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Updated: Aug 15, 2026

Facile Preparation of (2Z,4E)-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
Enantioselective carboamination of olefins catalyzed by transition metals
Zhi-Kun Zhang1, Velayudham Sankar1, Haichao Shen1
1State Key Laboratory of Green Chemical Synthesis and Conversion, Department of Chemistry, Fudan University, 2005 Songhu Road, Shanghai, 200438, China. yangjf@fudan.edu.cn.
Abstract:
Enantioselective olefin carboamination is the simultaneous formation of C-N and C-C bonds across an alkene. This method represents a powerful strategy to build molecular complexity with up to two vicinal stereocenters in a single operation. Over the past two decades, transition metal catalyzed enantioselective olefin carboamination has been well-developed. Various elegant studies have employed this strategy to synthesise a series of amines or aza-heterocycles with stereocenters. Initially, reactions catalyzed by noble metals such as Pd and Rh were explored, followed by the development of enantioselective carboamination reactions using non-noble metals (Fe, Co, Ni, and Cu). In this review, we will discuss enantioselective olefin carboamination catalyzed by different transition metals and provide a detailed overview of the mechanisms involved.
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