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A plausible explanation for the fact that tetracycle 11 is formed preferably under apolar conditions is that the tricycloundecenyl cation is only poorly solvated and therefore more reactive and less selective.
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A plausible explanation for the fact that tetracycle 11 is formed preferably under apolar conditions is that the tricycloundecenyl cation is only poorly solvated and therefore more reactive and less selective.
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For the purpose of clarity, other less relevant conformers with similar chemistry are not discussed here, see Supporting Information
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For the purpose of clarity, other less relevant conformers with similar chemistry are not discussed here, see Supporting Information.
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The same interaction exists with C(6)-H as acceptor because of the symmetry of the structure.
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The same interaction exists with C(6)-H as acceptor because of the symmetry of the structure.
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