Rhodium-catalysed arylative cyclisations of malonate esters by 1,4-rhodium migration
Publication Date
July 17, 2019
Creator
Abstract
Rhodium-catalysed intramolecular arylative cyclisations of malonate esters, generating highly functionalised bicycles has been described. The key step is a known alkenyl-to-aryl 1,4-rhodium migration. The reaction is considered to proceed through regioselective carbometallation of the tethered alkyne, followed by alkenyl-to-aryl 1,4-migration and subsequence intramolecular 1,2-addition to the ester moiety. Discovery and preliminary results were conducted by Dr. S. Karad. Through the use of a bisphosphine base ligand, good levels of enantiocontrol were achieved.
Item Type
ethesis
Thesis Type
MScRes
Supervisors
Subjects (LC)
Associated Schools / Departments
School of Chemistry
eprints ID
55998
UoN Repository URI
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Thesis Corrections.pdf
Type
Full-text
Description
Examined
Size
4.4 MB
Format
Adobe PDF
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