Cargando…

Method for Accessing Nitrogen-Containing, B-Heteroaryl-Substituted 2,1-Borazaronaphthalenes

[Image: see text] The azaborine motif provides a mimic of aromatic systems through replacement of a C=C bond with a B–N bond. In particular, 2,1-borazaronaphthalenes, accessible through robust methods of synthesis and subsequent functionalization, afford an ideal platform to use for a variety of app...

Descripción completa

Detalles Bibliográficos
Autores principales: Davies, Geraint H. M., Zhou, Zhao-Zhao, Jouffroy, Matthieu, Molander, Gary A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5224235/
https://www.ncbi.nlm.nih.gov/pubmed/27966969
http://dx.doi.org/10.1021/acs.joc.6b02574
Descripción
Sumario:[Image: see text] The azaborine motif provides a mimic of aromatic systems through replacement of a C=C bond with a B–N bond. In particular, 2,1-borazaronaphthalenes, accessible through robust methods of synthesis and subsequent functionalization, afford an ideal platform to use for a variety of applications. However, the scope of substructures for this archetype has been limited by the lack of nitrogen-containing heteroaryls that can be incorporated within them. In this study, modified reaction conditions were developed to provide access to a wider range of substructures.