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The ( Z )‐β‐thioenamides is a valuable motif in many drugs. However, it's stereoselective synthesis is still facing challenge. Herein, we firstly reported a general and efficient approach for highly stereoselective synthesis of them by using ( Z )‐enamide‐iodines with thiols under transition metal‐free conditions.
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Kang et al. (2024) studied this question.
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