化学
废止
卡宾
配体(生物化学)
组合化学
串联
催化作用
分子内力
烯烃纤维
立体化学
迁移插入
赫克反应
对映选择合成
级联反应
还原消去
级联
作者
Zhou Luo,Yihao Zhang,Chao Zhang,Kewei Dong,Pranab K. Pramanick,Shen Zhao,Yuanyuan Liu,Yi Li
摘要
Pd-catalyzed asymmetric annulation via metal carbene is highly desired for efficient access to chiral cyclic compounds; however, such a strategy remains a considerable challenge. In this study, we report an unprecedented Pd-catalyzed asymmetric [4 + 1] annulation through a tandem carbene migratory insertion/Heck reaction, facilitated by an asymmetric ligand relay strategy. This approach provides an efficient protocol to access enantio-enriched α-alkylidene 3-substituted indanones. A wide range of substrates could be tolerated in the catalytic system, furnishing products with good to excellent enantioselectivity. A mechanistic study has also been conducted, which offers insights into the ligand relay catalytic system. Control experiments and DFT calculations elucidated a plausible novel E1cB mechanism for the elimination step of the Heck process, well explaining the generation of the olefin product of the Heck reaction bearing an unusual configuration. The enantio-determining step is revealed by DFT calculations to be a concerted process involving carbene formation and migratory insertion.
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