Denitrative cross-couplings of nitrostyrenes

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Abstract

Interestingly, β-nitrostyrenes, typically bench stable compounds, are highly promising cross-coupling partners, due to their excellent availability and well understood reactivity. In this review, we report on the discovery and advancements, in the field of stereoselective, denitrative cross-couplings of β-nitrostyrenes with miscellaneous organic reagents. The rapidly expanding field offers alternative access to a broad range of functionalized alkenes, including β-alkylated styrenes, chalcones, stilbenes, cinnamic acids, and conjugated sulfones and phosphonates. The most important mechanistic pathways are briefly discussed, to familiarize readers with the elementary reactions occurring during the coupling.

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Marčeková, M., Ferko, B., Detková, K. R., & Jakubec, P. (2020, August 1). Denitrative cross-couplings of nitrostyrenes. Molecules. MDPI AG. https://doi.org/10.3390/molecules25153390

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