2022
DOI: 10.1039/d1ob02443d
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Regioselective synthesis of 6-nitroindole derivatives from enaminones and nitroaromatic compounds via transition metal-free C–C and C–N bond formation

Abstract: Few methods are known for the synthesis of nitroindole derivatives. A simple and practical Cs2CO3-promoted method for the synthesis of 6-nitroindole derivatives from enaminones and nitroaromatic compounds has been developed....

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Cited by 4 publications
(2 citation statements)
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References 85 publications
(27 reference statements)
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“…Very recently, Ge et al recommended a practical protocol for 6-nitroindole derivatives 79 starting from easily accessible enaminones 78 and nitroaromatic compounds 77 . 82 The transformation was promoted by Cs 2 CO 3 in chlorobenzene solvent. A series of N -substituted-3-aminocyclohex-2-enones possessing electro-donating/withdrawing groups (Me, t Bu, OMe, OEt, F, Cl, CF 3 , etc. )…”
Section: Base-catalyzed Synthesismentioning
confidence: 99%
“…Very recently, Ge et al recommended a practical protocol for 6-nitroindole derivatives 79 starting from easily accessible enaminones 78 and nitroaromatic compounds 77 . 82 The transformation was promoted by Cs 2 CO 3 in chlorobenzene solvent. A series of N -substituted-3-aminocyclohex-2-enones possessing electro-donating/withdrawing groups (Me, t Bu, OMe, OEt, F, Cl, CF 3 , etc. )…”
Section: Base-catalyzed Synthesismentioning
confidence: 99%
“…So, the photochemical regioselective C–N cross-coupling reactions are of great interest in organic synthesis. 16…”
mentioning
confidence: 99%