Title of article
Bronsted acid catalyzed direct oxidative arylation of 1,4-naphthoquinone
Author/Authors
Kap?on، Katarzyna نويسنده Department of Organic Chemistry, Maria Curie-Sk?odowska University, 33 - Gliniana Street, 20-614 Lublin, Poland , , Demchuk، Oleg M. نويسنده Department of Organic Chemistry, Maria Curie-Sk?odowska University, 33 - Gliniana Street, 20-614 Lublin, Poland , , Wieczorek، Marta نويسنده Department of Organic Chemistry, Maria Curie-Sk?odowska University, 33 - Gliniana Street, 20-614 Lublin, Poland , , Pietrusiewicz، K. Micha? نويسنده Department of Organic Chemistry, Maria Curie-Sk?odowska University, 33 - Gliniana Street, 20-614 Lublin, Poland ,
Issue Information
فصلنامه با شماره پیاپی 9 سال 2014
Pages
14
From page
23
To page
36
Abstract
An inexpensive straightforward approach to direct oxidative twofold C-H arylation of 1,4-naphthoquinone catalyzed by readily available Br?nsted acids was developed. Under the simple and easily achievable reaction conditions, electron-rich aromatics undergo Friedel-Crafts type functionalization to furnish 2-arylonaphthoquinones in good yields. The attempt to rationalize the scope and limitation of the approach based on desktop PC DFT calculation and reactivity indexes theory was taken up.
Journal title
Current Chemistry Letters
Serial Year
2014
Journal title
Current Chemistry Letters
Record number
1037980
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