Organic & Biomolecular Chemistry · 2011 · 34 citations · 38 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistryStructure-activity RelationshipsSynthetic Medicinal ChemistryCross-coupling ReactionsHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisBuilding Block MethodologyCarbazole ChemistryCarbazole SynthesisSonogashira CouplingSuzuki - Miyaura Coupling
A new synthetic pathway towards 2,8-difunctionalised indolo[3,2-b]carbazoles was investigated. The presented method offers a short and high yielding route towards 2,8-dibromo-5,11-dihexyl-6,12-diphenyl-indolo[3,2-b]carbazole. It is demonstrated that the latter compound is a versatile building block, enabling the synthesis of a number of previously unreported 5,11-dialkyl-6,12-diphenyl-indolo[3,2-b]carbazoles in moderate to good yields, using Suzuki and Sonogashira cross-coupling reaction. Furthermore it is shown that 2,8-dibromo-5,11-dihexyl-6,12-diphenyl-indolo[3,2-b]carbazole can be easily formylated, giving rise to the 2,8-diformyl-5,11-dihexyl-6,12-diphenyl-indolo-[3,2-b]carbazole. The latter compound was successfully subjected to condensation reactions.
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The Chemistry of Conducting Polythiophenes
Richard D. McCullough · Advanced Materials · 1998 · 1.5K citations
Catalytic cross-coupling reactions in biaryl synthesis
Stephen P. Stanforth · Tetrahedron · 1998 · 952 citations