Synthesis 2015; 47(02): 209-215
DOI: 10.1055/s-0034-1379142
paper
© Georg Thieme Verlag Stuttgart · New York

Metal-Free, One-Pot Synthesis of Allylic and Benzylic Esters via Decarboxylation and C–H Bond Activation

Authors

  • Hanjie Mo

    a   School of Pharmaceutical and Chemical Engineering, Taizhou University, Taizhou 317000, P. R. of China
  • Dingben Chen

    a   School of Pharmaceutical and Chemical Engineering, Taizhou University, Taizhou 317000, P. R. of China
  • Lingzhen Xu

    a   School of Pharmaceutical and Chemical Engineering, Taizhou University, Taizhou 317000, P. R. of China
    b   College of Chemical Engineering and Materials Science, Zhejiang University of Technology, Hangzhou 310014, P. R. of China   Fax: +86(576)88660351   Email: yjg@tzc.edu.cn
  • Di Chen

    a   School of Pharmaceutical and Chemical Engineering, Taizhou University, Taizhou 317000, P. R. of China
  • Fuyou Pan

    a   School of Pharmaceutical and Chemical Engineering, Taizhou University, Taizhou 317000, P. R. of China
  • Jianguo Yang*

    a   School of Pharmaceutical and Chemical Engineering, Taizhou University, Taizhou 317000, P. R. of China
Further Information

Publication History

Received: 16 June 2014

Accepted after revision: 18 August 2014

Publication Date:
02 October 2014 (online)


Graphical Abstract

Preview

Abstract

A tetrabutylammonium iodide catalyzed method has been developed for the one-pot synthesis of allylic and benzylic esters from α-oxo carboxylic acids and alkenes/alkylbenzenes via decarboxylation and C–H bond activation. Various allylic and benzylic esters were obtained in good yield.

Supporting Information