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Alkynones represent one class of interesting building block which are frequently founded in a variety of biologically active compounds.[1] They have been emerged as key intermediates in the synthesis of various natural products and heterocycles.[2] Therefore, a considerable interest has been attracted and numerous strategies have been explored for the synthesis of alkynones. The traditional methods mainly rely on the reactions of acid chlorides with terminal alkynes.>[3–4] However, some drawbacks remain existing, including high reaction temperature, unstable acid chlorides, and poor functional group tolerance. [ABSTRACT FROM AUTHOR]

Transition metal-catalyzed carbonylation functionalization reaction of alkenes is an attractive research area in modern organic chemistry. However, there have been very few reports on silver-catalyzed reactions in carbonylation reactions. Herein we developed a silver-catalyzed carbamoylation and carbonylative cyclization of alkenes with oxamic acids to obtain 2-acetylamino-1-tetralone derivatives. Various desired cyclized products were formed in moderate to good yields through radical intermediates., (© 2024 Wiley‐VCH GmbH.)