An investigation of the enzymatic kinetic resolution of Morita-Baylis-Hillman adducts and their further functionalisation

A thesis submitted to the Faculty of Science University of the Witwatersrand Johannesburg in fulfilment of the requirements for the degree of Doctor of Philosophy, July 2019 The Morita-Baylis-Hillman reaction (MBHR) is a carbon-carbon bond forming reaction that affords multifunctional Morita-Baylis-...

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Main Author: Juma, Wanyama Peter
Format: Thesis
Language:English
Published: 2019
Subjects:
Online Access:https://hdl.handle.net/10539/29573
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spelling ftunivwitwaters:oai:wiredspace.wits.ac.za:10539/29573 2023-06-11T04:06:43+02:00 An investigation of the enzymatic kinetic resolution of Morita-Baylis-Hillman adducts and their further functionalisation Juma, Wanyama Peter 2019 Online resource (x, 323 leaves) application/pdf https://hdl.handle.net/10539/29573 en eng Juma, Peter Wanyama, (2019) An investigation of the enzymatic kinetic resolution of Morita-Baylis-Hillman adducts and their further functionalisation, University of the Witwatersrand, Johannesburg, https://hdl.handle.net/10539/29573 https://hdl.handle.net/10539/29573 Organic compounds--Synthesis Chemical reactions Thesis 2019 ftunivwitwaters 2023-05-15T09:57:46Z A thesis submitted to the Faculty of Science University of the Witwatersrand Johannesburg in fulfilment of the requirements for the degree of Doctor of Philosophy, July 2019 The Morita-Baylis-Hillman reaction (MBHR) is a carbon-carbon bond forming reaction that affords multifunctional Morita-Baylis-Hillman adducts (MBHA) with various synthetic applications. Unfortunately, many of the synthetic applications of these adducts cannot be realised because these adducts are formed in racemic form. This thesis has investigated functionalisation of enantiopure MBHA obtained using biocatalytic methods. The first part of the thesis describes the use of enantiopure aldehydes N-Boc-L-phenylalaninal and N-Boc-D-phenylalaninal to synthesize several Morita-Baylis-Hillman adducts in order to obtain diastereomers that would be separable by chromatographic methods. Unfortunately, this approach proved unsuccessful due to racemization of the aldehydes or MBHA under the reaction conditions applied. The second approach described is the resolution of racemic MBH acetates and esters using different enzymes. This exercise led to the identification of several lipases that were able to resolve racemic MBH acetates with excellent enantiomeric excess (ee) values and enantiomeric ratios (E). Racemic MBH adducts derived from the reaction of acrylonitrile with benzaldehyde, cinnamaldehyde and hydrocinnamaldehyde were successfully resolved. In each case the (+)-alcohol products were isolated in 94 - 97% ee after lipase-mediated enzymatic kinetic resolution of the corresponding acetates. Mosher’s ester derivatisation protocol was used to determine the absolute configuration of the resolved adducts, which was found to be (S). A lipase from Pseudomonas fluorescens, and Candida antarctica type B were found to be the best-performing enzymes. The last part of the thesis investigated the use of nitrogen nucleophiles for Michael addition to MBH adducts. The process confirmed that the use of nitrogen nucleophiles on TBS protected MBH adducts afforded ... Thesis Antarc* Antarctica University of the Witwatersrand, Johannesburg: WITS Institutional Repository on DSpace (WIReDSpace)
institution Open Polar
collection University of the Witwatersrand, Johannesburg: WITS Institutional Repository on DSpace (WIReDSpace)
op_collection_id ftunivwitwaters
language English
topic Organic compounds--Synthesis
Chemical reactions
spellingShingle Organic compounds--Synthesis
Chemical reactions
Juma, Wanyama Peter
An investigation of the enzymatic kinetic resolution of Morita-Baylis-Hillman adducts and their further functionalisation
topic_facet Organic compounds--Synthesis
Chemical reactions
description A thesis submitted to the Faculty of Science University of the Witwatersrand Johannesburg in fulfilment of the requirements for the degree of Doctor of Philosophy, July 2019 The Morita-Baylis-Hillman reaction (MBHR) is a carbon-carbon bond forming reaction that affords multifunctional Morita-Baylis-Hillman adducts (MBHA) with various synthetic applications. Unfortunately, many of the synthetic applications of these adducts cannot be realised because these adducts are formed in racemic form. This thesis has investigated functionalisation of enantiopure MBHA obtained using biocatalytic methods. The first part of the thesis describes the use of enantiopure aldehydes N-Boc-L-phenylalaninal and N-Boc-D-phenylalaninal to synthesize several Morita-Baylis-Hillman adducts in order to obtain diastereomers that would be separable by chromatographic methods. Unfortunately, this approach proved unsuccessful due to racemization of the aldehydes or MBHA under the reaction conditions applied. The second approach described is the resolution of racemic MBH acetates and esters using different enzymes. This exercise led to the identification of several lipases that were able to resolve racemic MBH acetates with excellent enantiomeric excess (ee) values and enantiomeric ratios (E). Racemic MBH adducts derived from the reaction of acrylonitrile with benzaldehyde, cinnamaldehyde and hydrocinnamaldehyde were successfully resolved. In each case the (+)-alcohol products were isolated in 94 - 97% ee after lipase-mediated enzymatic kinetic resolution of the corresponding acetates. Mosher’s ester derivatisation protocol was used to determine the absolute configuration of the resolved adducts, which was found to be (S). A lipase from Pseudomonas fluorescens, and Candida antarctica type B were found to be the best-performing enzymes. The last part of the thesis investigated the use of nitrogen nucleophiles for Michael addition to MBH adducts. The process confirmed that the use of nitrogen nucleophiles on TBS protected MBH adducts afforded ...
format Thesis
author Juma, Wanyama Peter
author_facet Juma, Wanyama Peter
author_sort Juma, Wanyama Peter
title An investigation of the enzymatic kinetic resolution of Morita-Baylis-Hillman adducts and their further functionalisation
title_short An investigation of the enzymatic kinetic resolution of Morita-Baylis-Hillman adducts and their further functionalisation
title_full An investigation of the enzymatic kinetic resolution of Morita-Baylis-Hillman adducts and their further functionalisation
title_fullStr An investigation of the enzymatic kinetic resolution of Morita-Baylis-Hillman adducts and their further functionalisation
title_full_unstemmed An investigation of the enzymatic kinetic resolution of Morita-Baylis-Hillman adducts and their further functionalisation
title_sort investigation of the enzymatic kinetic resolution of morita-baylis-hillman adducts and their further functionalisation
publishDate 2019
url https://hdl.handle.net/10539/29573
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_relation Juma, Peter Wanyama, (2019) An investigation of the enzymatic kinetic resolution of Morita-Baylis-Hillman adducts and their further functionalisation, University of the Witwatersrand, Johannesburg, https://hdl.handle.net/10539/29573
https://hdl.handle.net/10539/29573
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