Organic Letters · 2003 · 31 citations · 8 references
Natural SciencesChemistryCatalysisOrganic ChemistryOrganic SynthesisAmine FunctionalizationCross CouplingCross-coupling CatalysisGrignard Reagent SynthesisHeterocycle FunctionalizationPyrrole ChemistryPyrrole Synthesis
[reaction: see text] N-Phenylsulfonylpyrrole 1 is magnesiated by treatment with isopropylmagnesium chloride and catalytic diisopropylamine. Reaction with various electrophiles, including palladium-catalyzed aryl- and heteroaryl cross-coupling, provides 2-substituted phenylsulfonylpyrroles in moderate to good yields.
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Regioselective synthesis of acylpyrroles
Masatoshi Kakushima, Pierre Hamel, Richard Frenette et al. · The Journal of Organic Chemistry · 1983 · 200 citations
Iltifat Hasan, Edmund R. Marinelli, Li-Ching Chang Lin et al. · The Journal of Organic Chemistry · 1981 · 160 citations
Thomas J. Tolbert, Chi‐Huey Wong · Angewandte Chemie International Edition · 2002 · 144 citations
New Syntheses of Substituted Pyridines via Bromine–Magnesium Exchange
François Trécourt, Gilles Breton, Véronique Bonnet et al. · Tetrahedron · 2000 · 131 citations