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Stereoretention in Styrene Heterodimerisation Promoted by One-Electron Oxidants

revised on 05.05.2020, 16:29 and posted on 06.05.2020, 08:55 by Xinglong Zhang, Robert Paton

Radical cations generated from the oxidation of C=C p-bonds are synthetically useful reactive intermediates for C–C and C–X bond formation. Radical cation formation, induced by sub-stoichiometric amounts of external oxidant, are important intermediates in the Woodward-Hoffmann thermally disallowed [2+2] cycloaddition of electron-rich alkenes. Using density functional theory (DFT), we report the detailed mechanisms underlying the intermolecular heterodimerisation of anethole and β-methylstyrene to give unsymmetrical, tetra-substituted cyclobutanes. Reactions between trans-alkenes favour the all-trans adduct, resulting from a kinetic preference for anti-addition reinforced by reversibility at ambient temperatures since this is also the thermodynamic product; on the other hand, reactions between a trans-alkene and a cis-alkene favour syn-addition, while exocyclic rotation in the acyclic radical cation intermediate is also possible since C-C forming barriers are higher. Computations are consistent with the experimental observation that hexafluoroisopropanol (HFIP) is a better solvent than acetonitrile, in part due to its ability to stabilize the reduced form of the hypervalent iodine initiator by hydrogen bonding, but also through the stabilisation of radical cationic intermediates along the reaction coordinate.


Agency for Science, Technology and Research (A*STAR), Singapore

EPSRC Centre for Doctoral Training in Theory and Modelling in Chemical Sciences (EP/L015722/1)

National Science Foundation (ACI-1532235 and ACI-1532236)

Extreme Science and Engineering Discovery Environment (XSEDE) allocation TG-CHE180056


Email Address of Submitting Author


University of Oxford


United Kingdom

ORCID For Submitting Author


Declaration of Conflict of Interest

No conflicts of Interest

Version Notes

This is the initial submission (v1).