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An approach to the intramolecular Diels–Alder reaction has led to a cascade synthesis of complex carbocycles composed of three fused rings and up to five stereocenters with complete stereocontrol. Computational analysis reveals that the reaction proceeds by a Michael/Michael/cyclopropanation/epimerization cascade in which size and coordination of the counterion is key. This date set contains DFT optimised structures as described in the title paper.
cyclopropanes, stereoselectivity, DFT, computational chemistry, diels-alder
cyclopropanes, stereoselectivity, DFT, computational chemistry, diels-alder
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