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  • Synthesis of phenanthridinones via palladium-catalyzed C(sp2)-H aminocarbonylation of unprotected o-arylanilines.

Synthesis of phenanthridinones via palladium-catalyzed C(sp2)-H aminocarbonylation of unprotected o-arylanilines.

Chemical communications (Cambridge, England) (2012-11-22)
Dongdong Liang, Ziwei Hu, Jiangling Peng, Jinbo Huang, Qiang Zhu
ZUSAMMENFASSUNG

An efficient synthesis of free (NH)-phenanthridinones through Pd-catalyzed C(sp(2))-H aminocarbonylation of unprotected o-arylanilines under an atmospheric pressure of CO has been developed. Some ortho heteroarene substituted anilines as well as N-alkyl protected o-arylanilines are also suitable substrates for this C-H aminocarbonylation reaction.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Anilin, ACS reagent, ≥99.5%
Sigma-Aldrich
Anilin -hydrochlorid, ≥99%
Sigma-Aldrich
Anilin, ReagentPlus®, 99%
Sigma-Aldrich
Anilin-15N, 98 atom % 15N
Supelco
Anilin, analytical standard
Supelco
Anilin -Lösung, certified reference material, 5000 μg/mL in methanol
Sigma-Aldrich
Anilin-1-13C, 99 atom % 13C
Sigma-Aldrich
Anilin-4-13C, 99 atom % 13C