Skip to main content

Research Repository

Advanced Search

Exploiting C-H Borylation for the Multidirectional Elaboration of 2-Halopyridines

Reuven, J.A.; Salih, O.A.; Sadler, S.A.; Thomas, C.L.; Steel, P.G.

Exploiting C-H Borylation for the Multidirectional Elaboration of 2-Halopyridines Thumbnail


Authors

J.A. Reuven

O.A. Salih

S.A. Sadler

C.L. Thomas



Abstract

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.

Citation

Reuven, J., Salih, O., Sadler, S., Thomas, C., & Steel, P. (2020). Exploiting C-H Borylation for the Multidirectional Elaboration of 2-Halopyridines. Tetrahedron, 76(3), Article 130836. https://doi.org/10.1016/j.tet.2019.130836

Journal Article Type Article
Acceptance Date Nov 25, 2019
Online Publication Date Nov 29, 2019
Publication Date Jan 17, 2020
Deposit Date Nov 26, 2019
Publicly Available Date Mar 29, 2024
Journal Tetrahedron
Print ISSN 0040-4020
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 76
Issue 3
Article Number 130836
DOI https://doi.org/10.1016/j.tet.2019.130836

Files





You might also like



Downloadable Citations