Technology Process of 6-phenyl-15H-benzo[a]naphtho[1',2':11,12]chryseno[5,6-c]carbazole
There total 8 articles about 6-phenyl-15H-benzo[a]naphtho[1',2':11,12]chryseno[5,6-c]carbazole which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
silver tetrafluoroborate; chloro[2-dicyclohexyl(2′,4′,6′-triisopropylbiphenyl)phosphine]gold(I);
In
ethanol;
at 80 ℃;
for 21h;
Inert atmosphere;
DOI:10.1021/jo2018119
- Guidance literature:
-
Multi-step reaction with 8 steps
1: copper(l) iodide; bis(benzonitrile)palladium(II) dichloride; tri-tert-butyl phosphine; diisopropylamine / tetrahydrofuran / 20 °C
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 °C
3: copper(l) iodide; bis(benzonitrile)palladium(II) dichloride; tri-tert-butyl phosphine; diisopropylamine / tetrahydrofuran / 16 h / 60 °C / Inert atmosphere
4: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 0 °C
5: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / tetrahydrofuran / 5.5 h / 20 °C / Inert atmosphere
6: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 0 °C
7: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / tetrahydrofuran / 6 h / 20 °C / Inert atmosphere
8: silver tetrafluoroborate; chloro[2-dicyclohexyl(2′,4′,6′-triisopropylbiphenyl)phosphine]gold(I) / ethanol / 21 h / 80 °C / Inert atmosphere
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; bis(benzonitrile)palladium(II) dichloride; silver tetrafluoroborate; tri-tert-butyl phosphine; chloro[2-dicyclohexyl(2′,4′,6′-triisopropylbiphenyl)phosphine]gold(I); tetrabutyl ammonium fluoride; triethylamine; diisopropylamine;
In
tetrahydrofuran; ethanol;
1: Sonogashira coupling / 3: Sonogashira coupling / 5: Sonogashira coupling / 7: Sonogashira coupling;
DOI:10.1021/jo2018119
- Guidance literature:
-
Multi-step reaction with 7 steps
1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 °C
2: copper(l) iodide; bis(benzonitrile)palladium(II) dichloride; tri-tert-butyl phosphine; diisopropylamine / tetrahydrofuran / 16 h / 60 °C / Inert atmosphere
3: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 0 °C
4: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / tetrahydrofuran / 5.5 h / 20 °C / Inert atmosphere
5: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 0 °C
6: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / tetrahydrofuran / 6 h / 20 °C / Inert atmosphere
7: silver tetrafluoroborate; chloro[2-dicyclohexyl(2′,4′,6′-triisopropylbiphenyl)phosphine]gold(I) / ethanol / 21 h / 80 °C / Inert atmosphere
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; bis(benzonitrile)palladium(II) dichloride; silver tetrafluoroborate; tri-tert-butyl phosphine; chloro[2-dicyclohexyl(2′,4′,6′-triisopropylbiphenyl)phosphine]gold(I); tetrabutyl ammonium fluoride; triethylamine; diisopropylamine;
In
tetrahydrofuran; ethanol;
2: Sonogashira coupling / 4: Sonogashira coupling / 6: Sonogashira coupling;
DOI:10.1021/jo2018119