Abstract
Quantitative analysis of the transition state (TS) structures for the reactions between 5-Cl- or 5-SiMe 3-2-adamantyl cations and methanol revealed that the magnitude of antiperiplanar hyperconjugative stabilization involving the incipient bond (the AP effect) decrease at TS, strongly suggesting that the AP effect contributes to `net destabilization' of TS (i.e., increase in activation energy), in sharp contrast to the proposals of the Felkin–Anh and the Cieplak models. The equilibrium population between two bridge(C1–C2–C3)-flipping E– Z cation conformers was found to be the origin of facial diastereoselection of these carbocations.
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