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Organic Chemistry Forum / Re: Regioselectivity in Se-Reactions in the context of polycyclic compounds
« Last post by Venoxis on Yesterday at 11:38:25 PM »Thank you for your reply Borek. I think it might be a combination of electron distribution (nucleophilic/electrophilic potential of individual C positions), the amount of steric hindrance and the type of reaction applied that determines where the next reaction takes place. Let's see what an organic chemist will say about this.
Z ukłonami, (hope that was correct)
Venoxis
Z ukłonami, (hope that was correct)
Venoxis