薗头偶联反应
化学
手性(物理)
组合化学
催化作用
共轭体系
对映选择合成
分子
立体化学
羰基化
轴手性
钯
基质(水族馆)
有机合成
纳米技术
天然产物
表面改性
计算化学
有机分子
作者
Pengyong Fang,Song‐Zhou Cai,Yuxing Wang,Dacao Yu,Haoxiang Wan,Z L Zhang,Jinguo Long,Xianjie Fang
标识
DOI:10.1021/acscatal.6c02416
摘要
Ynones are fundamental structural motifs found in a broad spectrum of bioactive molecules and pharmaceuticals. Owing to their intrinsic conjugated reactivity, centrally chiral ynones serve as versatile building blocks in organic synthesis. However, the current access to centrally chiral ynones relies predominantly on the stepwise asymmetric functionalization of pre-existing ynone derivatives. In this study, we present a palladium-catalyzed asymmetric carbonylative Sonogashira reaction of cyclopropenes, which enables the simultaneous construction of the ynone framework and the establishment of central chirality, thereby eliminating the need for post-functionalization. The protocol features mild reaction conditions, high atom economy, and a broad substrate scope. Moreover, its practical utility is demonstrated through gram-scale synthesis and diverse product derivatizations, offering a valuable perspective for the construction of centrally chiral ynones.
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