Generation and Utility of Cyclic Dienyl Gold Carbene Intermediates

作者：Cheng Zhang, Kemiao Hong, Shanliang Dong, Mengting Liu, Matthias Rudolph, Martin C. Dietl, Jian Yin, A. Stephen K. Hashmi, Xinfang Xu · 发表于：ACS Catalysis · 年份：2023 · DOI：10.1021/acscatal.2c06188 · 被引用次数：24 · 研究领域：Catalytic Alkyne Reactions、Cyclopropane Reaction Mechanisms、Catalytic C–H Functionalization Methods

Exploration of intermediates that enable chemo- and stereoselective cycloaddition reactions for the expeditious construction of fused- and bridged-ring systems continues to draw a great deal of interest from the synthetic community. Vinylcarbene intermediates, which serve as 1- or 3-carbon building blocks, have been frequently used for the construction of cyclic frameworks through the successive formation of multiple carbon–carbon or/and carbon–heteroatom bonds. Here, we present a concise strategy for the catalytic generation of cyclic dienyl gold carbene species (Au-CDC) via a selective gold-promoted diazo-enyne carbocyclization process. Following cycloadditions of these in situ formed carbene intermediates with different types of dipolarophiles are disclosed, producing a diverse array of fused and bridged skeletons with high chemo- and stereoselectivity. This method provides a tool resulting in straightforward access to ring systems with structural complexity and diversity, and is a substantial complementary protocol to existing methods relying on using open-chained vinylcarbene species. The subsequent exploration of these generated cyclopentadiene motifs with dipolarophiles in accessing targets of polycyclic structures can further increase this rings-per-operation count, leading conceptually to the Au-CDC as a key bridge capable of connecting back-to-back cycloadditions.