We developed a copper-catalyzed tandem reaction of 2-aminobenzamides with tertiary amines for the formation of quinazolinone derivatives. The strategy includes two steps (cyclization and coupling) performed in one pot. A number of substrates reacted well under standard conditions to give the corresponding quinazolinone derivatives in moderate to good yields.
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Ecole Natl Super Chim Montpellier, CNRS, Inst Charles Gerhardt, UMR 5253,AM2N, F-34296 Montpellier 05, FranceEcole Natl Super Chim Montpellier, CNRS, Inst Charles Gerhardt, UMR 5253,AM2N, F-34296 Montpellier 05, France
Racine, Emilie
Monnier, Florian
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Ecole Natl Super Chim Montpellier, CNRS, Inst Charles Gerhardt, UMR 5253,AM2N, F-34296 Montpellier 05, FranceEcole Natl Super Chim Montpellier, CNRS, Inst Charles Gerhardt, UMR 5253,AM2N, F-34296 Montpellier 05, France
Monnier, Florian
Vors, Jean-Pierre
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Bayer CropSci SA, F-69005 Lyon, FranceEcole Natl Super Chim Montpellier, CNRS, Inst Charles Gerhardt, UMR 5253,AM2N, F-34296 Montpellier 05, France
Vors, Jean-Pierre
Taillefer, Marc
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Ecole Natl Super Chim Montpellier, CNRS, Inst Charles Gerhardt, UMR 5253,AM2N, F-34296 Montpellier 05, FranceEcole Natl Super Chim Montpellier, CNRS, Inst Charles Gerhardt, UMR 5253,AM2N, F-34296 Montpellier 05, France
机构:
Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
Univ Chinese Acad Sci, Beijing 100049, Peoples R ChinaChinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
Hu, Dongyan
Li, Mengsun
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Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
Univ Chinese Acad Sci, Beijing 100049, Peoples R ChinaChinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China