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These actions are very important for the viability regarding the procedure where development of just one stereoisomer is necessary. The results suggest that the inclusion effect is under thermodynamic and not kinetic control and therefore the key aspect determining the reaction stereoselectivity would be the stereochemical limitations enforced by all substituents within the cyclohexane ring. The DFT results indicate that cyclohexylthiol should behave similarly to p-toluylthiol, the main
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