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DOI: 10.1055/a-2257-7304
Unveiling Novel Synthetic Pathways through Brook Rearrangement
We gratefully acknowledge the Neubauer Family Foundation, the Council of Higher Education of Israel (MAOF fellowship), and the Hebrew University of Jerusalem for generous financial support.
Dedicated to Professor Amos B Smith, III
Abstract
The Brook rearrangement is a valuable synthetic tool that facilitates the controlled construction of complex molecules. Conventionally, it generates carbanion intermediates utilized in subsequent functionalization reactions. In this review, we will explore recent advancements in the Brook rearrangement that extend beyond the traditional functionalization reactions. Specifically, we will highlight its involvement in unusual bond cleavage, annulation reactions, and dearomatization efforts. The novelty of this rearrangement is underscored by showcasing its most recent applications.
1 Introduction
2 Novel Synthetic Pathways Involving the Brook Rearrangement
2.1 C–C and C–X Bond Formation
2.2 C–C and C–X Bond Cleavage
2.3 Stereodefined Substituted Silyl Enol and Allenol Ethers
2.4 Annulation Reactions
2.5 Dearomatization
3 Synthetic Applications
4 Conclusion
Key words
Brook rearrangement - anion relay chemistry - silyl migration - synthetic methods - complex moleculesPublikationsverlauf
Eingereicht: 16. Januar 2024
Angenommen nach Revision: 30. Januar 2024
Accepted Manuscript online:
30. Januar 2024
Artikel online veröffentlicht:
19. Februar 2024
© 2024. Thieme. All rights reserved
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For additional studies, see:
For selected studies on 1,3-C(sp2)–O silyl migration, see:
For selected studies on 1,4-C(sp2)–O silyl migration of aryl organosilicon compounds, see:
For selected studies on 1,4-C(sp2)–O silyl migration of vinyl organosilicon compounds, see:
For additional examples on sp3-type Brook rearrangement/ functionalization reaction, see:
For other carbanion-stabilizing substituents, see:
For selected studies, see:
For selected studies, see:
For selected studies, see:
For selected reviews:
For selected studies: