Pd-Catalyzed C(sp2)-H/C(sp2)-H Coupling of Limonene

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Abstract

Limonene undergoes a regioselective Pd(II)-catalyzed C(sp2)-H/C(sp2)-H coupling with acrylic acid esters and amides, α,β-unsaturated ketones, styrenes, and allyl acetate, affording novel 1,3-dienes. DFT computations gave results in accord with the experimental results and allowed for the formulation of a plausible mechanism. The postfunctionalization of one of the coupled products was achieved via a large-scale Sonogashira reaction conducted under micellar catalysis.

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Di Matteo, M., Gagliardi, A., Pradal, A., Veiros, L. F., Gallou, F., & Poli, G. (2024). Pd-Catalyzed C(sp2)-H/C(sp2)-H Coupling of Limonene. Journal of Organic Chemistry, 89(15), 10451–10461. https://doi.org/10.1021/acs.joc.4c00501

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