Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles
<p>This thesis describes the combination of non-stabilized nucleophiles and prochiral/racemic electrophiles in transition metal catalyzed asymmetric transformations. These enantioselective reactions have tremendous potential for the formation of chiral building blocks and new structural motifs...
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| Format: | Thesis |
| Language: | English |
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2017
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| _version_ | 1797097469371219968 |
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| author | Schäfer, P |
| author2 | Fletcher, S |
| author_facet | Fletcher, S Schäfer, P |
| author_sort | Schäfer, P |
| collection | OXFORD |
| description | <p>This thesis describes the combination of non-stabilized nucleophiles and prochiral/racemic electrophiles in transition metal catalyzed asymmetric transformations. These enantioselective reactions have tremendous potential for the formation of chiral building blocks and new structural motifs that can be found in a variety of natural products and their derivatives.</p> <p>The first part of the thesis focuses on the synthetic approach towards anti-cancer active diterpenoid structures. The two key steps involve a Cu-catalyzed asymmetric conjugate addition of alkylzirconocenes to enones and an intramolecular oxidative cyclisation. Particular investigations into the cyclisation are made with organocatalysis, transition metal catalysis and electrochemistry for the formation of these tricyclic scaffolds.</p> <p>In the second part this work builds on the Rh-catalyzed asymmetric Suzuki–Miyaura coupling of benzeneboronic acids and cyclic allyl chlorides, which has been developed in our group. Here, the main point is to use more challenging coupling partners, such as heteroaromatic boronic acids, which are coupled to racemic cyclic allyl halides. The utility of this method is demonstrated by performing further transformations and an asymmetric synthesis of the natural product (+)- isoanabasine.</p> <p>The last chapter describes the development of a new asymmetric Hiyama coupling of arylsiloxanes with racemic cyclic allyl chloride. Attempts are made to generate substrates that are not accessible via the asymmetric Suzuki–Miyaura reaction. After extensive optimisation a variety of arylsiloxanes is generated and tested with the best conditions to prove its utility in comparison to the asymmetric Suzuki–Miyaura coupling.</p> |
| first_indexed | 2024-03-07T04:55:57Z |
| format | Thesis |
| id | oxford-uuid:d69d1861-5368-495a-932d-7e1aa6bc5dfb |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T04:55:57Z |
| publishDate | 2017 |
| record_format | dspace |
| spelling | oxford-uuid:d69d1861-5368-495a-932d-7e1aa6bc5dfb2022-03-27T08:34:48ZEnantioselective synthesis of chiral building blocks with non-stabilized nucleophilesThesishttp://purl.org/coar/resource_type/c_db06uuid:d69d1861-5368-495a-932d-7e1aa6bc5dfbEnantioselective catalysisEnglishORA Deposit2017Schäfer, PFletcher, S<p>This thesis describes the combination of non-stabilized nucleophiles and prochiral/racemic electrophiles in transition metal catalyzed asymmetric transformations. These enantioselective reactions have tremendous potential for the formation of chiral building blocks and new structural motifs that can be found in a variety of natural products and their derivatives.</p> <p>The first part of the thesis focuses on the synthetic approach towards anti-cancer active diterpenoid structures. The two key steps involve a Cu-catalyzed asymmetric conjugate addition of alkylzirconocenes to enones and an intramolecular oxidative cyclisation. Particular investigations into the cyclisation are made with organocatalysis, transition metal catalysis and electrochemistry for the formation of these tricyclic scaffolds.</p> <p>In the second part this work builds on the Rh-catalyzed asymmetric Suzuki–Miyaura coupling of benzeneboronic acids and cyclic allyl chlorides, which has been developed in our group. Here, the main point is to use more challenging coupling partners, such as heteroaromatic boronic acids, which are coupled to racemic cyclic allyl halides. The utility of this method is demonstrated by performing further transformations and an asymmetric synthesis of the natural product (+)- isoanabasine.</p> <p>The last chapter describes the development of a new asymmetric Hiyama coupling of arylsiloxanes with racemic cyclic allyl chloride. Attempts are made to generate substrates that are not accessible via the asymmetric Suzuki–Miyaura reaction. After extensive optimisation a variety of arylsiloxanes is generated and tested with the best conditions to prove its utility in comparison to the asymmetric Suzuki–Miyaura coupling.</p> |
| spellingShingle | Enantioselective catalysis Schäfer, P Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles |
| title | Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles |
| title_full | Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles |
| title_fullStr | Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles |
| title_full_unstemmed | Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles |
| title_short | Enantioselective synthesis of chiral building blocks with non-stabilized nucleophiles |
| title_sort | enantioselective synthesis of chiral building blocks with non stabilized nucleophiles |
| topic | Enantioselective catalysis |
| work_keys_str_mv | AT schaferp enantioselectivesynthesisofchiralbuildingblockswithnonstabilizednucleophiles |