Abstract
AbstractScandium(III) triflate promoted highly selective addition of thiols to functionalized olefins under mild conditions. The addition follows anti‐Markovnikov regioselectivities, which are unusual for Lewis acids‐catalyzed hydrothiolation. This reaction marks broad functional groups tolerance, which opens a beneficial synthetic route to functionalized and biologically active thio‐compounds. This method is broadly applicable and offers a simple work‐up in the green manner.magnified image
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