Issue 49, 2014

Base-catalyzed bicyclization of dialkyl glutaconates with cinnamoylacetamides: a synthetic strategy for isoquinolinedione derivatives

Abstract

We report here that polysubstituted dihydroisoquinolones and isoquinolones can be constructed by the one-pot reaction of the readily available acyclic α,β-unsaturated carbonyl precursors and dialkyl glutaconates under mild basic conditions (1–45 min for the former vs. 1–6 h for the latter) via the domino process involving [3+3] annulation/intramolecular aza-cyclization.

Graphical abstract: Base-catalyzed bicyclization of dialkyl glutaconates with cinnamoylacetamides: a synthetic strategy for isoquinolinedione derivatives

Supplementary files

Article information

Article type
Communication
Submitted
11 Sep 2013
Accepted
17 Apr 2014
First published
17 Apr 2014

Chem. Commun., 2014,50, 6458-6460

Base-catalyzed bicyclization of dialkyl glutaconates with cinnamoylacetamides: a synthetic strategy for isoquinolinedione derivatives

L. Li, Y. Zhao, H. Wang, Y. Li, X. Xu and Q. Liu, Chem. Commun., 2014, 50, 6458 DOI: 10.1039/C3CC46931J

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