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Gold Catalyzed 7- endo -dig Hydroaminations Yielding 1,4-Diazepineones.

Matthew R NelliRachel L CantrellRyan E Looper
Published in: The Journal of organic chemistry (2023)
Strategies to access the 1,4-diazepindiones heterocyclic core of the TAN-1057 family of natural products revealed a successful gold-catalyzed hydroamination of yneamide tethered amines. The precursor amino-yneamides are derived from easily accessible 1,2-diamines and alkynoic acids and are efficiently cyclized to the corresponding diazepineones.
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