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

J Org Chem. 2023 Nov 17;88(22):15975-15982. doi: 10.1021/acs.joc.3c01215. Epub 2023 Oct 27.

Abstract

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.