Copper‐Catalyzed Borylation of Cyclic Sulfamidates: Access to Enantiomerically Pure (β‐and γ‐Amino­alkyl)boronic Esters

Cyclic sulfamidates undergo borylation under copper‐catalyzed conditions using B(2)pin(2) to give enantiomerically (and diasteromerically) defined (aminoalkyl)boronic esters. External iodide is essential, but the intermediacy of simple alkyl iodides has been excluded; N‐sulfated intermediates are ke...

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Detalles Bibliográficos
Autores principales: Ursinyova, Nina, Bedford, Robin B., Gallagher, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY‐VCH Verlag 2015
Materias:
Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770434/
http://dx.doi.org/10.1002/ejoc.201501492

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770434/
http://dx.doi.org/10.1002/ejoc.201501492

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