Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775439
Title: Iridium-catalysed borylation of heteroaromatic C-H bonds
Author: Wright, Jay Samuel
ISNI:       0000 0004 7962 6152
Awarding Body: Durham University
Current Institution: Durham University
Date of Award: 2019
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Abstract:
Organoboron compounds are of great importance to organic, medicinal, and materials chemistry, representing key intermediates for the introduction of a wide variety of functional groups. This is best exemplified by the Suzuki-Miyaura cross-coupling reaction. In recent years, the direct C-H borylation of arenes has become an attractive method for the synthesis of aryl boronate esters. However, this transformation is more challenging for heteroarenes bearing an azinyl nitrogen atom, where the presence of the nitrogen lone pair can inhibit the reaction. This is particularly evident at the proximal C-H bond, where C-H activation often does not occur. Whilst many heteroarenes have been investigated, aminopyrazoles remain underexplored. This nucleus features in an array of bioactive molecules, such as herbicides, anti-cancer, and anti-parastic drugs. This thesis presents simple methods for the selective C-H functionalisation of 3- and 5-aminopyrazoles.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.775439  DOI: Not available
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