Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.779994
Title: Nickel-catalyzed arylative cyclizations enabled by reversible alkenylnickel E/Z isomerization
Author: Yap, Connor
ISNI:       0000 0004 7965 6853
Awarding Body: University of Nottingham
Current Institution: University of Nottingham
Date of Award: 2019
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Abstract:
Herein is described the first enantioselective intramolecular allylation of alkenylnickel nucleophiles. These reactions are initiated by the addition of an arylboronic acid across an alkyne, followed by cyclization of the resulting alkenylnickel species onto an allylic phosphate. The reversible E/Z isomerization of the alkenylnickel species is essential for the success of the reactions. This process delivers chiral 1,4-diene-containing hetero- and carbocycles, previously inaccessible via established rhodium catalysis, with excellent levels of regio- and stereocontrol. This reaction further demonstrates the power of reversible alkenylnickel E/Z isomerization in providing products that would otherwise be inaccessible using syn-selective alkyne carbometallation processes. Attempts to extend this reactivity to other classes of electrophilic traps are also described.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.779994  DOI: Not available
Keywords: QD Chemistry
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