Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1183
Full metadata record
DC FieldValueLanguage
dc.contributor.authorTung, Pinku-
dc.date.accessioned2019-09-28T13:19:30Z-
dc.date.available2019-09-28T13:19:30Z-
dc.date.issued2019-09-28-
dc.identifier.uriIISERMen_US
dc.identifier.urihttp://hdl.handle.net/123456789/1183-
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.description.sponsorshipIISERMen_US
dc.language.isoenen_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
dc.guideRamasastry, S.S.V.-
Appears in Collections:MS-14

Files in This Item:
File Description SizeFormat 
MS14143.pdfFull Text.pdf7.15 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.