Publication | Closed Access
Acid‐Free Synthesis of Carbazoles and Carbazolequinones by Intramolecular Pd‐Catalyzed, Microwave‐Assisted Oxidative Biaryl Coupling Reactions – Efficient Syntheses of Murrayafoline A, 2‐Methoxy‐3‐methylcarbazole, and Glycozolidine
84
Citations
59
References
2009
Year
Murrayafoline AEngineeringOrganic ChemistryChemistryHeterocycle ChemistryOxygenated CarbazolesChemical EngineeringDiversity Oriented SynthesisIntramolecular Pd‐catalyzedEfficient MethodologyCross-coupling ReactionDerivativesBiochemistryDiversity-oriented SynthesisCatalysisAcid‐free SynthesisSynthesis MethodNew ProtocolBiomolecular EngineeringNatural SciencesSynthetic Chemistry
Abstract A mild and efficient methodology for the synthesis of oxygenated carbazoles from diarylamines under non‐acidic conditions was developed, based on a palladium‐catalyzed, microwave‐assisted double C–H bond activation process. This new protocol was successfully applied to the synthesis of three naturally occurring carbazoles, namely murrayafoline A, 2‐methoxy‐3‐methylcarbazole, and glycozolidine. The scope of the reaction was also expanded to include the synthesis of benzo fused carbazolequinones.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
| Year | Citations | |
|---|---|---|
Page 1
Page 1