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 |
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