Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692700
Title: Catalytic activation of nitriles towards nucleophilic addition
Author: Lester, Roy P.
ISNI:       0000 0004 5919 5666
Awarding Body: University of Nottingham
Current Institution: University of Nottingham
Date of Award: 2015
Availability of Full Text:
Access through EThOS:
Full text unavailable from EThOS. Restricted access.
Access through Institution:
Abstract:
The work presented in this thesis is focused on the development of a multifaceted approach to the catalytic activation of nitriles. To develop a versatile method for catalytic nitrile activation two probes were utilised; i) the development of a direct synthesis of allylic amides from the corresponding allylic alcohol and nitrile using a commercial platinum salt, together with a detailed mechanistic investigation into the process, ii) the direct synthesis of 2-bezoxazole from the corresponding 2-aminophenol and nitrile with the aid of a commercial platinum salt as well as the use of alcoholic solvents. In addition to nitrile activation a preliminary study on the application and further functionisation of 2-trichlorobenzoxazoles was undertaken. i) A novel multifaceted approach to the direct synthesis of allylic amides via the catalytic activation of di- and trichloroacetonitrile will be discussed. This one-pot methodology relies on the same platinum catalyst to activate a nitrile towards nucleophilic attack of allylic alcohol as well as activate the newly formed allylic imidate towards a [3,3]-sigmatropic rearrangement, which produced a number of allylic amides. In addition to the development of the one-pot allylic amide methodology a number of mechanistic studies including 1H, 13C{1H} and gas chromatography were under taken to better understand the process. ii) The second probe used to identify the versatility of this multifaceted catalyst approach to nitrile activation was the direct synthesis of 2-benzoxazoles. Within this study it was discovered that protic solvents were able to activate di- and trichloroacetonitrile efficiently towards nucleophilic attack of the nitrogen nucleophile. From this discovery a mild and effective synthesis of a variety of di- and trichlorobenzoxazoles was developed in which the solvent was acting as the activating agent towards nucleophilic attack. iii) Preliminary results will also be reported on the novel manipulation of the trichloromethyl moiety of benzoxazoles. Within this study two efficient methodologies for the selective synthesis of 2-(pyrrolidin-1-yl)benzo[d]oxazole and benzo[d]oxazol-2-yl(pyrrolidin-1-yl)methanone were developed from a single starting material. These results show a positive direction for the study into diversity oriented synthesis to form a number of different small molecules from a single starting material by altering the conditions of the reaction.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.692700  DOI: Not available
Keywords: QD241 Organic chemistry
Share: