1114965-84-2Relevant academic research and scientific papers
BiCl3-catalysed nucleophilic substitution of Baylis-Hillman adducts with alcohols
Li, Jian,Liu, Xiaotao,Zhao, Peichao,Jia, Xueshun
experimental part, p. 159 - 162 (2009/05/30)
An efficient nucleophilic substitution of Baylis-Hillman adducts with alcohols catalysed by 10 mol% BiCI3, affords functionalised ethers. Water was the only side product.
FeCl3-catalyzed nucleophilic substitution of Baylis-Hillman adducts with alcohols
Jia, Xueshun,Zhao, Peichao,Liu, Xiaotao,Li, Jian
, p. 1617 - 1628 (2008/09/20)
FeCl3-catalyzed nucleophilic substitution reaction of Baylis-Hillman adducts with alcohols is described. The present protocol allows for the efficient syntheses of many kinds of functional ethers. This conversion is also a green route because water is the only side product. Copyright Taylor & Francis Group, LLC.
