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
Authors
- Khoa Tran (ORCID: https://orcid.org/0000-0001-9270-0511)
- Joseph M. Ready (ORCID: https://orcid.org/0000-0003-1305-9581)
Institutions
- Southwestern Medical Center (US)
- Southwestern Medical Center (US)
- The University of Texas Southwestern Medical Center (US)
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
Funders
- Welch Foundation