Bowen Lei, Xiaojiao Wang, Lifang Ma, Huixuan Jiao, Lisi Zhu and Ziyuan Li
Org. Biomol. Chem., 2017,15, 6084-6088
DOI:
10.1039/C7OB01083D,
Communication
A novel and concise C5-alkylation of oxazoles using alkylboronic acids as alkyl donors via Pd(II)-catalysed C–H bond activation has been achieved in moderate to good yields with satisfactory functional group tolerance. Instead of commonly used BQ as a key promoter, DDQ was discovered to be a better additive that significantly promoted this alkylation. This efficient and advanced method represents the first C(sp2)–C(sp3) cross-coupling reaction at the C5-position of oxazoles, which is particularly attractive due to its potential applications in the late-stage functionalization of oxazole-containing bioactive molecules.