Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.251124
Title: Palladium catalysed reactions of halogenated heterocycles
Author: Benmansour, Hadjar
ISNI:       0000 0001 3457 5994
Awarding Body: Durham University
Current Institution: Durham University
Date of Award: 2001
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Abstract:
1- The synthesis of unusually substituted halo-fluoroheterocycles has been achieved. 2,4,6-Tribromo-3,5-difluoropyridine and 4-bromo-2,3,5,6-tetrafluoropyridine were prepared from pentafluoropyridine, aluminium bromide and hydrogen bromide Reactions with lithium halides allowed the preparation of 4-iodo-2,3,5,6- tetrafluoropyridine, 4-iodo-2,6-dibromo-3,5-difluoropyridine, 4-iodo-2,3,5,6- tetrafluoropyridine and 4-chloro-2,6-dibromo-3,5-difluoropyridine.2- Reactions of 2,4,6-tribromo-3, 5-difluoropyridine with nucleophiles showed that selective substitution at the C-F centre can be achieved using hard (sodium ethoxide, phenoxide) nucleophiles.3- Lithium mediated reactions of 2,4,6-tribromo-3,5-difluoropyridine allowed selective functionalisation of the 4-position; lithium-halogen exchange occurred exclusively at this position giving a stable lithium derivative, which was successfully trapped with a range of electrophiles (trimethylsilyl chloride, acid chlorides).4- Palladium mediated couplings of 2,4,6-tribromo-3,5-difluoropyridine with a range of substituted phenylacetylenes was successful and the 2- and 6-positions were the most activated sites. Coupling with boronic acids gave the disubstituted or trisubstituted products; in the case of trisubstitution, all three positions (2-,4- and 6-) were activated towards coupling. 2,4,6-Tribromo-3,5-difluoropyridine formed a stable zinc derivative, which was coupled with iodoaromatics (iodobenzene, diiodobenzene).
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.251124  DOI: Not available
Keywords: NMR spectra Chemistry, Organic
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