Synlett 2014; 25(12): 1713-1716
DOI: 10.1055/s-0034-1378276
letter
© Georg Thieme Verlag Stuttgart · New York

Decarboxylative Knoevenagel-Type Reactions on Tetronamides: Synthesis of 5-Ylidene-4-Amino-2(5H)-Furanones

Alexandre Ear
a   Sorbonne Universités. UPMC Univ Paris 06, UMR CNRS 8232, Institut Parisien de Chimie Moléculaire, 75005 Paris, France   Email: luc.dechoux@upmc.fr
b   CNRS UMR 8232, Institut Parisien de Chimie Moléculaire, 75005 Paris, France
,
Valérie Toum
a   Sorbonne Universités. UPMC Univ Paris 06, UMR CNRS 8232, Institut Parisien de Chimie Moléculaire, 75005 Paris, France   Email: luc.dechoux@upmc.fr
b   CNRS UMR 8232, Institut Parisien de Chimie Moléculaire, 75005 Paris, France
,
Serge Thorimbert
a   Sorbonne Universités. UPMC Univ Paris 06, UMR CNRS 8232, Institut Parisien de Chimie Moléculaire, 75005 Paris, France   Email: luc.dechoux@upmc.fr
b   CNRS UMR 8232, Institut Parisien de Chimie Moléculaire, 75005 Paris, France
,
Luc Dechoux*
a   Sorbonne Universités. UPMC Univ Paris 06, UMR CNRS 8232, Institut Parisien de Chimie Moléculaire, 75005 Paris, France   Email: luc.dechoux@upmc.fr
b   CNRS UMR 8232, Institut Parisien de Chimie Moléculaire, 75005 Paris, France
› Author Affiliations
Further Information

Publication History

Received: 11 April 2014

Accepted after revision: 11 May 2014

Publication Date:
06 June 2014 (online)


Abstract

A detailed account regarding the synthesis of 5-ylidene-2(5H)-furanones is given. The key step is a decarboxylative ­Knoevenagel-type reaction of tetronamides with various α-functionalized aldehydes. The synthesis of protected basidalin is presented.

 
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