Author:
Gkizis Petros L.,Serviou Stamatis K.,Balaskas Angelos,Kokotos Christoforos G.,Constantinou Constantinos T.,Triandafillidi Ierasia
Abstract
AbstractThe phenol moiety appears in a wide variety of natural products, exhibiting biological activity, and in numerous active pharmaceutical compounds. Boronic acids are potential precursors of the phenol scaffold, and a plethora of efforts has been focused in developing novel and green protocols, targeting their chemoselective transformation into phenols. Photochemistry is a rapidly expanding research field converting light energy into chemical potential. Photochemical aerobic processes possess additional advantages to photochemistry and may find applications in chemical industries. Herein, a low-catalyst-loading anthraquinone-catalyzed photochemical process is demonstrated, under CFL lamp irradiation, while exploiting 2-Me-THF as the reaction medium for the conversion of boronic acids into phenols. Furthermore, a broad substrate scope was employed.
Funder
Hellenic Foundation for Research and Innovation
Cited by
4 articles.
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