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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.

Authors

P.R. Parry

B. Tarbit



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
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 1
Issue 9
Pages 1447-1449