Substituted quinoxalines are known building blocks for compounds with pharmacological, agricultural, and material uses. Forming carbon-heteroatom bonds at the 2,3-positions on quinoxaline can be challenging. 2,3-chloroquinoxaline can undergo nucleophilic aromatic substitution however it must be in the presence of metal catalysts. A range of nucleophiles are investigated to showcase the broad range of potential substitution partners that can be incorporated effectively into the 2,3-disubstituted scaffold. This research focuses on a robust microwave-assisted one-pot procedure to gain efficient access to symmetrically 2,3-substituted quinoxalines without the use of a metal catalyst.
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Univ Novi Sad, Fac Sci, Dept Chem Biochem & Environm Protect, Trg Dositeja Obradovica 3, Novi Sad 21000, SerbiaUniv Novi Sad, Fac Sci, Dept Chem Biochem & Environm Protect, Trg Dositeja Obradovica 3, Novi Sad 21000, Serbia
Grbovic, Ljubica M.
Pavlovic, Ksenija J.
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Univ Novi Sad, Fac Sci, Dept Chem Biochem & Environm Protect, Trg Dositeja Obradovica 3, Novi Sad 21000, SerbiaUniv Novi Sad, Fac Sci, Dept Chem Biochem & Environm Protect, Trg Dositeja Obradovica 3, Novi Sad 21000, Serbia
Pavlovic, Ksenija J.
Jovanovic-Santa, Suzana S.
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Univ Novi Sad, Fac Sci, Dept Chem Biochem & Environm Protect, Trg Dositeja Obradovica 3, Novi Sad 21000, SerbiaUniv Novi Sad, Fac Sci, Dept Chem Biochem & Environm Protect, Trg Dositeja Obradovica 3, Novi Sad 21000, Serbia
Jovanovic-Santa, Suzana S.
Vasiljevic, Bojana R.
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Univ Novi Sad, Fac Sci, Dept Chem Biochem & Environm Protect, Trg Dositeja Obradovica 3, Novi Sad 21000, SerbiaUniv Novi Sad, Fac Sci, Dept Chem Biochem & Environm Protect, Trg Dositeja Obradovica 3, Novi Sad 21000, Serbia