We use cookies to ensure that we give you the best experience on our website. By continuing to browse this repository, you give consent for essential cookies to be used. You can read more about our Privacy and Cookie Policy.

Durham Research Online
You are in:

Exploiting C-H borylation for the multidirectional elaboration of 2-halopyridines.

Reuven, J.A. and Salih, O.A. and Sadler, S.A. and Thomas, C.L. and Steel, P.G. (2020) 'Exploiting C-H borylation for the multidirectional elaboration of 2-halopyridines.', Tetrahedron, 76 (3). p. 29723.


Regioselectively polysubstituted pyridines can be efficiently accessed from 2-halopyridines via a sequence involving C-H borylation, Suzuki-Miyaura cross-coupling and nucleophilic aromatic substitution chemistry.

Item Type:Article
Full text:(AM) Accepted Manuscript
Available under License - Creative Commons Attribution Non-commercial No Derivatives.
Download PDF
Publisher Web site:
Publisher statement:© 2019 This manuscript version is made available under the CC-BY-NC-ND 4.0 license
Date accepted:25 November 2019
Date deposited:26 November 2019
Date of first online publication:29 November 2019
Date first made open access:29 November 2020

Save or Share this output

Look up in GoogleScholar