Synthesis 2014; 46(17): 2305-2311
DOI: 10.1055/s-0033-1339110
special topic
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Ethyl Arylpropiolates through Palladium-Catalyzed Cross-Coupling­ Reactions of Aryl Iodides with In Situ Generated Lithium Tetrakis(ethoxycarbonylethynyl)indates

Autoren

  • Youngchul Park

    Department of Chemistry, Kangwon National University, Chuncheon 200-701, Republic of Korea   Fax: +82(33)2595667   eMail: phlee@kangwon.ac.kr
  • Dongjin Kang

    Department of Chemistry, Kangwon National University, Chuncheon 200-701, Republic of Korea   Fax: +82(33)2595667   eMail: phlee@kangwon.ac.kr
  • Woo Hyung Jeon

    Department of Chemistry, Kangwon National University, Chuncheon 200-701, Republic of Korea   Fax: +82(33)2595667   eMail: phlee@kangwon.ac.kr
  • Taekyu Ryu

    Department of Chemistry, Kangwon National University, Chuncheon 200-701, Republic of Korea   Fax: +82(33)2595667   eMail: phlee@kangwon.ac.kr
  • Phil Ho Lee*

    Department of Chemistry, Kangwon National University, Chuncheon 200-701, Republic of Korea   Fax: +82(33)2595667   eMail: phlee@kangwon.ac.kr
Weitere Informationen

Publikationsverlauf

Received: 21. Februar 2014

Accepted after revision: 13. April 2014

Publikationsdatum:
28. Mai 2014 (online)


Graphical Abstract

Abstract

An efficient synthetic method to access ethyl arylpropiolates has been developed; it involves a palladium-catalyzed cross-coupling reaction between a wide range of aryl iodides and lithium tetrakis(ethoxycarbonylethynyl)indates (0.35 equiv) generated in situ from indium trichloride and alkynides obtained from ethyl propiolate and n-butyllithium.

Supporting Information