Chemical Science · 2013 · 161 citations · 39 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryNatural Product DerivatizationTyrosine Kinase InhibitorsCarbazole ChemistryCarbazole SynthesisChk1 SignalingIndole ChemistryIndole DerivativesIndole SynthesisMedicinal Chemistry ApplicationsReaction Mechanism Elucidation
We have developed a Pd–Cu–Ag trimetallic system that can convert indoles to carbazoles using electron-deficient alkenes as two-carbon units. Investigation of the reaction mechanism revealed that this one-shot indole-to-carbazole π-extension is likely to proceed through the sequence of (i) Pd/Cu-catalyzed indole C–H alkenylation, (ii) Ag-promoted Diels–Alder reaction and dehydrogenative aromatization. The successful one-pot synthesis of a granulatimide derivative, an interesting class of Chk1 kinase inhibitor, highlights the potential of the present reaction for further development and applications.
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Neil P. Grimster, Carolyn Gauntlett, Christopher R. A. Godfrey et al. · Angewandte Chemie International Edition · 2005 · 635 citations
Alfonso García‐Rubia, Ramón Goméz Arrayás, Juan C. Carretero · Angewandte Chemie International Edition · 2009 · 341 citations
Recent trends in the synthesis of carbazoles: an update
Joyeeta Roy, Amit Kumar Jana, Dipakranjan Mal · Tetrahedron · 2012 · 277 citations