Advances in the 1,2-Metalate Rearrangement Chemistry of Alkenylboronates

Abstract Synthetic methods that involve the formation of multiple bonds in a one-pot fashion have played a crucial role in organic chemistry. However, many features of these approaches are still limited, such as stereocontrol and chemoselectivity, especially when nonadjacent stereocenters are formed. Herein, we outlined our efforts in addressing these challenges by advancing the 1,2-metalate shift of alkenylboronic esters. 1 Introduction 2 1,2-Migration Strategy on Nitrogen-Containing Heterocyclic Substrates 3 Enantioselective Allylation with Metal(π-Allyl) Intermediates 4 Conclusion

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Publication Details

Journal
Synlett
Published
2025-02-04
DOI
https://doi.org/10.1055/a-2532-4989
Citations
3
Primary Topic
Chemical Synthesis and Reactions
Type
article
Field-Weighted Citation Impact
2.81

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article

Advances in the 1,2-Metalate Rearrangement Chemistry of Alkenylboronates

Khoa Tran, Joseph M. Ready
3 citations
Synlett
Chemical Synthesis and Reactions
2.81
article

Advances in the 1,2-Metalate Rearrangement Chemistry of Alkenylboronates

Khoa Tran, Joseph M. Ready
article en
3 citations

Abstract

Abstract Synthetic methods that involve the formation of multiple bonds in a one-pot fashion have played a crucial role in organic chemistry. However, many features of these approaches are still limited, such as stereocontrol and chemoselectivity, especially when nonadjacent stereocenters are formed. Herein, we outlined our efforts in addressing these challenges by advancing the 1,2-metalate shift of alkenylboronic esters. 1 Introduction 2 1,2-Migration Strategy on Nitrogen-Containing Heterocyclic Substrates 3 Enantioselective Allylation with Metal(π-Allyl) Intermediates 4 Conclusion

SynlettVol. 36(10)
Southwestern Medical Center (US), Southwestern Medical Center (US), The University of Texas Southwestern Medical Center (US)
Welch Foundation
Openalex Percentile: Top 12%
Chemical Synthesis and Reactions
2.81
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