1,2‐Boronate Rearrangement: An Efficient Tool for the Opening, Functionalization and Formation of Strained Cycles
Abstract: The 1,2‐metallate rearrangement occurring with boronate complexes is a strategy of choice for the synthesis of organoboron compounds, giving a direct access to highly functionalized molecules. Lately, significant progress has been made in the use of this reaction for the opening, the functionalization, and the formation of strained cycles. In this review, we will highlight these recent advances, focusing on cycloalkanes and oxygen‐ or nitrogen‐containing strained cycles.
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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1,2‐Boronate Rearrangement: An Efficient Tool for the Opening, Functionalization and Formation of Strained Cycles ; volume:2022 ; number:41 ; year:2022 ; extent:17
European journal of organic chemistry ; 2022, Heft 41 (2022) (gesamt 17)
- Creator
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Blieck, Rémi
de la Torre, Aurélien
- DOI
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10.1002/ejoc.202200920
- URN
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urn:nbn:de:101:1-2022110314073769904323
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:27 AM CEST
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Associated
- Blieck, Rémi
- de la Torre, Aurélien
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