Organic Letters · 2017 · 52 citations · 59 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryCross-coupling ReactionsDiversity-oriented SynthesisHeterocyclic ChemistryCarbene Insertion ReactionsChemoselectivity OptimizationCopper-catalyzed CouplingInsertion Selectivity
A highly efficient P–H insertion of α-imino copper carbene into H-phosphine oxides, leading to 3-phosphinoylindoles with a broad substrate diversity and good chemoselectivity, is established. This methodology provides a rapid and efficient approach for the C (sp 2 )–P bond formation via the P–H insertion strategy. The stereoselective P–H insertion of α-imino copper carbene represents a unique example of asymmetric P–H insertion, affording P-stereogenic 3-phosphinoylindoles with high stereoselectivities.
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Recent studies on the reactions of α-diazocarbonyl compounds
Zhenhua Zhang, Jianbo Wang · Tetrahedron · 2008 · 765 citations