Cargando…
Stereodivergent Olefination of Enantioenriched Boronic Esters
A stereodivergent coupling reaction between vinyl halides and boronic esters is described. This coupling process proceeds without a transition‐metal catalyst, instead proceeding by electrophilic selenation or iodination of a vinyl boronate complex followed by stereospecific syn or anti elimination....
Autores principales: | Armstrong, Roly J., García‐Ruiz, Cristina, Myers, Eddie L., Aggarwal, Varinder K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347846/ https://www.ncbi.nlm.nih.gov/pubmed/27958668 http://dx.doi.org/10.1002/anie.201610387 |
Ejemplares similares
-
Visible‐Light‐Mediated Decarboxylative Radical Additions to Vinyl Boronic Esters: Rapid Access to γ‐Amino Boronic Esters
por: Noble, Adam, et al.
Publicado: (2018) -
Regio‐ and Stereoselective Homologation of 1,2‐Bis(Boronic Esters): Stereocontrolled Synthesis of 1,3‐Diols and Sch 725674
por: Fawcett, Alexander, et al.
Publicado: (2016) -
50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling
por: Armstrong, Roly J., et al.
Publicado: (2017) -
Enantiospecific Alkynylation of Alkylboronic Esters
por: Wang, Yahui, et al.
Publicado: (2016) -
Desymmetrization of C
(2)‐Symmetric Bis(Boronic Esters) by Zweifel Olefinations
por: Linne, Yannick, et al.
Publicado: (2020)