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 Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, FranceUniv Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, France
Rosales-Hurtado, Miyanou
Duvauchelle, Valentin
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Univ Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, FranceUniv Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, France
Duvauchelle, Valentin
Benimelis, David
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Univ Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, FranceUniv Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, France
Benimelis, David
Ogawa-Okada, Maya
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Western Univ Hlth Sci, Dept Basic Med Sci, Coll Osteopath Med Pacific, Pomona, CA USA
Just Evotec Biol, Redmond, WA USAUniv Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, France
Ogawa-Okada, Maya
Yamamoto, Naofumi
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Western Univ Hlth Sci, Dept Basic Med Sci, Coll Osteopath Med Pacific, Pomona, CA USAUniv Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, France
Yamamoto, Naofumi
Meffre, Patrick
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Univ Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, FranceUniv Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, France
Meffre, Patrick
Szurmant, Hendrik
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Western Univ Hlth Sci, Dept Basic Med Sci, Coll Osteopath Med Pacific, Pomona, CA USAUniv Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, France
Szurmant, Hendrik
Benfodda, Zohra
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Univ Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, FranceUniv Nimes, UPR CHROME, Rue Dr G Salan, F-30021 Nimes 1, France
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Indian Inst Chem Technol, Organ Chem Div 1, Hyderabad 500607, Andhra Pradesh, IndiaIndian Inst Chem Technol, Organ Chem Div 1, Hyderabad 500607, Andhra Pradesh, India
Nageswar, Y. V. D.
Reddy, K. Harsha Vardhan
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Indian Inst Chem Technol, Organ Chem Div 1, Hyderabad 500607, Andhra Pradesh, IndiaIndian Inst Chem Technol, Organ Chem Div 1, Hyderabad 500607, Andhra Pradesh, India
Reddy, K. Harsha Vardhan
Ramesh, K.
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Indian Inst Chem Technol, Organ Chem Div 1, Hyderabad 500607, Andhra Pradesh, IndiaIndian Inst Chem Technol, Organ Chem Div 1, Hyderabad 500607, Andhra Pradesh, India
Ramesh, K.
Murthy, S. Narayana
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Indian Inst Chem Technol, Organ Chem Div 1, Hyderabad 500607, Andhra Pradesh, IndiaIndian Inst Chem Technol, Organ Chem Div 1, Hyderabad 500607, Andhra Pradesh, India
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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