Merging nucleophilic phosphine catalysis and photocatalysis for the rapid assembly of 2-oxabicyclo-[2.1.1]hexane scaffolds from feedstock allyl alcohols.
| Autor: | Whalley DM; Medicinal Chemistry, Research and Early Development, Oncology R&D AstraZeneca Cambridge CB2 0AA UK david.whalley2@astrazeneca.com olivier.lorthioir@astrazeneca.com., Carlino L; Medicinal Chemistry, Research and Early Development, Oncology R&D AstraZeneca Cambridge CB2 0AA UK david.whalley2@astrazeneca.com olivier.lorthioir@astrazeneca.com., Putra OD; Early Product Development and Manufacturing, Pharmaceutical Sciences R&D AstraZeneca Pepparedsleden 1, Mölndal SE-43183 Gothenburg Sweden., Anderson NA; Medicinal Chemistry, Research and Early Development, Oncology R&D AstraZeneca Cambridge CB2 0AA UK david.whalley2@astrazeneca.com olivier.lorthioir@astrazeneca.com., Coote SC; Department of Chemistry, University of Bath 1 South, Claverton Down Bath BA2 7AY UK., Lorthioir O; Medicinal Chemistry, Research and Early Development, Oncology R&D AstraZeneca Cambridge CB2 0AA UK david.whalley2@astrazeneca.com olivier.lorthioir@astrazeneca.com. |
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| Jazyk: | angličtina |
| Zdroj: | Chemical science [Chem Sci] 2024 Nov 04; Vol. 15 (46), pp. 19564-19570. Date of Electronic Publication: 2024 Nov 04 (Print Publication: 2024). |
| DOI: | 10.1039/d4sc06684g |
| Abstrakt: | The previously unreported combination of nucleophilic phosphine catalysis and energy transfer catalysis allows for the rapid construction of structurally distinct 2-oxabicyclo[2.1.1]hexanes (2-oxa-BCH) from readily available building blocks with high atom economy. Previous multistep routes to these important phenyl ring bioisosteres have largely depended on the use of bespoke strain-release agents or on multiple post-functionalisation reactions to access structural diversity of the scaffold. In contrast, this cascade reaction allows the medicinal chemist to exploit the breadth of commercial allyl alcohols to synthesise systematically diverse 2-oxa-BCH architectures. Using a combination of polar and radical disconnections in the same reaction flask, every position of the scaffold can be substituted with useful functional handles such as protected amines, esters and alcohols, as well as arenes and alkyl groups. Cyclic allyl alcohols can even be employed to yield single diastereomers of sp 3 -rich bridged spirocyclic structures. Aromatic groups at the 1-position can be varied to incorporate a plethora of arenes including medicinally relevant heterocycles such as indole, pyrazole and pyridine. Competing Interests: There are no conflicts to declare. (This journal is © The Royal Society of Chemistry.) |
| Databáze: | MEDLINE |
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