Abstract
A variety of flavones were expediently synthesized from readily accessible chromanones via a one-pot sequence involving Pd(ii)-catalyzed dehydrogenation and oxidative boron-Heck coupling with arylboronic acid pinacol esters. In particular, the use of arylboronic acid pinacol esters was found to significantly improve the yield of the reaction.
Original language | English |
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Pages (from-to) | 777-784 |
Number of pages | 8 |
Journal | Organic and Biomolecular Chemistry |
Volume | 14 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2016 |
Bibliographical note
Publisher Copyright:© 2016 The Royal Society of Chemistry.