Issue 40, 2014

Direct β-acylation of 2-arylidene-1,3-indandiones with acyl chlorides catalyzed by organophosphanes

Abstract

We have developed an organophosphane-catalyzed direct β-acylation of a series of conjugated systems bearing ketone, amide and ester functionalities using acyl chlorides as trapping reagents. A wide variety of highly functional ketone derivatives were generated efficiently under very mild conditions with high yields according to our protocol. Our adducts can even be utilized as important building blocks for the synthesis of functional tri/tetracyclic pyridazine derivatives.

Graphical abstract: Direct β-acylation of 2-arylidene-1,3-indandiones with acyl chlorides catalyzed by organophosphanes

Supplementary files

Article information

Article type
Communication
Submitted
10 Jul 2013
Accepted
30 Jul 2013
First published
31 Jul 2013

Chem. Commun., 2014,50, 5304-5306

Direct β-acylation of 2-arylidene-1,3-indandiones with acyl chlorides catalyzed by organophosphanes

C. Lee, C. Sheu, C. Tsai, Z. Wu and W. Lin, Chem. Commun., 2014, 50, 5304 DOI: 10.1039/C3CC45201H

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