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Updated: May 24, 2025

Facile Preparation of 2Z,4E-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
Hydrogen Bond Promoted Carbonylative Lactonization of Alkenes
Xin Qi1,2, Yuanrui Wang1,2, Xiao-Feng Wu1,2,3
1Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Abstract:
The formation of complexed molecules through intramolecular hydrogen bond to facilitate chemical reactions is an applicable strategy in organic synthesis. Among the lactones, γ-butyrolactones is a class of biologically active and important structures. In this work, a series of γ-butyrolactones were synthesised in a green and efficient manner by carbonylation of alkenes. This reaction is also applicable to the synthesis of lactones containing natural product modules. The formation of an intramolecular hydrogen bond between the pyridine group and the hydroxyl group is imperative for enhancing the nucleophilicity of the large steric alcohol, which are challenge to lactonize. The existence of intramolecular hydrogen bond was proven with the aid of FT-IR and NMR characterisation.
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