P.R. Parry
5-Formyl-2-furylboronic acid as a versatile bifunctional reagent for the synthesis of pi-extended heteroarylfuran systems
Parry, P.R.; Bryce, M.R.; Tarbit, B.
Abstract
5-Formyl-2-furylboronic acid reacts cleanly with a range of heteroaryl bromides under Suzuki-Miyaura cross-coupling conditions to produce 2-formyl-5-heteroarylfuran derivatives. Subsequent Wittig olefination reactions afford pi-conjugated alkene-pyridyl-furan derivatives.
Citation
Parry, P., Bryce, M., & Tarbit, B. (2003). 5-Formyl-2-furylboronic acid as a versatile bifunctional reagent for the synthesis of pi-extended heteroarylfuran systems. Organic and Biomolecular Chemistry, 1(9), 1447-1449
| Journal Article Type | Article |
|---|---|
| Publication Date | 2003-05 |
| Journal | Organic and Biomolecular Chemistry |
| Print ISSN | 1477-0520 |
| Electronic ISSN | 1477-0539 |
| Publisher | Royal Society of Chemistry |
| Peer Reviewed | Peer Reviewed |
| Volume | 1 |
| Issue | 9 |
| Pages | 1447-1449 |
| Public URL | https://durham-repository.worktribe.com/output/1601197 |
You might also like
Downloadable Citations
About Durham Research Online (DRO)
Administrator e-mail: dro.admin@durham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search