThesisen_US
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