Efficient Synthesis of Chromones with Alkenyl Functionalities by the Heck Reaction
Tamás Patonay A C , Attila Vasas A , Attila Kiss‐Szikszai A , Artur M. S. Silva B and José A. S. Cavaleiro B
+ Author Affiliations
- Author Affiliations
A Department of Organic Chemistry, University of Debrecen, Egyetem tér 1, H‐4032 Debrecen, Hungary.
B Department of Chemistry and Química Orgânica, Produtos Naturais e Agroalimentares, University of Aveiro, 3810‐193 Aveiro, Portugal.
C Corresponding author. Email: tpatonay@puma.unideb.hu
Australian Journal of Chemistry 63(11) 1582-1593 https://doi.org/10.1071/CH10295
Submitted: 9 August 2010 Accepted: 7 October 2010 Published: 11 November 2010
Abstract
The usefulness of the Heck reaction in the field of chromones has been demonstrated. Bromochromones with the halogen atom in their rings A and B were reacted with various terminal alkenes to give hitherto unknown alkenyl‐substituted chromones. Reactivity of the substrates was found to markedly depend on the position of the bromine atom. Under phosphine‐free conditions using a phase‐transfer catalyst additive (tetrabutylammonium bromide), shorter reaction periods and usually higher yields were obtained.
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