Abstract
AbstractDurch Behandlung des Mercapto‐azetidinons (I) mit einem 20:3‐Gemisch von Methanol und Essigsäure und gleichzeitige Reduktion mit Natriumcyanoborhydrid bei 25°C erhält man über den Thioaldehyd (II) das Dipeptid (III), das mit Iod in Tetrahydrofuran zum entsprechenden Disulfid oxidiert werden kann.
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