Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.491783
Title: Synthesis and reactions of new N-heteroaryl boronic acids
Author: Clapham, Kate Mary
ISNI:       0000 0001 3552 0143
Awarding Body: Durham University
Current Institution: Durham University
Date of Award: 2008
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Abstract:
New functionalized pyridazinylboronic acids/esters are reported. A comprehensive study of the reactivity of the C-B bond in palladium-catalyzed cross-couplings with aryl/heteroaryl halides is presented. Aryl/heteroaryl-pyridazines have thereby been obtained in synthetically viable yields (typically 40-75%). A series of pyridazin-3 (2H) - one derivatives have been obtained from the corresponding 3-methoxypyridazines in straightforward procedures. Further functionalization of the pyridazin-3 (2H)-one derivatives through C-C and C-N cross-coupling reactions yielded a number of multiheteroaryl arrays. The synthesis of trifluoromethyl-substituted pyridylboronic acids and pyrazolylboronic esters is described. An extensive study of their palladium-catalyzed cross-couplings with aryl/heteroaryl halides is presented. СF(_3)-substituted aryl/heteroaryl-pyridines have thereby been obtained (51-98% yields). Analogous cross-couplings have yielded heteroaryl-3-(trifluoromethyl)pyrazoles (60-85% yields). Regioselective halogenation of the 4-position of selected trifluoromethylated pyrazole derivatives was successful. Subsequent Suzuki-Miyaura cross-couplings yielded tetra-substituted pyrazolyl derivatives. X-Ray crystal structures are reported for several aryl/heteroaryl-pyridazines and derived pyridazin-3 (2H)-one derivatives, and selected pyridylboronic acids, pyrazolylboronic esters and derived trifluoromethyl-substituted heterobiaryl systems.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.491783  DOI: Not available
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